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698 Cards in this Set

  • Front
  • Back
Vitamin A deficiency
night blindness, dry skin
Vitamin B1 (thiamine) def
beriberi (polyneuritis, dilated cardiomyopathy, high output CHF, edema), Wernicke-Korsakoff syndrom
Vitamin B2 (riboflavin) def
angular stomatitis, cheilosis, corneal vascularization
Vitamin B3 (niacin) def
pellagra (diarrhea, dermatitis, dementia)
Vitamin B5 (pantothenate) def
dermatitis, enteritis, alopecia, adrenal insufficiency
Vitamin B6 (pyridoxine) def
convulsions, hyperirritability; required during administration of INH
Vitamin B12 (cobalamin) def
macrocytic, megaloblastic anemia, neurologic symptoms (optic neuropathy, subacute combined degneration, paresthesias), glossitis
Vitamin C def
scurvy (swollen gums, bruising, anemia, poor wound healing)
Vitamin D def
rickets in children, osteomalacia in adults (soft bones), hypocalcemic tetany
Vitamin E def
increased fragility of RBCs
Vitamin K def
neonatal hemorrhage, increase PT and aPP, normal BT
biotin def
dermatitis, enteritis, can be caused by ingestion of raw eggs or antibiotic use
Folic acid def
MOST COMMON VIT DEFICIENCY IN US; sprue, macrocytic, megaloblastic anemia without neuro signs
Mg def
weakness, muscle cramps, exacerbation of hypocalcemic tetany, CNS hyperirritability leading to tremors and choreoathetoid movement
Selenium def
Keshan disease (cardiomyopathy)
unstable angina
angina is new, worsening or occurs at rest
Antihypertensive for a diabetic pt with proteinuria
ACE I
Beck's triad for cardiac tamponade
hypotension, distant heart sounds and elevated JVD
drugs that slow AV transmission
beta blockers, digoxin, calcium channel blockers
hypercholesterolemia tx that causes flushing and pruritis
niacin
tx for a-fib
anticoagulation, rate control, cardioversion
tx for v-fib
immediate cardioversion
autoimmune complication occurring 2-4 weeks post MI
Dressler's syndrome: fever, pericarditis, increased ESR
IV drug use with JVD and holosystolic murmur at left sternal border...tx?
tx existing heart failure and replace tricuspid valve
Diagnostic test for hypertrophic cardiomyopathy
echocardiogram (showing thickened left ventricular wall and outflow obstruction)
a fall in systolic BP of > 10mmHg with inspiration
pulsus paradoxus (seen in cardiac tamponade)
low-voltage, diffuse ST segment elevation
classic ECG finding in pericarditis
HTN =
BP > 140/0 on three separate occasions two weeks apart
8 surgically correctable causes of HTN
renal artery stenosis, coarctation of the aorta, pheochromocytoma, Conn's syndrome, Cushings, unilateral renal parenchymal disease, hyperthyroidism and hyperparathyroidism
indications for surgical repair of abd aortic aneurysm
> 5.5 cm, rapidly enlarging, symptomatic, or ruptured
Tx for acute coronary syndrome
morphine, O2, sublingual nitroglycerin, AA, IV beta blockers, heparin
metabolic syndrome
abd obesity, high TGs, low HDL, HTN, insulin resistance, prothrombotic or pro-inflam states
target LDL in pt with diabetes
< 70
signs of active ischemia during stress testing
angina, ST-segment changes on EKG or decreased BP
ECG findings suggesting MI
ST elevation (depression means ischemia), flattened T waves and Q waves
young pt has angina at rest with ST segment elevation, cardiac enzymes are nl
prinzmetals angina
common symptoms with silent MIs
CHF, shock, and altered mental status
diagnostic test for pulm embolus
V/Q scan
reverses effects of heparin
protamine
coagulation parameter affected by warfarin
PT
endocarditis prophylaxis regimens
oral surgery - amoxicillin
GI/GU procedures: ampicillin and gentamicin before and amoxicillin after
6 P's of ischemia due to peripheral vascular disease
pain, pallor, pulselessness, paralysis, parethesia and poikilothermia (cold)
Virchow's triad
stasis, hypercoagulability and endothelial damage
most common cause of HTN in young women
OCPs
most common cause of HTN in young men
excessive EtOH
"stuck on" appearance
seborrheic keratosis
red plaques with silvery-white scales and sharp margins
psoriasis
most common type of skin cancer; lesion is pearly colored papule with a translucent surface and telangiectasias
basal cell carcinoma
honey crusted lesions
impetigo
febrile patient with history of diabetes presents with a red, swollen, painful lower extremity
cellulitis
+ Nikolsky's sign
pemphigus vulgaris
- Nikolsky's sign
bullous pemphigoid
55 year old obese pt presents with dirty, velvety patches on back of neck
acanthosis nigricans; check fasting blood sugar to r/o diabetes
Dermatomal distribution
varicella zoster
flat-topped papules
lichen planus
iris-like target lesions
erythema multiforme
presents with a herald patch, Christmas-tree pattern
pityriasis rosea
16 yo presents with an annular patch of alopecia with broken-off, stubby hairs
alopecia areata (autoimmune process)
pinkish, scaling, flat lesions on the chest and back; KOH prep has a "spaghetti and meatballs" appearance
pityriasis versicolor
four characteristics of nevus suggestive of melanoma
asymmetry, border irregularity, color variation, large diameter
premalignant lesion from sun exposure that can lead to squamous cell carcinoma
actinic keratosis
"dewdrop on a rose petal"
lesions of primary varicella
"cradle cap"
seborrheic dermatitis...treat with antifungals
associated with Propionibacterium acnes and changes in androgen level
acne vulgaris
painful, recurrent vesicular eruption of mucocutaneous surfaces
herpes simplex
inflammation and epithelial thinning of anogenital area, predominantly in postmenopausal women
lichen sclerosus
exophytic nodules on skin with varying degrees of scaling or ulceration; second most common type of skin cancer
squamous cell carcinoma
induction of p450 enzymes
barbiturates, phenytoin, carbamazepine, rifampin, quinidine, griseofulvin
inhibition of p450 enzymes
cimetidine, ketoconazole, INH, grapefruit, erythromycin, sulfonamides
Metabolism by p450 enzymes
benzos, amide anesthetics, metoprolol, propranolol, nifedipine, phenytoin, quinidine, theophylline, warfarin, barbiturates
increase risk of digoxin toxicity
quinidine, cimetidine, amiodarone, calcium channel blockers
competition for albumin binding sites
warfarin, asa, phenytoin
blood dyscrasias
ibuprofen, quinidine, methyldopa, chemo agents
hemolysis in G6PD deficient patients
sulfonamides, INH, ASA, ibuprofen, nitrofurantoin, primaquine, pyrimethamine, chloramphenicol
Gynecomastia
spironolactone, estrogens, digitalis, cimetidine, chronic alcohol use, ketoconazole
stevens johnson syndrome
ethosuximide, sulfonamide
photosensitivity
tetracycline, amiodarone, sulfonamides
drug induced SLE
procainamide, hydralazine, INH, penicillamine, chlorpromazine, methyldopa, quinidine
three most common causes of fever of unknown origin
infection, cancer, and autoimmune disease
four signs and symptoms of streptococcal pharyngitis
fever, pharyngeal erythema, tonsillar exudate, lack of cough
a nonsuppurative complication of strep infection that is not altered by treatment of primary infection
postinfectious glomerulonephritis
asplenic pts are particularly susceptible to these organisms
encapsulated organisms - pneumococcus, meningococcus, H. flu and Klebsiella
number of bacteria on a clean-catch specimen to diagnose UTI
10 x 5 bacteria/mL
health population susceptible to UTI?
pregnant women...treat aggressively because of potential complications
pt from california or arizona presents with fever, malaise, cough and night sweats...
coccidiodomycosis, Amphotericin B
nonpainful chancre
primary syphilis
"blueberry muffin" rash
rubella
meningitis in neonates...causes? tx?
group B strep, E. coli, Listeria...tx with gentamycin and ampicillin
meningitis in infants...causes? tx?
pneumococcus, meningococcus, H. flu...
tx with cefotaxime and vanco
CSF - nl glucose and lymphocytic predominance
aseptic (viral) meningitis
numerous RBCs in serial CSF samples
subarachnoid hemorrhage
initially presents with pruritic papule with regional lymphadenopathy and evolves into black eschar after 7-10 days...
cutaneous anthrax, tx with penicillin G or ciprofloxacin
findings in tertiary syphilis
tabes dorsalis, general paresis, gummas, argyll robertson pupils, aortitis, aortic root aneurysms
cold agglutinins
mycoplasma
24 year old male with soft white plaques on tongue and back of throat
candidal thrush...workup should include HIV...treat with nystatin oral suspension
begin PCP proph in HIV + patient at what CD4 count?
MAC prophylaxis?
PCP - < 200 (with TMP-SMX)
MAC - <50-100 (with clarithromycin/azithromycin)
risk factors for pyelonephritis
pregnancy, vesicoureteral reflux, anatomic anomalies, indwelling catheters, kidney stones
neutropenic nadir postchemo
7-10 days
classic physical findings of endocarditis
fever, heart murmur, Osler's nodes, splinter hemorrhages, Janeway lesions, Roth's spots
aplastic crisis in sickle cell disease
Parvovirus B19
ring-enhancing brain lesions on CT with seizures
taenia solium (cysticercosis)
branching rods in oral infection
actinomyces israelii
painful chancroid
haemophilus ducreyi
dog or cat bite
pasteurella multocida
gardener
sporothrix schenckii
pregnant women with pets
toxoplasma gondii
meningitis in adults
neisseria meningitidis
meningitis in elderly
strep pneumo
alcoholic with pneumonia
klebsiella
'currant jelly' sputum
klebsiella
infection in burn victims
pseudomonas
osteomyelitis from foot wound puncture
pseudomonas
osteomyelitis in sickel cell patients
salmonella
55 year old man who is a smoker and a heavy drinker presents with new cough and flulike symptoms...gram stain shows no organisms; silver stain of sputum shows gram neg rods...dx?
legionella pneumonia
middle aged man presents with acute-onset monoarticular joint pain and bilateral Bell's palsy...dx, tx?
Lyme disease, Ixodes tick, doxycycline
pt develops endocarditis 3 weeks after receiving prosthetic heart valve...organism?
staph aureus or staph epidermidis
Xeroderma pigmentosum (a/cancer)
squamous cell and basal cell carinoma of the skin
Gastric adenocarcinoma is a/w
chronic atrophic gastritis, pernicious anemia, postsurgical gastric remnants
Astrocytoma and cardiac rhabdomyoma a/w
tuberous sclerosis (facial angiofibroma, seizures, mental retardation)
Actinic keratosis a/w
squamous cell carcinoma of the skin
Barret's esophagus (chronic GI reflux)
a/w esophagel adenocarcinoma
Plummer Vinson Syndrome a/w
first: Plummer Vinson syndrome is atrophic glossitis, eophageal webs, anemia...all due to iron deficiency

a/w squamous cell carcinoma of the esophagus
ulcerative colitis a/w
colonic adenocarcinoma
paget's disease of the bone a/w
secondary osteosarcoma and fibrosarcoma
immunodeficiency states a/w
malignant lymphomas
AIDS a/w (neoplasm)
aggressive malignant NHLs and Kaposi's sarcoma
autoimmune diseases (like myastenia) a/w
benign and malignant thymomas
acanthosis nigricans a/w
visceral malignancy (stomach, lung, breast and uterus)
dysplastic nevus a/w
malignant melanoma
four causes of microcytic anemia
thalassemia, iron deficiency, anemia of chronic disease and sideroblastic anemia
precipitants of hemolytic crisis in patients with G6PD deficiency
sulfonamides, antimalarial drugs and fava beans
most common inherited cause of hypercoagulability
factor V Leiden mutation
most common inherited hemolytic anemia
hereditary spherocytosis
diagnostic test for hereditary spherocytosis
osmotic fragility test
pure RBC aplasia
diamond-blackfan anemia
Fanconi's anemia
anemia a/w absent radii and thumbs, diffuse hyperpigmentation, cafe-au-lait spots, microcephaly and pancytopenia
meds and viruses that lead to aplastic anemia
chloramphenicol, sulfonamides, radiation, HIV, chemotherpeutic drugs, hepatitis, parvo B19 and EBV
how to distinguish polycythemia vera from secondary polycythemia
both have increased hematocrit and RBC mass, but polycythemia vera has normal O2 sats and low EPO levels
TTP pentad!!!
fever, renal failure, anemia, thrombocytopenia and neurologic abnls
HUS triad
anemia, thrombocytopenia and acute renal failure
treatment for TTP
emergent large volume plasmapheresis, corticosteroids and antiplatelet drugs
tx for ITP in kids
usually resolves spontaneously, may require IVIG and/or corticosteroids
changes in DIC
elevated fibrin split products and D-dimer
decreased platelets, fibrinogen and hematocrit
14 year old girl with prolonged bleeding after dental surgery and with menses...nl PT, nl or increased PTT, increased bleeding time...dx?
von Willebrand's disease, treat with desmopressin, FFP or cryoprecipitate
60 year old AA male with bone pain...w/u for MM may reveal?
monoclonal gammopathy, bence jones proteinuria, "punched out" lesions on x-ray of skull and long bones
reed sternberg cells
hodgkins lymphoma
microcytic anemia with decreased serum iron, decreased TIBC and normal or increased ferritin
anemia of chronic disease
microcytic anemia with decreased serum iron, decreased ferritin and increased TIBC
iron deficiency anemia
80 yo male with fatigue, lymphadenopathy, splenomegaly and isolated lymphocytosis...wtf?
CLL
late, life-threatening complication of CML
blast crisis (fever, bone pain, splenomegaly, pancytopenia)
auer rods on blood smear
AML
AML subtype associated with DIC
M3
elec changes in tumor lysis syndrome
dec calcium, increased K, increased phosphate and increased uric acid
treatment for AML M3
retinoic acid
heinz bodies?
intracellular inclusions seen in thalassemia, G6PD def and post-splenectomy
Glanzmann's thrombasthenia
AR disorder with defect in GPIIb/IIIa platelet receptor and decreased platelet aggregation
virus associated with aplastic anemia in pts with sickle cell
parvovirus B19
25 year old AA male with sickle cell anemia has sudden onset bone pain...management?
O2, analgesia, hydration, and, if severe, transfusion
significant cause of morbidity in thalassemia patients...tx?
iron overload; use deferoxamine
elevated alpha feto protein
open neural tube defects (anencephaly, spina bifida), abdominal wall defects (gastroschisis, omphalocele), multiple gestation, incorrect gestational age, fetal death and placental abnormalities (placental abruption)
abnormally low alpha fetoprotein
should do amniocentesis and karyotyping to rule out chromosomal abnormalities
quad screen
alpha fetoprotein, inhibin A, estriol and beta-hCG
decreased AFP, decreased estriol, decreased beta-hCG and decreased inhibin A
trisomy 18
decreased AFP, decreased estriol, increased beta-hCG and increased inhibin A
trisomy 21
reasons for amniocentesis
>35 years old, conjuction with abnl quad screen, Rh-sensitized pregnancy to obtain fetal blood type or detect fetal hemolysis, to evaluate fetal lung maturity via a lecithin-sphingomyelin ratio >2.5 or to detect presence of phosphatidylglycerol (done during 3rd trimester)
chorionic villous sampling
can be done earlier - 10-12 weeks gestation...better diagnostic accuracy

dis: risk of fetal loss and inability to diagnose neural tube defects is 0.5% - 1% higher than with amnio

limb defects a/w CVS performed earlier than 9 weeks
percutaneous umbilical blood sampling
gett blood from umbilical vessels...used to diagnose fetal hemolytic disease and fetal infection
category A drugs (preg)
fine...no harm...ex: vit C
cat B drugs (preg)
no risk in animal studies...ampicillin
cat C drugs (preg)
drugs given only if potential benefit justifies potential risk to fetus...zidovudine
Cat D drugs (preg)
there are risks, but benefits from use in pregnant women may be acceptable despite the risk...PHENYTOIN
cat X drugs (preg)
just dont do it...no way.

isoretinoin
fetal alcohol syndrome
growth restriction before and after birth, MR, midfacial hypoplasia, renal and cardiac defects...6 drinks/day have 40% risk
androgens/test der in pregnancy
virilization of females, advanced genital dev in males
ACE-I in preg
can cause fetal renal tubular dysplasia and neonatal renal failure, oligohydramnios, IUGR, lack of cranial ossification
coumadin in preg
BAD

nasal hypoplasia and stippled bone epiphyses, develop delay, IUGR, opthalmologic abnl
Carbamazepine in preg
neural tube defects, fingernal hypoplasia, microcephaly, DD and IUGR
folic acid antagonists in preg (methotrexate, aminopterin)
increased spontaneous abortion
cocaine in preg
bowel atresias in fetus, congenital malfms of heart, limbs, face and GU tract; microcephaly; IUGR, cerebral infarction
DES in preg
clear cell adenocarcinoma of vagina or cervix, vaginal adenosis, abnl of cervix and uterus or testes, possible infertility
Lead in preg
increase spont abortion rates, stillbirths
Lithium in preg
congenital heart disease (Ebsteins anomaly)
organic mercury in preg
cerebral atrophy, microcephaly, MR, spasticity, seizures and blindness
Phenytoin in preg
IUGR, MR, microcephaly, dysmorphic craniofacial features, cardiac defects fingernail hypoplasia
Radiation in preg
microcephaly, MR, < 0.05 Gy to the fetus has no teratogenic risk
Streptomycin and kanamycin in preg
hearing loss, CN VIII damage
tetracycline in preg
permanent yellow-brown discoloration of deciduous teeth, hypoplasia of tooth enamel
Thalidomide in preg
bilateral limb deficiencies, anotio and microtia, cardiac and GI abnormalities
Trimethadione and paramethadione in preg
cleft lip and cleft palate, cardiac defects, microcephaly, MR
Valproic acid in preg
neural tube defects (spina bifida), minor craniofacial defects
Vitamin A in preg
increased SAB rate, microtia, thymic agenesis, CV defects, craniofacial dysmorphism, microphthalmia, cleft lip or cleft palate, MR
CMV in preg
can cause in fetus: microcephaly, hydrocephaly, chorioretinitis, cerebral calcifications, IUGR, microphthalmos, MR and hearing loss

THE MOST COMMON CONGENITAL INFECTION
Rubella in preg
to fetus: microcephaly, MR, cataracts, hearing loss, congenital heart disease

do NOT give immunization in pregnancy...live attenuated vaccine (no evidence of it doing sh*t, but dont give it still)
Syphilis in preg
to fetus: fetal hydrops (severe), abnormalities of skin, teeth and bones (mild)
Toxo in preg
to fetus: microcephaly, hydrocephaly, cerebral calcifications, chorioretinitis

transmitted via raw meat or through exposure to infected cat feces
Varicella in preg
to fetus: skin scarring, chorioretinitis, cataracts, microcephaly, hypoplasia of hands and feet, muscle atrophy
Bishop score
to see if cervix is favorable for both spontaneous and induced labor

dilation, effacement, station, cervical position and cervical consistency...> 8 is ready.
early deceleration
apparent, gradual (onset to nadir less than 30sec) decrease in FHR with return to baseline that mirrors uterine contraction

causes: head compression from uterine contraction
late deceleration
gradual onset decrease in FHR with return to baseline whose onset, nadir and recovery occur after the beg, peak and end of uterine ctx.

causes: uteroplacental insufficiency and fetal hypoxemia
variable deceleration
an abrupt decrease in FHR below baseline lasting more than 15 sec but less than 2 min

cause: umbilical cord compression (most often secondary to oligohydramnios)
bradycardia baseline
FHR below 110

causes: congenital heart malformations, severe hypoxia (2/2 uterine hyperstimulation, cord prolapse and rapid fetal descent)
Tachycardia, FHR
FHR > 160...

causes: hypoxia, maternal fever and anemia
BPP (biophysical profile)
5 parameters: breathing, fetal tone, movement, amniotic fluid volume and NST

8-10 is reassuring for fetal well being

6 is equivocal (most term preg)

0-4 is extremely worrisome for fetal asphyxia and strong consideration should be given for immediate delivery
modified BPP
combines NST with the amniotic fluid index...considered normal with reactive NST and an AFI > 5cm
contraindications for regional anesthesia in preggers
refractory mat hypotension, maternal coagulopathy, mat use of heparin within 12 hours, untreated maternal bacteremia, skin infection over needle site and increased ICP caused by a mass lesion
maternal complications of pregestationl DM
DKA (1) and HHNK (2), preeclampsia/eclampsia, cephalopelvic disproportion, preterm labor, infection, polyhydramnios, postpartum hemorrhage, maternal mortality
fetal complications of maternal pregestational DM
macrosomia, cardiac and renal defects, neural tube defects (sacral agenesis), hypocalcemia, polycythemia, hyperbilirubinemia, IUGR, hypoglycemia with hyperinsulinemia, RDS, birth injury (shoulder dystocia), perinatal mortality
BP meds NOT to give in pregnancy
ACE-I or diuretics...

ACE-I can lead to uterine ischemia and diuretics can aggravate low plasma volume to the point of uterine ischemia
complications a/w preeclampsia
prematurity, fetal distress, stillbirth, placental abruption, seizure, DIC, cerebral hemorrhage, serour retinal detachment, fetal/maternal death
severe preeclampsia
BP > 160/110
renal: proteinuria, >5gm/24hr
cerebral: HA, somnolence
Visual changes: blurred vision, scotomata
hyperactive reflexes/clonus
Hemolysis, elevated liver enzymes, thrombocytopenia (HELLP syndrome)

give mag sulfate for prevention of seizures...watch out for toxicity - loss of DTRs, resp paralysis, coma...tx toxicity with IV calcium gluconate
risk factors for placenta previa
prior C-sections, grand multiparous, advanced maternal age, multiple gestation, prior placenta previa
complications of placenta previa
increased risk of placenta accreta, vasa previa (fetal vessels crossing internal os)

preterm delivery, premature rupture of membranes, IUGR and congenital anomalies

recurrence risk 4-6%
oligohydramnios
AFI < 5cm

etiologies: fetal urinary tract abnl (renal agenesis, GU obstruction), chronic uteroplacental insufficiency and ROM

a/w 40-fold increase in perinatal mortality; other complications include musculoskeletal abnormalities (eg clubfoot, facial distortion), pulmonary hypoplasia, umbilical cord compression and IUGR
polyhydramnios
AFI >20

etiologies include: maternal DM, multiple gestation, isoimmunization, pulmonary abnormalities (eg cystic lung abnl), fetal anomalies (eg duodenal atresia, tracheoesophageal fistula, anencephaly) and twin-twin transfusion syndrome

complications: preterm labor, fetal malpresentation, cord prolapse
gestational trophoblastic disease

COMPLETE MOLES
usually result from sperm fertilization of an empty ovum

46XX - paternally derived
Incomplete moles
occur when normal ovum is fertilized by two sperm (or a haploid sperm that duplicates its chromosomes), contains fetal tissue

69XXY
history of ladies with gestational troph. dz
first trimester uterine bleeding, hyperemesis gravidum, preeclampsia/eclampsia at < 24 weeks, uterine size greater than dates

no fetal HB detected, pelvic exam with enlarged ovaries (bilateral theca-lutein cysts) or expulsion of grapelike molar clusters

risk factors: extremes of age, less than 20, more than 40, deficient in folate or beta-carotene and blood group
diagnosis of GTD
markedly increased b-hCG (greater than 100,000)..."snowstorm" on US...

CXR: may have lung mets; D&C reveals cluster of grapes tissue
tx of GTD
follow beta hCG, prevent pregnancy for one year

tx malignancy with chemo (methotrexate or dactinomycin) and residual uterine disease with hysterectomy; chemo and irradiation are cool/good
complications of GTD
molar pregnancy may progress to malignant GTD...including invasive moles (10-15%) and choriocarcinoma (2-5%) with pulm mets or CNS mets

may see trophoblastic pulm nodules
to diagnose premature rupture of membranes
sterile speculum exam shows pooling of amniotic fluid in vaginal vault, + Nitrazine paper test (paper turns blue in alkaline amniotic fluid)
+ fern test - ferning pattern is seen under a microscope after amniotic fluid dries on glass slide

U/S to assess AFI

do NOT perform digital vaginal exams in women who are not in labor or for whom labor in not immediately planned
to tx PROM
term: check GBS and fetal presentation, can induce or wait 24-72 hrs

>34-36 wks: labor induction

<32 wks: expectant management with bed rest and pelvic rest

antibxs to prevent infxt prolong latency period in absence of infection

antenatal corticosteroids: to promote fetal lung maturity in absence of intraamniotic infection prior to 32 weeks GA
uterine atony
risk factors: uterine overdistention, exhausted myometrium, uterine infection, conditions interfering with contractions

dx: soft, enlarged, BOGGY uterus (most common cause of PPH...90%)

tx: bimanual uterine massage, oxytocin, methergine (methylergonovine) if not hypertensive, Prostin (PGF2alpha) if not asthmatic
retained placental tissue
another cause of PPH

risk factors: placenta accreta/increta/percreta, placenta previa, uterine leiomyomas, preterm delivery, previous c-section/curettage
primary syphilis
10-60 days post exposure

chancre

can tx primary or secondary: best is penicillin G, if allergic, can use tetracycline and doxycycline
secondary syphilis
4-8wks after appearance of chancre, maculopapular rash (palms and soles); condylomata lata
tertiary syphilis
1-10 years after infection

granulomas (gummas) of the skin and bones, aortitis, neurosyphilis with meningovascular disease, paresis and tabes dorsalis

must tx with penicillin...if allergice, desensitize pt.
herpes genitalis
primary: malaise, myalgias and fever with vulvar burning/pruritis (2-5 days post exposure) followed by vesicular genital lesions (3-7 days post exposure)...shallow, painful ulcers with a red border

HSV 2 (85% genital lesions)

Tzanck smear...presence of multinucleated giant cells with eosinophilic inclusion...viral culture is most sensitive

tx: sitz baths and dryer...acyclovir, famciclovir or valacyclovir for primary or for suppressive tx for frequent recurrences
chancroid
painful, nonindurated, purulent, hemorrhagic ulcers with painful inguinal lymphadenopathy

h. ducreyi

tx: ceftriaxone, azithromycin, erythromycin or cipro
lymphogranuloma venereum
primary: presents with painless, transient papule or shallow ulcer that can go unnoticed

secondary: inguinal syndrome - painful enlargement and inflammation of inguinal nodes with fever, malaise, HA and loss of appetite

tertiary: anogenital syndrome, anal pruritis with discharge, proctocolitis, rectal stricture, rectovaginal fistula and elephantiasis

L-serotype Chlamydia trachomatis

tx: doxycycline 100mg BID x 21 days
granuloma inguinale
raised, firm lesions

Calymmato-bacterium granulomatis

tx: doxy, bactrim or cipro
condylomata acuminata (genital warts)
raised cauliflower like lesions...in immunocompromised pts

HPV, HPV 6 and HPV 11

tx: surgical, chemical (TCA, podophyllin, 5-FU, podofilox), immunologic imiquimod)
molluscum
poxviridae

tx with desiccation, cryotherapy, curettage or imiquimod
inpt antibiotics for PID
1. cefoxitin or cefotetan and doxycycline x 14 days
2. clinda and gent x 14 days
outpt tx for PID
1. cefoxitin with probenecid x 1 dose
2. ceftriaxone IM and doxycycline
3. ofloxacin and metronidazole
trichomonas
protozoal flagellates affect the vagina, skene's duct and lower urinary tract...

STRAWBERRY PETECHIAE in upper vagina/cervix

d/c: profuse, malodorous, yellow-green, frothy

wet mount: motile trichomonads (slightly larger than WBCs)

tx: single dose PO metronidazole or tinidazole

complications: chorioamnionitis/endometritis, infection, preterm delivery, miscarriage, PID, cellulitis when invasive procedures done
risk factors for yeast infections
diabetes, broad-spectrum antibiotic use, pregnancy steroids, HIV, OCP use, IUD use, young age at first intercourse, increased freq of intercourse

(avoid oral azoles in pregnancy)
vulvar cancer
a/w HPV types 16, 18 and 31, diabetes, obesity, HTN, CV dz and immunosuppression

VIN (vulvar intraepithelial neoplasia)...dx with punch biopsy

VIN III: carcinoma in situ

about 87% are squamous cell carcinomas and 6% malignant melanomas...remainder are basal cell carcinoma and Paget's disease

safe sex can help prevent this
ovarian cancer
nulliparity, breast cancer, family history...

OCP use is protective.

CA-125 for epithelial cancers
AFP and b-hCG for germ cell cancers

tx: TAH/BSO and peritoneal washing for cytology w or w/o pelvic and aortic node sampling, tumor debulking, chemo

prevention: OCPs, prophylactic BSO with fm history

most common cause of death is bowel obstruction
more on ovarian tumors
pats with first-deg relative have 5% lifetime risk...with >2 relatives, risk is 7%

BRCA1 has 45% lifetime risk
BRCA2 has 25% lifetime risk

OCPs decrease risk!!!

tumor marker CA-125...used only for progression and recurrence
Lynch II syndrome
hereditary nonpolyposis colorectal cancer (HNPCC) is associated with increased risk of colon, ovarian, endometrial and breast cancer
CA-125 in ovarian tumors
premenopausal women: increased CA-125 may point to benign such as endometriosis

postmenopausal women: increased indicates an increased likelihood that the ovarian tumor is malignant

any palpable ovarian or adnexal mass in a premenarchal or postmenopausal patient is suggestive of ovarian neoplasm
marker for ovarian epithelial tumor
CA-125
marker for endodermal sinue ovarian tumor
AFP
marker for ovarian tumor embryonal carcinoma
AFP, hCG
marker for ovarian tumor choriocarcinoma
hCG
marker for ovarian tumor dysgerminoma
LDH
marker for ovarian tumor granulosa cell
inhibin!
stress incontinence
activities that increase intra-abd pressure

etiology: urethral sphincteric insufficiency due to laxity of pelvic floor musculature; common in multiparous women or after pelvic surgery

tx: surgery places bladder neck into app anatomical location;

swab test: greater than 30 degrees with increased intra-abd pressure
urge incontinence
unexpected urge to void, unrelated to position or activity

etiology: detrussor hyperreflexia or sphincter dysfunction 2/2 inflammatory conditions or neurogenic d/o of bladder...

tx: anticholinergics or TCAs

oxybutynin
overflow incontinence
chronic urinary retention

etiology: chronically distended bladder; increased intravesical pressure that just exceeds outlet resistance, allowing small amt of urine to dribble out

tx: place urethral catheter in acute settings

bethanecol and alpha blockers
primary causes of third trimester bleeding
placental abruption and placenta previa
classic U/S and gross appearance of complete hydatidiform mole
snowstorm on U/S, "cluster of grapes" on gross exam
molar pregnancy containing fetal tissue
partial mole
antibiotics with teratogenic effects
tetracycline, fluoroquinolones, aminoglycosides and sulfonamide
shortest AP diameter in pelvis
obstetric conjugate: between sacral promontory and midpoint of symphysis pubis
tx for postpartum hem
uterine massage, if fails, oxytocin
typical antibiotics for group B strep prophylaxis
IV penicillin or ampicillin
term for heaving bleeding during and between menstrual periods
menometrorrhagia
cause of amenorrhea with normal prolactin, no response to estrogen-progesterone challenge, history D&C
Asherman's syndrome
indications for med tx of ectopic preg
stable, unruptured ectopic of <3.5cm at <6wks gestation
med options for endometriosis
OCPs, danazol, GnRH agonists
lap findings in endometriosis
chocolate cysts, powder burns
most common location of ectopic preg
ampulla of oviduct
patient has increased vaginal discharge and petechial patches in upper vagina and cervix
trichomonas vaginitis
most common cause of bloody nipple discharge
intraductal papilloma
breast malignancy presenting as itching, burning and erosion of nipple
Paget's
annual screening for women with strong fm history of ovarian cancer
CA-125 and transvaginal US
30 year old has unpredictable urine loss...med options?
anticholinergics (oxybutynin) or beta-adrenergics (metaproterenol) for urge incontinence
most common cause of female infertility
endometriosis
two consecutive findings of atypical squamous cells of undet significance on pap...f/u?
colposcopy and endocervical curettage
breast cancer type that increases future risk of invasive carcinoma in both breasts
lobular carcinoma in situ
five thoracic causes of immediate death
tension pneumo, cardiac tamponade, open pneumo, massive hemothorax and airway obstruction
always suspect aortic disruption with...
scapular, sternal or first and second rib fractures

CXR: widened mediastinum (>8cm), loss of aortic knob, pleural cap, deviation of trachia and esophagus to the right, depression of left main stem bronchus

get CT or TEE before surgery

aortography is gold standard
asystole
give epinephrine and atropine
v-fib or v-tach
desyn shock then epi then shock then amio or lidocaine then shock then epi

if stable, amiodarone

vasopressin can be given in place of 1st or 2nd dose of epi
pulseless electrical activity
give epi and atropine

causes: hypovolemia, hypoxia, acidosis, hyper/hypokalemia, hypothermia, tablets, tamponade, thromobosis
emergent SVT
unstable: electrical cardioversion

stable: control rate with maneuvers (valsalva, carotid sinus massage or cold stimulus)

if resistant to maneuvers: adenosine
a-fib/flutter tx (ER)
unstable: shock at 100J
stable: rate control with diltiazem or beta blockers, convert rhythm (<48 elect or chemical, >48 need to anticoagulate or do TEE)

dont give nodal blockers if pt has WPW
bradycardia (ER)
symptomatic: atropine and consider dopamine, epi or glucagon

if mobitz II or 3rd degree block present, place transvenous pacemaker
suspect smoke inhalation in...
singed nose hairs, facial burns, hoarseness, wheezing or carbonaceous sputum
fevers before POD 3 are unlikely to be infectious unless...
clostridium or beta-hemolytic streptococci are involved
CATCH 22
cardiac abnormalities
abnormal facies
thymic aplasia
cleft palate
hypocalcemia
22q11 deletion
tetralogy of fallot
pulmonary stenosis, RVH, overriding aorta and VSD

most common cyanotic congenital heart disease in children

risk factors: maternal PKU and CATCH 22 syndromes

"tet spells" - hypoxemic episodes...children often squat for relief (increases systemic vascular resistance)

CXR: "boot shaped" heart with decreased pulmonary vascular markings...EKG with right-axis deviation
breast bud dev age

testicular enlargment age
breast bud dev: btw 8 and 13 years

testicular enlargement btw 9 and 11 years
Trisomy 21
Downs

a/w duodenal atresia, Hirschsprung's and congenital heart disease (most common malformation is AV canal, which includes an ASD and VSD with mitral and tricuspid valve abnormalities 2/2 endocardial cushion defects)

increased risk of ALL and early onset Alzheimer's, increased risk for atlantoaxial (C1-C2) instability
Edward's Syndrome
Trisomy 18

severe MR, rocker-bottom feet, low-set ears, micrognathia, clenched hands and prominent occiput

a/w congenital heart disease, may have horseshoe kidneys

death usually occurs within one year of birth
Patau's syndrome
Trisomy 13

severe MR, microphthalmia, microcephaly, cleft lip/palate, abnormal forebrain structures (holoprosencephaly), "punched out" scalp lesions and polydacyly

a/w congenital heart disease

death usually occurs within one year of birth
Klinefelter's
45, XXY

inactivated X chromosome (Barr body)

one of most common causes of hypogonadism in males

presents with testicular atrophy; eunuchoid body shape; tall, long extremities; gynecomastia and female hair distributions
Turner's
45, XO

most common cause of primary amenorrhea

no barr body

short stature, webbed neck, ovarian dysgenesis and coarctation of aorta...lymphedema of hands and feet in neonatal period

may have horseshoe kidney

buccal smear helpful

normally Turners is 45 XO, but if 45 XY with turners, increased risk of gonadoblastoma - needs prophylactic bilateral gonadectomy
Phenylketonuria
decreased phenylalanine hydroxylase or decreased tetrahydrobiopterin cofactor

screened for at birth - valid only after baby has had protein meal

tyrosine becomes essential and phenylalanine builds up excess phenyl ketones

MR, fair skin, eczema and a musty or mousy urine odor

blonde-haired, blue-eyed infants

a/w increased heart disease

tx: decreased phenylalanine and increased tyrosine in diet, if mom with PKU wants to become pregnant, must restrict diet before conception
Fragile X syndrome
an x-linked defect affecting the methylation and expression of FMR1 gene

second most common cause of genetic mental retardation

presents with macro-orchidism; long face with large jaw; large everted ears and autism

triplet repeat disorder that may show genetic anticipation
Fabry's
x-linked recessive

deficiency of alpha-galactosidase A leads to accumulation of ceramide trihexoside in heart, brain and kidneys...renal failure and increased risk of stroke and MI
Krabbe's dz
autosomal recessive

NO galactosylceramide and galactoside (due to galactosylceramidase deficiency) leads to accumulation of galactocerebroside in brain

optic atrophy, spasticity and early death
Gaucher's dz
AR

deficiency of glucocerebrosidase leads to glucocerebroside accumulation in the brain, liver, spleen and bone marrow (Gaucher's cells have characteristic "crinkled paper" enlarged cytoplasm)

may have hepatosplenomegaly, anemia and thrombocytopenia

type I more compatible with life...does not affect brain
Niemann-Pick dz
AR

deficiency of sphingomyelinase which leads to buildup of sphingomyelin cholesterol in reticuloendothelial and parenchymal cells and tissues

patients with type A die by age of 3
Tay Sachs dz
TAY SAX LACKS HEXOSAMINIDASE

no hexosaminidase leads to GM2 ganglioside accumulation, may appear nl until 3-6 months of age, weakness begins and development slows

exaggerated startle response, death by age 3

cherry red spot on macula

carrier rate is 1/30 Jews of European descent
Metachromatic leukodystrophy
AR

deficiency of arylsulfatase A, accumulation of sulfatide in the brain, kidney, liver and peripheral nerves
Hurler's syndrome
AR

def of alpha-L-iduronidase leads to corneal clouding and MR
Hunter's syndrome
X-linked recessive (hunters need to see...no corneal clouding...to aim at the X.

def of iduronate sulfatase, milder form of Hurler's with no corneal clouding and mild MR
cystic fibrosis
autosomal recessive

mutation in CFTR gene (chloride channel) on chromosome 7 with widespread exocrine gland dysfunction

15% infants have meconium ileus, other GI symptoms include greasy stools and flatulence, pancreatitis, rectal prolapse, esophageal varices and biliary cirrhosis

other sym: type 2 DM, "salty taste", male infertility and unexplained hyponatremia

at risk for fat-soluble vitamin def (vit A, D, E and K) 2/2 malabsorption...may have bleeding symptoms with vit K def
B cell deficiencies (peds)
most common 50%

typicall present AFTER 6 months of age with recurrent sinopulmonary, GI and UTIs with encapsulated organisms (H flu, Strep pneumo, N. meningitidis); treat with IVIG

X-linked agammaglobulinemia (Brutons), common variable immunodeficiency and IgA def
T cell def (peds)
tends to present earlier (1-3 months) with opportunistic and low-grade fungal, viral and intracellular bacterial infections
phagocytic def (peds)
mucous mem infections, abscesses and poor wound healing

infections with catalase + organisms (staph aureus), fungi and gram - enteric org
X-linked agamma-globulinemia (Brutons)
b cell deficiency only in boys

infections with encapsulated pseudomonas, strep pneumo and h. flu

dx/tx: quantitative immunoglobulin levels; if low confirm with B and T cell subsets (no b cells, t cells often high)

absent tonsils and other lymphoid tissues may be a clue

tx with prophylactic antibodies and IVIG
common variable immunodeficiency
immunoglobulin levels drop in 20s and 30s, usually combined B and T cell defect

increase pyogenic upper and lower respiratory infections; increased risk of lymphoma and autoimmune disease

dx/tx: quantitative Ig levels; confirm with B and T cell subsets; treat with IVIG
IgA deficiency
mild, the most common immunodeficiency

usually asymptomatic, recurrent infections

anaphylactic transfusion rxt due to anti-IgA antibodies is a common presentation

sinopulmonary and GI (giardia) - consequence of IgA's role in mucosal barrier protection

dx: quantitative IgA levels; tx infections
Thymic aplasia (DiGeorge)
cardiac, abnl facies, thymic aplasia, cleft palate, hypocalcemia and 22q11 del
defect in dev of 3rd/4th pharyngeal pouch, low set ears, anomolies of great vessels
can present with tetany 2/2 hypocalcemia in first days of life

way increased risk of infections with fungi and PCP

dx: abs lymphocyte count, mitogen stim response, delayed hypersensitivity skin testing

tx: bone marrow transplant and IVIG, PCP prophylaxis, thymus transplantation
Ataxia telangiectasia
combined B and T cell messed up

oculocutaneous telangiectasias and progressive cerebellar ataxia - caused by DNA repair defect

increased incidence of non-Hodgkin's lymphoma, leukemia and gastric carcinoma

no spec tx; may require IVIG, depending on severity of Ig deficiency
Severe combined immunodeficiency (SCID)
severe lack of B and T cells - adenosine deaminase deficiency

severe, frequent bacterial infections, chronic candidiasis and opportunistic infections

tx with bone marrow transplant or stem cell transplant, IVIG...NEEDS PCP PROPHYLAXIS
Wiskott-Aldrich syndrome
x-linked

(think twins at CHOC)

less severe T and B cell dysfunction

ECZEMA, increased IgE/IgA, decreased IgM and THROMBOCYTOPENIA

classic presentation: bleeding, eczema and recurrent otitis media

very increased risk of atopic disorders, lymphoma/leukemia and infection from strep pneu, staph aureus and H flu type b

supportive tx, if severe, bone marrow transplant
Chronic Granulomatous Disease
phagocytic defect

x-linked (2/3) or AR (1/3) with deficient superoxide production by PMNs and macrophages (mutation which causes loss or inactivation of NADPH oxidase)

anemia, lymphadenopathy and hypergammaglobulinemia

intracellular killing is deficient

chronic skin, pulmonary, GI and UTIs; osteomyelitis and hepatitis

infecting organisms are catalase +, increased risk of infection with aspergillus; may have granulomas of the skin and GI/GU tracts

gm stain neutrophils filled with bacteria

dx: abs neutrophil count with neutrophil assays

NITROBLUE TETRAZOLIUM TEST

treat with DAILY TMP-SMX

IFN-gamma can decrease incidence of serious infection; poss bone marrow transplant and gene therapy
newborm with omphalitis with delayed separation of umbilical cord
leukocyte adhesion deficiency

defect in chemotaxis of leukocytes

recurrent skin, mucosal and pulmonary infections

no pus with minimal inflammation in wounds (due to chemotaxis defect); high WBCs in blood; bone marrow transplant is curative
Chediak-Higashi syndrome
phagocytic defect

AR d/o...defect in neutrophil chemotaxis

THIS INCLUDES OCULOCUTANEOUS ALBINISM, NEUROPATHY AND NEUTROPENIA

waaaay increased incidence of overwhelming infections with strep pyogenes, staph aureus and pseudomonas

bone marrow is tx of choice
complement deficiencies
present in children with congenital asplenia or splenic dysfunction (sickle cell disease)...recurrent bacterial infections with encapsulated organisms
C1 esterase deficiency
hereditary angioedema

AD d/o with recurrent episodes of angioedema lasting 2-72 hrs and provoked by stress or trauma

can be life threatening if have airway edema

dx/tx: total hemolytic complement to assess quantity and function of complement...purified C1 esterase and FFP can be used prior to surgery
Terminal complement def (C5-C9)
inability to form membrane attack complex

recurrent meningococcal or gonococcal infections; rarely lupus or glomerulonephritis

give men vaccine and app antibxs
conjunctivitis, rash, adenopathy, strawberry tongue, hands and feet (red, swollen, flaky skin) and fever > 40 for > 5 days
KAWASAKI.

tx with high dose aspirin and IVIG (to prevent aneurysms)

low dose aspirin is then continued, usually for 6 weeks (may use corticosteroids in IVIG refractory cases, not routinely used)
avoid live vaccines in immunocompromised and pregnant pts...
live vaccine: oral polio vaccine, varicella, MMR

(exception: may give MMR and varicella in HIV peeps)
Croup
3 months to 3 years
acute viral inflammatory disease, primarily subglottic space

parainfluenza 1 (most common), 2 and 3, RSV; influenza and adenovirus

bacterial superinfection may progress to tracheitis

hx: prodromal URI symptoms, low-grade fever, mild dyspnea, inspiratory stridor that worsens with agitation, hoarse voice and characteristic barking cough (usually at night)

dx: CLASSIC STEEPLE SIGN FROM SUBGLOTTIC NARROWING - not sens or spec

may need nebulized RACEMIC EPINEPHRINE!
Epiglottitis
supraglottic infection

used to be H. flu, now strep pneumo, nontypable H flu and viral agents

CAN BE LIFE THREATENING

hx: acute-onset high fever, dysphagia, drooling, muffled voice, insp retractions, cyanosis and soft stridor

pts sit with neck hyperextended and chin protruding, leaning forward

must secure airway before looking in!! will see cherry red swollen epiglottis and arytenoids

thumbprint sign

TRUE EMERGENCY - endotracheal intubation or tracheostomy and IV antibiotics (ceftriaxone or cefuroxime)
most common organisms in childhood bact meningitis
Strep pneumo, N. meningitidis (will give petechial rash) and E. coli

(enteroviruses are most common agents in viral meningitis - all ages, risk factors are sinofacial infections, trauma and sepsis)

can give empiric tx: ceftriaxone, vancomycin and ampicillin

neonates should get ampicillin and cefotaxime or gentamycin

older: ceftriaxone and vanco
erythema infectiosum (5th disease)
parvovirus B19

fever absent or low grade

slapped cheek, erythematous, pruritic, maculopapular rash starts on arms and spreads to trunk and legs, WORSENS WITH FEVER AND SUN EXPOSURE

complications: arthritis, hemolytic anemia, encephalopathy, congenital infection a/w fetal hydrops and death

aplastic crisis may be precipitated in children with increased RBC turnover (sickle cell anemia, hereditary spherocytosis) or in those with decreased RBC production (severe iron def)
measles
paramyxovirus

prodrome: low grade fever with cough, coryza and conjunctivitis...koplik's spots on buccal mucosa

rash: head towards feet

complications: otitis media, pneumonia, laryngotracheitis, subacute sclerosing panencephalitis
Rubella
prodrome: asymptomatic...
rash: also starts on face and goes downwards; in contrast with pts with measles, rubella often have low grade fever and do not seem ill
Roseola
HHV 6 (herpes)!

prodrome: acute onset of high fever, no other symptoms for 3-4 days

rash: MACULOPAPULAR RASH APPEARS AS FEVER BREAKS, begins on trunk and spreads to face and extremities

comp: FEBRILE SEIZURES
Hand-foot-and-mouth disease
Coxsackie A

oral ulcers, maculopapular vesicular rash on hands and feet, sometimes on buttocks
duodenal atresia
completel or partial failure of the duodenal lumen to recanalize during gestational weeks 8-10

polyhydramnios in utero; bilious emesis within hours after first feeding; a/w Down syndrome and other cardiac/GI abnormalities (like annular pancreas, malrotation and imperforate anus)

double bubble sign

surgery to repair
AML can present with a chloroma
-- greenish soft-tissue tumor of the skin or spinal cord
neuroblastoma
embryonal tumor of neural crest origin

<1year old...70% have distant mets at presentation

a/w neurofibromatosis, Hirschsprung's and N-myc oncogene

NONTENDER abd mass (may cross midline), horners syndrome, HTN or cord compression (from paraspinal tumor)

elevated 24 hr urinary catecholamines (VMA and HVA)
Wilms tumor
renal tumor of embryonal origin, 2-5 years old

a/w Beckwith Wiedemann syndrome (hemihypertrophy, macroglossia, visceromegaly), neurofibromatosis and WAGR (wilms, aniridia, GU and MR)

ASYMPTOMATIC, NONTENDER, smooth abd mass

abd pain, fever, HTN and microscopic/gross hematuria are seen
Ewing's sarcoma
neuroectodermal origin...from bone

mostly in Caucasian male adolescents

a/w chrom 11:22 translocation

local pain and swelling

commonly target midshaft of long bones - femur, pelvis, fibula and humerus (descen order)

systemic stuff: fever, anorexia, fatigue

LYTIC BONE LESION (ONION SKIN IF TUMOR PENETRATES THROUGH CORTEX)
"sunburst" lytic bone lesions
osteosarcoma - from osteoblasts of mesenchymal origin

male adolescents

systemic symptoms are RARE (as compared with Ewings)

METAPHYSES OF LONG BONES (ewings is midshaft)...distal femur, proximal tibia and proximal humerus...mets to lungs in 20% pts

increased LDH is worse prognosis

increaed alk phosp
most common type of tracheoesophageal fistula
esophageal atresia with distal TEF (85%)...cannot pass NG tube
not contraindications to vaccines
mild illness and/or low grade fever, current antibiotic therapy and prematurity
neonate has meconium ileus
CF or Hirschsprung's
bilious emesis within hours after first feeding
duodenal atresia
infant has high fever and onset of rash as fever breaks...babys at risk for what?
febrile seizures (roseola infantum)
chronic resp infections, nitroblue tetrazolium test is positive
chronic granulomatous disease
child has eczema, thrombocytopenia and high levels of IgA
Wiskott-Aldrich syndrome
4 month old infant has life-threatening Pseudomonas infection
bruton's x-linked agammaglobulinemia
sudden onsent of mental status changes, emesis and liver dysfunction after taking aspirin
Reye's syndrome
child has loss of red light reflex...
suspect retinoblastoma
vaccines at 6 month visit
HBV, DTaP, IPV, PCV
cause of neonatal RDS
surfactant deficiency
red "currant jelly" stools
intussusception
congenital heart disease that causes secondary HTN
coarctation of the aorta
first line tx for otitis media
amoxicillin x 10 days
most common pathogen causing croup
parainfluenza virus 1
homeless child small for his age, peeling skin and swollen belly
Kwashiorkor
defect in x-linked syndrome with MR, gout, self mutilation and choreoathetosis
Lesch-Nyhan syndrome (purine salvage problem with HGPRTase deficiency)
machinery murmur in newbord
PDA
farmer's lung
spores of actinomycetes from moldy hay
bird fancier's lung
antigens from feathers, excreta, serum
mushroom worker's lung
spores of actinomycetes from compost
malt worker's lung
spores of Aspergillus clavatus in grain
Grain handler's lung
grain weevil dust
Bagassosis
spores of actinomycetes from sugarcane
Air condition lung
spores of actinomycetes from air conditioners
Asbestosis
work involving SHIPBUILDING, tile or brake linings, insulation, construction...presents 15-20yrs after initial exposure

CXR: linear opacities of lung bases and interstitial fibrosis, CALCIFIED PLEURAL PLAQUES indicative of benign pleural disease

comp: increased risk of mesothelioma (rare) and lung cancer; risk of lung cancer is higher in smokers
Coal mine disease
CXR: small nodular opacities (<1cm) in upper lung zones; restrictive lung disease

progressive massive fibrosis
Silicosis
works in mines or quarries with glass, pottery or silica

CXR: small (<1cm) nodular opacities in upper lung zones; EGGSHELL CALCIFICATIONS

restrictive lung disease

increased risk of TB, annual skin test

progressive massive fibrosis
Berylliosis
work in high-tech fields such as aerospace, nuclear and electronic plants; ceramic industries; foundries; plating facilities; dental material sites, dye manufacturing

CXR: diffuse infiltrates, hilar adenopathy

requires chronic steroid treatments
usual interstitial pneumonia
most common form of interstital pneumonia
causes of obstructive pulmonary disease
asthma, bronchiectasis, cystic fibrosis and tracheal or bronchial obstruction
asthma
REVERSIBLE airway obstruction 2/2 bronchial hyperreactivity, airway inflammation, mucous plugging and SM hypertrophy

peak flow is diminished; FEV/FVC is decreased, residual volume and TLC increased

CXR: hyperinflation

methacholine challenge: test for bronchial hyperresponsiveness; useful when PFTs are normal
Isoproterenol
nonspecific beta agonist

relaxes bronchial SM (beta 2); tachycardia (beta 1) is an adverse effect
beta 2 agonists
albuterol: relaxes bronchial SM, used in acute attacks

Salmeterol: long acting agent for prophylaxis
methylxanthines
Theophylline

likely causes bronchodilation by inhibiting phosphodiesterase, thereby decreasing cAMP hydrolysis

usage is limited due to narrow therapeutic index (cardiotoxicity and neurotoxicity)
Ipratropium
muscarinic antagonists

competitive block of muscarinic receptors, prevents bronchoconstriction
Cromolyn
prevents release of mediators from mast cells; useful for exercise-induced bronchospasm, effective only in prophylaxis of asthma; not effective during an acute asthmatic attach...toxicity is rare
Beclomethasone
corticosteroid used in asthma

inhibits synthesis of virtually all cytokines; inactivate NF-kB, transcription factor that induces production of TNF-alpha, among other inflammatory agents

inhaled corticosteroids are first line tx for long term control of asthma
Zileuton

Zafirlukast
antileukotrienes

zileuton: 5-lipoxygenase pathway inhibitor; blocks conversion of arachidonic acid to leukotrienes

zafirlukast: blocks leukotriene receptors
Bronchiectasis
DILATION OF BRONCHI, permanent fibrosis, remodeling...caused by cycles of infection and inflammation of bronchi/bronchioles...

hx: cough with frequent bouts of yellow or green sputum production...a/w hx of pulm infections (pseudo, h flu and TB), and lots of other stuff...

CXR: TRAM LINES (parallel lines outlining dilated bronchi as a result of peribronchial inflammation and fibrosis), increased bronchovascular markings and HONEYCOMBING

high res CT: DILATED AIRWAYS...and ballooned cysts at end of bronchus
Chronic bronchitis
productive cough for > 3 months per year for 2 consecutive years

BLUE BLOATER - PRODUCTIVE COUGH, cyanosis with mild dyspnea; pts often overweight with peripheral edema...barrel chest, use of acc chest muscles, JVD, end-exp WHEEZING or muffled breath sounds
Emphysema
terminal airway destruction and dilation that may be due to SMOKING (centrilobular) or to alpha-1-antitrypsin deficiency (panlobular)

PINK PUFFER - dyspnea, pursed lips, thin wasted appearance

parenchymal bullae or subpleural blebs
an increased A-a gradient indicates...
V/Q mismatch or a diffusion impairment.

(random...in hypercapnic pts, increase minute ventilation...if give more O2, may suppress hypoxic resp drive)
ARDS
ACUTE ONSET, ratio PaO2/FiO2 < 200, diffuse infiltration, swan ganz wedge pressure < 18mmHg (non-cardiogenic pulm edema)

2/2 endothelial injury, common causes are sepsis, pneumonia, aspiration, multiple blood transfusions, inhaled/ingested toxins and trauma...overall mortality is 30-40%

minimize injury induced by mechanical ventilation by ventilating with low tidal volumes...use PEEP to recruit collapsed alveoli and titrate PEEP and FiO2 to achieve adequate oxygenation
pulmonary HTN
mean pulmonary art pressure > 25mmHg (nl 15mmHg)

causes: left sided heart failure, mitral valve disease, congenital heart disease with L to R shunt, hypoxic vasoconstriction (2/2 chronic lung disease), increased resistance in pulm veins, thromboembolic disease...remodeling 2/2 structural lung disease

loud, palpable S2 (often split)...systolic ejection murmur, S4 or parasternal heave
CXR for PE
may show atelectasis, pleural effusion...HAMPTONS HUMP: wedge shaped infarct, WESTERMARKS SIGN: oligemia in embolized lung zone
EKG in PE
not diagnostic, sinus tach

classic triad of S1Q3T3 - acute right heart strain with an S wave in lead I, a Q wave in lead III and inverted T in III - uncommon!
lung nodules...char favoring malignancy
age > 45-50; smoking history, history of malignancy, new or larger lesions, absence of calcifications or irregular calcifications, > 2cm, irregular margins
Characteristics favoring benign lung nodule
age < 35, no change from old films, central/uniform/laminated/popcorn calcifications, size < 2cm, smooth margins
lung cancer NOT associated with smoking
bronchoalveolar carcinoma

(an adenocarcinoma)
small cell lung cancer
highly correlated with cigarette exposure

central location

neuroendocrine origin; a/w paraneoplastic syndromes

commonly presents with mets (intrathoracic and extrathoracic sites such as brain, liver and bone)

paraneoplastic processes a/w small cell lung cancer: Cushing's (ACTH), SIADH leading to hyponatremia, peripheral neuropathy, subacute cerebellar degeneration, myasthenia (eaton-lambert syndrome)
non small cell lung cancer
less propensity to metastasize

paraneoplastic: hypertrophic pulmonary osteoarthropathy, digital clubbing
adenocarinoma of the lung
MOST COMMON TYPE OF LUNG CANCER

PERIPHERAL location

includes bronchoalveolar carcinoma which is a/w multiple nodules, interstitial infiltration and prolifer sputum production

paraneo: thrombophlebitis, nonbacterial verrucous endocarditis, hypercoagulability
squamous cell carcinoma of the lung
central location; 98% are in smokers

paraneoplastic: HYPERCALCEMIA (PTHrP)
large cell/neuroendocrine carcinomas of the lung
least common; a/w poor prognosis

a/w gynecomastia
lung cancer can present with...
Horner's: miosis, ptosis and anhidrosis in patients with Pancoast's tumor at apex of the lung

superior vena cava syndrome: obstruction of SVC with supraclavicular venous engorgement

Hoarseness: due to recurrent laryngeal nerve involvement

Paraneoplastic syndromes
tx of small cell lung cancer
unresectable

chemotherapy is mainstay of tx.

usually metastasized at time of diagnosis
tx of non-small cell lung cancer
surgical resection in early stages (IA, IB, IIA, IIB and poss IIIA)

supplement surgery with radiation and chemo

palliation for symptomatic but unresectable disease
causes of transudate pleural effusion
CHF, cirrhosis or nephrotic syndrome

(increased pulm cap wedge pressure, dec oncotic pressure)
exudative pleural effusion
causes: pneumonia (parapneumonic effusion), TB, malignancy, pulmonary embolism, collagen vascular disease (RA, SLE), pancreatitis, trauma

2/2 increased pleural vascular permeability

ratio of pleural to serum protein is >0.5

ratio of pleural to serum LDH is >0.6

pleural fluid LDH is more than 2/3 of upper normal limit of serum LDH
parapneumonic effusion
complicated in setting of + gram stain or culture OR pH < 7.2 OR a glucose level of <60

presence of PUS indicates an EMPYEMA
primary spontaneous pneumothorax
due to rupture of subpleural apical blebs

usually found in tall, thin young males
secondary pneumothorax
due to COPD, TB, trauma, PCP and iatrogenic factors (thoracentesis, subclavian line placement, positive pressure mechanical ventilation, bronchoscopy)
tension pneumo
pulmonary or chest wall defect that acts as a one-way valve, drawing air into the pleural space including penetrating trauma, infection and positive pressure mechanical ventilation

immediate needle decompression (2nd intercostal space at midclavicular line), then chest tube

presents with respiratory distress, falling O2 sats, hypotension, distended neck veins and tracheal deviation
normalizing PCO2 in patient with asthma exacerbation
fatigue and impending respiratory failure
dyspnea, lateral hilar lymphodenopathy on CXR, noncaseating granulomas, increased ACE and hypercalcemia
sarcoidosis
honeycomb pattern on CXR
diffuse interstitial pulmonary fibrosis; supportive care, steroids may help
treatment for SVC syndrome
radiation
tall white male presents with acute shortness of breath
spontaneous pneumothorax, spontaneous regression, supplemental O2 may be helpful
hypoxemia and pulmonary edema with normal pulmonary cap wedge pressure
ARDS
increased risk of what infection with silicosis?
TB
classic CXR findings for pulmonary edema
cardiomegaly, prominent pulmonary vessels, Kerley B lines, 'bats-wing' appearance of hilar shadows and perivascular and peribronchial cuffing
causes of hyperkalemia
1. spurious: hemolysis of blood samples, fist clenching in blood draws, rhabdo

2. decreased excretion - renal insufficiciency, drugs (spironolactone, triamterene, ACEIs, trimethoprin, NSAIDs, mineralocorticoid def/type IV RTA)

3. cellular shifts: tissue injury, insulin deficiency, acidosis, drugs (succinylcholine, digitalis, arginine, beta blockers)
hx of hyperkalemia
N/V, intesintal colic, areflexia, weakness, flaccid paralysis and paresthesias
EKG: peaked T waves, PR prolongation, wide QRS and loss of P waves

can progress to sine waves, ventricular fibrillation and cardiac arrest
HYPERKALEMIA, biotch.
tx of hyperkalemia
C BIG K

calcium gluconate!!! (for cardiac cell membrane stabilization)

bicarbonate and/or insulin + glucose to temporarily shift potassium into cells

kayexalate and loop diuretics to remove potassium from the body

beta agonists - promotes cellular reuptake of potassium
causes of hypokalemia
1. transcellular shifts - insulin, beta 2 agonists, alkalosis, familial hypokalemic periodic paralysis

2. GI losses - diarrhea, chronic laxative abuse, vomiting, NG suction

3. renal losses - diuretics (loop or thiazide), primary mineralocorticoid excess or secondary hyperaldosteronism, decreased circulating volume, Bartter's syndrome, drugs (eg gentamycin, amphotericin), DKA, hypomagnesemia, type I RTA (defective distal H+ secretion)

consider RTA in setting of metabolic acidosis
hx of hypokalemia
muscle weakness, cramps, fatigue, hyporeflexia, paresthesias, rhabdomyolysis and ascending paralysis
EKG- T wave flattening, U wave (additional wave after the T wave) and ST segment depression can lead to AV block and subsequent cardiac arrest
hypokalemia
tx of hypokalemia
replete K and also magnesium - as hypomagnesia complicates potassium repletion
cause of hypercalcemia
calcium supplementation, hyperparathyroidism, iatrogenic (thiazides), immobility, milk-alkali syndrome, paget's disease, addisons disease/acromegaly, neoplasm, zollinger-ellison syndrome (MEN 1), excess vitamin A, excess vitamin D, sarcoidosis

(can see short QT with hypercalcemia)
abd muscle cramps, dyspnea, tetany, perioral and acral paresthesias and convulsions
hypocalcemia

Chvostek's sign - tapping of facial nerve

Trousseau's sign - carpal spasm after arterial occlusion of BP cuff

may show PROLONGED QT INTERVAL...
causes of increased anion gap
methanol.

uremia.

DKA.

Paraldehyde.

Intoxication.

Lactic acidosis.

Ethylene glycol.

Salicylates.

if normal anion gap: diarrhea, glue sniffing, RTA or hyperchloremia
early aspirin ingestion can cause...
respiratory alkalosis
causes of metabolic alkalosis with compensation
vomiting, diuretic use, antacid use or hyperaldosteronism
renal tubular acidosis
net decrease in either tubular H+ secretion or HCO3- reabsorption that leads to a NON-ANION GAP METABOLIC ACIDOSIS

three main types of RTA, type IV (distal) is the MOST COMMON FORM!!!
type I RTA
distal - defect in H+ secretion

etiologies: hereditary, amphotericin, cirrhosis, autoimmune disorders, sickle cell disease and lithium

Tx: potassium citrate

complications: nephrolithiasis
type II (proximal) RTA
defect in HCO3- resorption

etiologies: hereditary, carbonic anhydrase inhibitors, Fanconi's syndrome, MM

Tx: potassium citrate

Complications: rickets, osteomalacia
Type IV (distal) RTA
defect is aldosterone deficiency or resistance leads to defects in sodium reabsorption and H+/K+ excretion

etiologies: hyporeninemic hypoaldosteronism; chronic kidney disease from DM, HTN and HIV

tx: furosemide, fludrocortisone, and low potassium diet in pts with aldosterone def

complications: hyperkalemia
acute interstitial nephritis
fever, arthralgias, and a pruritic, erythematous rash...methicillin is the classic association
FeNa < 1%, Urine sodium < 20, urine specific gravity > 1.020 or a BUN/Creatinine ratio > 20 suggest...
pre-renal etiology of acute renal failure
indications for urgent dialysis
acidosis

electrolyte abnormalities (hyperkalemia)

ingestions - salicylates, theophylline, methanol, barbiturates, lithium, ethylene glycol

overload - fluid

uremic symptoms - pericarditis, encephalopathy, bleeding, nausea, pruritis and myoclonus
hyaline casts (urine sediment)
normal finding, but increased amount suggests volume depletion

prerenal
red cell casts, dysmorphic red cells
glomerulonephritis

intrinsic renal disease
white cells, eosinophils

(urine sediment)
allergic interstitial nephritis, atheroembolic disease

intrinsic
granular casts, renal tubular cells, "muddy-brown cast"
ATN

intrinsic
white cells, white cell casts
pyelonephritis

postrenal etiology
carbonic anhydrase inhibitor
acetazolamide

acts on proximal convuluted tubule

mech: inhibits carbonic anhydrase, increases H+ reabsorption, blocks Na/H exchange

side effects: hyperchloremic metabolic acidosis, sulfa allergy
osmotic agents

(ie. mannitol, urea)
acts on entire tubule

increases tubular fluid osmolarity

side effects: pulmonary edema 2/2 CHF and anuria
Loop agents

(furosemide, ethacrynic acid, bumetanide, torsemide)
acts on ascending loop of henle

inhibits Na/K/Cl transporter

side effects: water loss, metabolic alkalosis, decreases potassium, decreases calcium, OTOTOXICITY, sulfa allergy (not ethacrynic acid - hyperuricemia)
thiazide agents

(HCTZ, chlorothiazide)
acts on distal convoluted tubule

inhibits Na/Cl transporter

side effects: water loss, metabolic alkalosis, decreases sodium, decreases potassium, increases glucose, increases CALCIUM, increases uric acid, sulfa allergy, pancreatitis
K sparing agents
spironolactone, triamterene, amiloride

acts on cortical collecting tubule

mech: aldosterone receptor antagonist (spironolactone)
blocks sodium channels (triamterene, amiloride)

side effects: metabolic acidosis, increases potassium, antiandrogenic effects - including gynecomastia (spironolactone)
nephritic syndrome in general
d/o of glomerular inflammation, aka glomerulonephritis

classic findings: oliguria, macroscopic/microscopic hematuria (smoky-brown urine), HTN and EDEMA!!! (may have small amt of proteinuria)

pts have decreased GFR with elevated BUN and creatinine; measure complement, ANA, ANCA and anti-GBM antibody levels...

tx: HTN, fluid overload and uremia; corticosteroids are useful in reducing glomerular inflammation in some cases
nephrotic syndrome in general
PROTEINURIA (> 3.5 g/day), generalized EDEMA, HYPOALBUMINEMIA and HYPERLIPIDEMIA

about 1/3 cases from systemic diseases like DM, SLE or amyloidosis

hx: generalized edema, FOAMY URINE, increased susceptibility to infection and predisposition to hypercoagulable states...increased risk of venous thrombosis and pulmonary embolism

tx: protein and salt restriction, ACE inhibitors decrease proteinuria and diminish progression...

vaccinate with 23-polyvalent pneumococcus vaccine (PPV23) - patients at increased risk of Strep pneumo
list of causes of nephritic syndrome
Immune complex - postinfectious glomerulonephritis, IgA nephropathy (Berger's dz)

Pauci immune - Wegener's granulomatosis

Anti-GBM disease - Goodpasture's syndrome and Alport's syndrome
list of causes of nephrotic syndrome
minimal change, focal segmental glomerular sclerosis, membranous nephropathy, diabetic nephropathy, lupus nephritis, renal amyloidosis, membranoproliferative nephropathy
post infectious glomerulonephritis
NEPHRITIC

a/w recent group A beta hemolytic streptococcal infection (within 2 weeks)

hx: oliguria, edema, HTN, smoky brown urine

LOW SERUM C3!!!!, increased ASO titer, lumpy-bumpy immunofluorescence
IgA nephropathy (Berger's disease)
MOST COMMON TYPE
NEPHRITIC

a/w upper resp or GI infections, commonly seen in young men; may be seen in HSP

episodic gross hematuria or persistent microscopic hematuria

NORMAL C3

tx: glucocorticoids for select pts, ACEIs in pts with proteinuria

20% progress to ESRD
Wegener's granulomatosis
NEPHRITIC (pauci-immune)

granulomatous inflammation of the respiratory tract and kidney with necrotizing vasculitis

hx: fever, weight loss, hematuria, hearing disturbances, resp and sinus symptoms, cavitary pulmonary lesions bleed and lead to HEMOPTYSIS

C-ANCA!!! (cell mediated immune response)...renal biopsy shows segmental necrotizing glomerulonephritis with few immunoglobulin deposits on immuno-fluorescence

tx: high dose corticosteroids and cytotoxic agents; pts have frequent relapses
Goodpasture's
Nephritic

Anti-GBM disease

glomerulonephritis with pulmonary hemorrhage; peak incidence in men in their mid-20s

HEMOPTYSIS, dyspnea, possible resp failure

LINEAR ANTI-GBM DEPOSITS on immunofluorescence; iron def anemia; hemosiderin-filled macrophages in sputum; pulm infiltrates on CXR

tx: plasma exchange tx, pulsed steroids, may progress to ESRD
Alport's syndrome
nephritic

hereditary glomerulonephritis; presents in boys 5-20 yrs of age

asymptomatic hematuria a/w NERVE DEAFNESS and eye disorders

GBM splitting on EM

tx: progresses to renal failure; anti-GBM nephritis may recur s/p transplant
minimal change disease
most common nephrotic syn in children, idiopathic, 2' causes include NSAIDs and hematologic malignancies

tendency towards infections and thrombotic events

light mic is NORMAL

EM: FUSION of EPITHELIAL FOOT PROCESSES with lipid laden renal cortices

tx: steroids - excellent prognosis
focal segmental glomerular sclerosis
nephritic

idiopathic, IV drug use, HIV infection, obesity

typical pt is young black male with uncontrolled HTN

microscopic hematuria; biopsy - sclerosis in capillary tufts

tx: prednisone, cytotoxic tx
most common nephropathy in caucasian adults
MEMBRANOUS NEPHROPATHY

2' causes includes solid tumor malignancies (esp in pts > 60 yrs old) and immune complex disease

a/w HBV, syphilis, malaria and gold

SPIKE AND DOME 2/2 granular deposits of IgG and C3 at BM

tx: prednisone and cytotoxic therapy for severe disease
Kimmelstiel-Wilson lesions

increased mesangial matrix
diabetic nephropathy

two forms: diffuse hyalinization and nodular glomerulosclerosis

long standing, poorly controlled DM with evidence of retionpathy or neuropathy

tx: tight control of blood sugars; ACEIs for type I and ARBs for type 2
Lupus nephritis
WHO types I-IV

both nephrotic and nephritic

severity of renal disease often determines overall prognosis...

proteinuria or RBCs on UA ma be found during evaluation of SLE patients

mesangial proliferation, subendothelial immune complex deposition

tx: prednisone and cytotoxic therapy may decrease disease progression
Renal amyloidosis
primary (plasma cell dyscrasias) and secondary (infectious or inflammatory) are most common

pts with MM or chronic inflam dz (RA, TB)

CONGO RED STAIN; APPLE GREEN birefringence under polarized light

tx: prednisone and melphalan; bone marrow transplant may be used for MM
membranoproliferative nephropathy
a/w HCV, dammit!!! cryoglobulinemia, lupus and subacute bacterial endocarditis

slow progression to renal failure

TRAM TRACK, double layered BM; type I has subendothelial deposits and mesangial deposits; all three types have low serum C3

tx: corticosteroids and cytotoxic agents may help
calcium oxalate/calcium phosphate stones
most common stones (most common are calcium oxalate)

etiology: idiopathic hypercalciuria, elevated urine acid 2/2 to diet and 1' hyperparathyroidism, alkaline urine

radiopaque!

tx: hydration and thiazide diuretic
Struvite stones
9%

triple phosphate stones

a/w urease-producing organisms (Proteus, Klebsiella), form staghorn calculi, alkaline urine, radiopaque, increased ammonia

tx: hydration, tx UTI if present
Uric acid stones
7%

a/w gout and high purine turnover states

acidic urine (pH < 5.5)

RADIOLUCENT (cannot see on x-ray)

tx: hydration, alkalinize urine with citrate, which is converted to HCO3 in the liver; dietary purine restriction and allopurinol
Cystine stones
least common

hexagonal crystals

2/2 defect in renal transport of certain amino acids (COLA - cystine, ornithine, lysine and arginine)

HEXAGONAL CRYSTALS

radiopaque

tx: hydration, alkalinize urine, penicillamine
AR PCKD
less common but more severe

infants and young children with renal failure, liver fibrosis and portal hypertension; may lead to death in first few years of life
AD PCKD
most common

starts to be sympt > 30 yrs old

a/w increased risk of cerebral aneurysm, especially in pts with + fm history

extrarenal complications: hepatic cysts, valvular heart disease, colonic diverticula, abd wall and ing hernia

hx: PAIN AND HEMATURIA, other findings - HTN, hepatic cysts, cerebral berry aneurysms, diverticulosis and mitral valve prolapse
cryptorchidism
failure of testes to descend into scrotum

prematurity is a huge risk factor

bilateral cryptorchidism is a/w oligospermia and infertility

tx: orchiopexy after age one (in all but 1% of males, testes will descend by that age) but before age 5 (to preserve fertility)

if discovered later, tx with orchiectomy to avoid risk of testicular cancer
risk factors for erectile dysfunction
DM, atherosclerosis, meds (beta-blockers, SSRIs), HTN, heart disease, surgery or radiation for prostate cancer and spinal cord injury
tx of erectile dysfunction
Sildenafil (Viagra), Vardenafil (Levitra) and Tadalafil (Cialis)

phosphodiesterase-5 inhibitors that prolong action of cGMP-mediated SM relaxation and increase blood flow in the corpora cavernosa...effective but contraindicated in pts taking nitroglycerin

testosterone is useful for pts with hypogonadism of testicular or pituitary origin; discouraged for pts with normal testosterone levels
tx of BPH
medical therapy with alpha-blockers (terazosin) and 5-alpha-reductase inhibitors (finasteride) to reduce mild to moderate symptoms

TURP (transurethral resection of the prostate) or open prostatectomy for pts with moderate to severe symptoms
major side effect of alpha blockers (for BPH)
orthostatic hypotension
leading causes of cancer death in men
1. lung cancer
2. prostate cancer
3. colorectal cancer
4. pancreatic cancer
5. leukemia
tx of metastatic prostate cancer
androgen ablation (eg. GnRH agonists, orchiectomy, flutamide) and chemotherapy
differential for hematuria
strictures, stones, infection, inflammation, infarction, tumor, trauma and TB
lets talk about bladder cancer
most frequent malignant tumor of urinary tract

transitional cell carcinoma

risk factors: smoking, diets rich in meat and fat, schistosomiasis, chronic tx with cyclophosphamide and exposure to aniline dyes (benzene derivative)

hx: GROSS HEMATURIA - most common presenting symptom

dx: CYSTOSCOPY WITH BX IS DIAGNOSTIC..IVP

tx: depends on extent of spread beyond the bladder mucosa...

superficial cancers: complete transurethral resection or intravesicular chemo with mitomycin C or BCG (TB vaccine)
renal cell carinoma...whhhatt.
adenocarcinoma from tubular epithelial cells

tumors can spread along renal vein to the IVC and can metastasize to lung and bone

risk factors: male gender, smoking, obesity, acquired cystic kidney disease in ESRD and von Hippel-Lindau disease
classic triad of RCC
hematuria, flank pain and palpable flank mass

many have fever...varicocele is common

ANEMIA IS COMMON AT PRESENTATION, BUT POLYCYTHEMIA 2/2 increased EPO production may be seen in 5-10% pts
testicular cancer shiznit.
95% derive from germ cells and virtually all are malignant

cryptorchidism a/w increased risk of neoplasm in both testes

Klinefelter's also risk factor

most common malignancy in men 25-34

hx: painless enlargement of testes

seminomas peak b/t 40-50yo
beta-hCG in test. cancer
always elevated in choriocarcinoma and elevated in 10% seminomas
alpha-fetoprotein in test. cancer
often elevated in nonseminomatous germ cell tumors, particularly endodermal sinus (yolk sac) tumors
testicular seminomas
exquisitely radiosensitive and also respond to chemotherapy

(platinum based chemo for nonseminomatous germ cell tumors)
renal tubular acidosis a/w abnormal H+ secretion and nephrolithiasis
Type I (distal) RTA
RTA a/w abnormal HCO3 and rickets
Type II (proximal) RTA
RTA a/w aldosterone defect
Type IV (distal) RTA
"doughy skin"
hypernatremia
differential of hypervolemic hyponatremia
cirrhosis, CHF, nephritic syndrome
most common causes of hypercalcemia
malignancy and hyperparathyroidism
hematuria, hypertension and oliguria
nephritic syndrome
proteinuria, hypoalbuminemia, hyperlipidemia, hyperlipiduria and edema
nephrotic syndrome
presence of red cell casts in urine sediment
glomerulonephritis/nephritic syndrome
waxy casts in urine sediment and Maltese crosses (seen with lipiduria)
nephrotic syndrome
drowsiness, asterixis, nausea and pericardial friction rub
uremic syndrome seen in pts with renal failure
low urine specific gravity in presence of high serum osmolality
DI
testicular cancer a/w beta-hCG and alpha fetoprotein
choriocarcinoma
salicylate ingestion - what type of acid-base d/o?
anion gap acidosis and primary respiratory alkalosis due to central respiratory stimulation
acid-base disturbance commonly seen in pregnant women
respiratory alkalosis
three systemic diseases that lead to nephrotic syndrome
DM, SLE and amyloidosis
elevated EPO, elevated Hct and normal O2 sats suggest?
RCC or other EPO-producing tumor; evaluate with CT scan
L4 nerve root
motor: foot dorsiflexion (tibialis anterior)

reflex: patellar

sensory: medial aspect of lower leg
L5 nerve root
motor: big toe dorsiflexion (extensor hallucis longus), foot eversion (peroneu muscles)

no reflex a/w L5

sensory: dorsum of the foot and lateral aspect of the lower leg
S1 nerve root
Motor: plantar flexion (gastrocnemius/soleus), gluteus maximus (hip extension)

Reflex: achilles

Sensory: plantar and lateral aspects of the foot
most common spot for Herniated Disk
L4-L5 and L5-S1
cauda equina syndrome
bowel or bladder dysfunction (urinary overflow incontinence), impotence and saddle-area anesthesia

surgical emergency!!
spinal stenosis
usually 2/2 degenerative joint disease

leg cramping worse at rest, with standing and with walking (pseudo or neurogenic claudication)

symptoms improve with flexion at the hips and bending forward

if refractory to med tx, may do surgical laminectomy - achieves significant short term success, but many have recurrence of symptoms
anterior dislocation of the shoulder
most common

AXILLARY ARTERY AND NERVE are at risk

patients hold arm in external rotation

tx: reduction followed by sling and swath; recurrent dislocations may need surgical repair
posterior dislocation of the shoulder
a/w seizure and electrocusions

can injure RADIAL ARTERY

pts hold arm in internal rotation
posterior hip dislocation
MOST COMMON!! (>90%)

occurs via posteriorly directed force on an internally rotated, flexed, adducted hip (dashboard injury)

a/w risk of sciatic nerve injury and avascular necrosis

tx: closed reduction followed by abduction pillow/bracing...evaluate with CT scan after reduction
anterior hip dislocation
not that common

can injury obturator nerve
Colles' fracture
distal radius...fall on outstretched hand...dorsally displaced, dorsally angulated fracture

tx: closed reduction by application of long-arm cast

open reduction if fracture is intra-articular
Scaphoid (carpal navicular) fracture
MOST COMMONLY FRACTURED CARPAL BONE

may take two weeks for radiographs to show fracture...

assume fracture if tenderness in ANATOMICAL SNUFF BOX

tx: thumb spica cast; if displacement or navicular nonunion present - tx with open reduction (if displacement)

with proximal 3rd scaphoid fractures, AVN may result from disruption of blood flow
boxer's fracture
5th metacarpal neck fracture

2/2 trauma of closed fist

tx: closed reduction with ulnar gutter splint; percutaneous pinning if fracture is excessively angulated

if skin is broken - assume infection by human oral pathogens...surgical irrigation, debridement and IV antibiotics (covering Eikenella)
Humerus fracture
RADIAL NERVE PALSY - wrist drop and loss of thumb abduction

tx: hanging arm cast vs. coaptation splint and sling

functional bracing
Nightstick fracture
ulnar shaft fracture resulting from self defense

tx: open reduction and internal fixation (ORIF) if significanly displaced
Monteggia's fracture
diaphyseal fracture of proximal ulna with subluxation or radial head

tx: ORIF of the shaft fracture (due to poor fracture diaphyseal blood supply) and closed reduction of radial head
Galeazzi's fracture
diaphyseal fracture of radias with dislocation of distal radioulnar joint

from direct blow to radius

tx: ORIF of radius and casting of fracture forearm in supination to reduce distal radioulnar joint
hip fracture
increased risk with osteoporosis...presents with shortened and externally rotated leg

DISPLACED FEMORAL NECK FRACTURES: a/w increased risk of AVN, nonunion and DVTs

tx: ORIF with parallel pinning of femoral neck; displaced fractures in elderly pts ma require hip hemiarthroplasty

anticoagulate to decrease likelihood of DVTs
femoral fracture
direct trauma...beware of fat emboli - fever, change in mental status, dyspnea, hypoxia, petechiae and decreased platelets

tx: intramedullary nailing of the femur; irrigate and debride open fractures
achilles tendon rupture
sudden "pop" like a rifle shot; more likely with decreased physical deconditioning

exam: limited plantar flexion and a + Thompson's test (pressure on the gastrocnemius leads to absent foot plantar flexion)

tx: surgically followed by long leg cast for 6 weeks
ACL injury
results from noncontact twisting mechanism, forced hyperextension or impact to an extended knee, + anterior drawer and Lachman tests; r/o meniscal or MCL injury

tx: generally surgical with graft from patellar or hamstring tendons
PCL injury
from forced hyperextension
+ posterior drawer test

tx: operative for highly competitive athletes
Meniscal tears
from acute twisting injury or degenerative tear in elderly pts

clicking or locking may be present

joint line tenderness and + McMurray's test

operative for younger pts with significant tears or older pts whose symptoms did not respond to conservative management
Nursemaid's elbow
radial head subluxation that typically occurs as a result of being pulled or lifted by the hand

presents with pain and refusal to bend the elbow

tx: manual reduction by gentle supination of the elbow at 90 degrees of flexion; no immobilization
Supracondylar humerus fracture
tends to occur at 5-8 yrs old

proximity to brachial artery increases risk of Volkmann's contracture (results from compartment syndrome of the forearm)

tx: cast immobilization; closed reduction with percutaneous pinning if significantly displaced
Osgood-Schlatter dz
overuse apophysitis of tibial tubercle, localized pain, especially with quadriceps contraction, in active young boys

tx: decrease activity for 2-3 months or until asymptomatic; neoprene brace may provide symptomatic relief
salter-harris fracture
fractures of growth plates in children

5 different types

types III-V: surgical repair to prevent complications such as leg length inequality
Developmental dysplasia of the hip
aka: congenital hip dislocation

can result in subluxed, dislocatable or dislocated femoral heads...can lead to early degenerative joint disease of the hips

dislocations result from poor development of the acetabulum and hip 2/2 lax musculature and EXCESSIVE UTERINE PACKING in the flexed and adducted position (eg. breech presentation) --> excessive stretching of the posterior hip capsule and adductor muscle contracture
History of developmental dysplasia of hips
FIRST BORN FEMALES in BREECH POSITION
Barlow's maneuver
DDH

pressure placed on inner aspect of abducted thigh and hip is then adducted - audible "clunk" as femoral head dislocates posteriorly
Ortolani's maneuver
thighs are gently abducted from midline with ant pressure on greater trochanter...SOFT CLICK signifies reduction of femoral head into acetabulum
other stuff with DHH (rando)
Allis (Galeazzi's) sign: knees are at unequal heights when hips and knees are flexed (dislocated side is lower)

Asymmetric skin folds and limited abduction of the affected hip
Tx of DDH
early detection is critical

u/s may be helpful, esp after 10 weeks of age

radiographs unreliable until pts > 4months because of radiolucency of neonatal femoral head

< 6months: splint with PAVLIK HARNESS (maintains hip flexed and abducted)...dont flex hips >60 degrees to prevent AVN

6-15months: spica cast

15-24 months: open reduction followed by spica cast

complications: joint contractures and AVN of femoral head

without tx, significant defect is likely in patients < 2 yrs of age
Legg-Calve Perthes Disease
idiopathic AVN of the femoral head

most commonly in boys 4-10yo

usually self-limited with symptoms lasting < 18 months

history/PE: asymptomatic at first, but pts can develop painless limp; if there is pain - groin or anterior thigh, or referred to the knee

LIMITED ABDUCTION AND INTERNAL ROTATION, atrophy of affected leg; usually unilateral - 85-90%

tx: OBSERVATION if limited femoral head involvement or full ROM

if extensive or decrease ROM - consider bracing, petrie cast or an osteotomy

prognosis good if pt < 5yo and has full ROM, decreased fem head involvement and stable joint
Slipped Capital Femoral Epiphysis (SCFE)
separation of proximal femoral epiphysis through growth plate --> medial and posterior displacement of femoral head (relative to femoral neck)

may be 2/2 imbalance btw growth hormone and sex hormones

risk factors: obesity, age, 11-13 yrs old, male gender and african american ethnicity

a/w hypothyroidism

hx: acute or insidious THIGH or KNEE PAIN and a PAINFUL LIMP

acute cases present with restricted ROM and commonly INABILITY TO BEAR WEIGHT

bilateral in 40-50% cases

limited internal rotation and abduction of hip...on flexion of hip, obligatory external rotation 2/2 physical displacement...further loss of internal rotation with hip flexion

Dx: BOTH hips in AP and FROG-LEG LATERAL VIEWS reveal POSTERIOR AND MEDIAL DISPLACEMENT of femoral heads

r/o hypothroidism with TSH

tx: no weight bearing; gentle closed reduction in acute slips

ext fixation - surgical pinning where it lays...lesseens risk of AVN and chondrolysis

complications: ANV of fem head, chondrolysis and premature hip osteoarthritis --> hip arthroplasty
Osteosarcoma
2nd most common primary malignant tumor of bone (1st is MM)

METAPHYSEAL areas of DISTAL FEMUR, PROXIMAL TIBIA and proximal humerus...often mets to lungs

some cases preceeded by Paget's; risk factors include male gender and age 20-30

presents as progressive and eventually intractable PAIN THAT IS WORSE AT NIGHT

dx: CODMANS TRIANGLE (periosteal new bone fmt at diaphyseal end of lesion)

SUNBURST PATTERN of osteosarcoma

(Ewing's has onion skinng)

tx: limb sparing surgical procedures and pre/post-op chemo (methotrexate, doxorubicin, cisplatin and ifosfamide), may need amputation
Colchicine
inhibits chemotaxis and is most effective when used early during a gout flare (use is limited by a narrow therapeutic window)
causes of hyperuricemia
increased cell turnover (hemolysis, blast crisis, tumor lysis, myelodysplasia, psoriasis)

cyclosporine, dehydration, diabetes insipidus, diet (increased red meat, alcohol), diuretics, lead poisoning, Lesch Nyhan syndrome, salicylates (low dose), starvation
Reactive arthritis
Reiter's syndrome

disease of young men, characteristic arthritis, uveitis, conjunctivitis and urethritis...

usuall follows infection with Campylobacter, Shigella, Salmonella, Chlamydia or Ureaplasma
ank spon
HLA B27

tx: NSAIDs (indomethacin) or for refractory cases - tumor necrosis factor inhibitors

may have anterior uveitis and heart block
dermatomyositis
may have heliotrope rash, "shawl sign" - rash involving shoulders, upper chest and back, Gottron's papules - papular rash with scales located on the dorsa of the hands, over bony prominences
Felty's syndrome
RA, splenomegaly and neutropenia
Rheumatoid Arthritis
chronic, destructive inflammatory arthritis with SYMMETRIC involvement of both large and small joints...causes synovial hypertrophy and pannus formation...leads to erosion of adjacent cartilage, bone and tendons...

risk factors: female, age 35-50 and HLA-DR4!!

hx: insidious onset of morning stiffness for > 1 hr with painful, warm swelling of multiple symmetric joints wrists, MCP and PIP joints)...

ulnar deviation

BAKERS CYSTS (palpable popliteal mass), vasculitis, atlantoaxial subluxation, carpal tunnel syndrome, rheumatoid nodules, keratoconjunctivitis sicca, pulm nodules, inflam endocarditis
tx of RA
NSAIDS - reduced or d/c'ed if tx successful with DMARDS (disease modifying antirheumatic drugs)

DMARDS should be started early...first line are hydroxychloroquine, sulfasalazine, methotrexate and azithioprine...2nd line include rituximab (anti-CD20) and leflunomide
anticentromere antibodies
CREST
anti-Scl 70 antibodies
a/w with poor prognosis of scleroderma
CREST
calcinosis, Raynaud's, esophageal dysmotility, sclerodactyly and telangiectasias

(diffuse form - pulmonary fibrosis)

can tx Raynaud's with calcium channel blockers

mortality 2/2 pulmonary hypertension and complications of pulmonary HTN
criteria for SLE
DOPAMINE RASH

discoid rash, oral ulcers, photosensitivity, arthritis, malar rash, immunologic criteria, neurologic symptoms (lupus cerebritis, seizures), elevated ESR, renal disease, + ANA, serositis, hematologic abnormalities
anti-ds DNA and anti-Sm antibodies
LUPUS
+ antihistone antibodies
drug induced SLE
neonatal SLE
+ anti-Ro antibodies
drugs that cause a lupus syndrome
chlorpromazine, hydralazine, INH, methyldopa, penicillamine, procainamide, quinidine
hip and back pain along with stiffness that improves with activity over the course of the day and worsens at rest
suspect ankylosing spondylitis

check HLA-B27
arthritis, conjunctivitis and urethritis in young men...dx?
associated organisms?
Reactive (reiter's) arthritis

a/w Campylobacter, Shigella, Salmonella, Chlamydia and Ureaplasma
active 13 year old boy with anterior knee pain...
Osgood Schlatter disease
complication of scaphoid fracture
avascular necrosis
signs of radial nerve damage
wrist drop, loss of thumb abduction
first born female who was born in breech position found to have asymmetric skin folds on her newborn exam...whats up?
developmental dysplasia of the hip

if severe, consider a Pavlik harness to maintain abduction
11 year old obese, African American boy presents with sudden onset of limp...dx, w/u?
slipped capital femoral epiphyses

AP and frog-leg lateral view
most common primary malignant tumor of bone
multiple myeloma
pemphigus
pemphigus vulgaris

intraepidermal blister that leads to widespread painful erosions

MUCOUS MEMBRANE

antibodies against desmoglein molecules responsible for keratinocyte adherence leading to loss of cellular attachment

MIDDLE AGED (40-60)

+ Nikolsky's sign

ACANTHOLYIS - intraepidermal split with free-floating keratinocytes in blister
Bullous pemphigoid
separation at epidermal BM

60-80 years old

antibodies against bullous pemphigoid antigen, superficially in BM zone

BLISTERS ARE STABLE - roof consists of nearly normal epidermis

IgG and C3 at dermal-epidermal junctions

autoantibodies against BM glycoproteins BP230 and BP 180

- Nikolsky's sign

mucous membranes NOT involved
HSV 1
oral labial lesions

primary: typically presents in infancy with widespread, severe herpetic gingivostomatitis with oral erosions
HSV 2
genital lesions

often presents in adults with bilateral, erosive vesicular lesions with edema and lymphadenopathy
verrucae (warts)
many different types of HPV

usually benign, some subtypes of HPV (especially 16 and 18) can lead to squamous malignancies

cauliflower like...grows downward

dx: acetowhitening...

tx: destruction of tissue by curettage, cryotherapy or acid keratolytics...

genital warts tx locally with podophyllin, trichloroacetic acid, imiquimod or 5-FU
Pityrosporum orbiculare
yeast that causes Tinea Versicolor

normal on skin...pathogenic type called Malassezia furfur

KOH preparation of scale that reveals "spaghetti and meatballs" pattern of hyphae and spores

tx: selenium sulfide daily for one week, followed by application once weekly for prophylaxis
pyrethrin
aka: RID

tx of head and pubic lice
Scabies
Sarcoptes scabiei - tiny arthropod mates on skin surface

female digs passage into stratum corneum and lays eggs...burrowing leads to pruritis...

hx: intense pruritis especially at night; hands, axillae and genitals...exam: mite's track can sometimes be seen along with erythematous, excoriated papules

Tx: 1-2 applications of PERMETHRIN

oral IVERMECTIN also effective...

pruritis may persist for two weeks after treatment...symptomatic tx should be used after this
Lichen planus
violaceous, flat-topped, polygonal papules

may have Wickham's striae (white stripes), especially on mucous membranes

Koebner's phenomenon - lesions that appear at the site of trauma...initially on genitalia

histology: "lichenoid pattern" - band of T lymphocytes at the epidermal-dermal junction with damage to the basal layer

tx: mild cases with corticosteroids

P disease: planar, purple, pruritic, persistent, polygonal, penile, perioral, puzzling and Koebner's phenomenon
"christmas tree pattern"
Pityriasis Rosea

acute dermatitis that is pink and scaly

etiology unknown, may be due to viral infection with human herpesvirus 7 (HHV7)

HERALD PATCH

"cigarette paper"

asymptomatic...heal without tx in 2-3 weeks...can use skin lubrication, topical antipruritics and systemic antihistamines
class of drugs that may cause syndrome of muscle rigidity, hyperthermia, autonomic instability and EPS
antipsychotics (neuroleptic malignant syndrome)
side effects of corticosteroids
acute mania, immunosuppression, thin skin, osteoporosis, easy bruising, myopathies
treatment for DTs
benzodiazepines
tx for acetaminophen OD
N-acetylcysteine
Tx for opiod overdose
Naloxone
Tx for benzo overdose
Flumazenil
Tx for neuroleptic malignant syndrome
Dantrolene or bromocriptine
Tx for malignant hypertension
nitroprusside
Tx of AF
rate control rhythm conversion and anticoagulation
Tx of SVT
if stable, rate control with carotid massage or other vagal stimulation...if unsuccessful, consider adenosine
causes of drug induced SLE
INH, penicillamine, hydralazine, procainamide, chlorpromazine, methyldopa and quinidine
blood in the urethral meatus or high-riding prostate
bladder rupture or urethral injury
test to rule out urethral injury
retrograde cystourethrogram
radiologic evidence of aortic rupture or dissection
widened mediastinum (>8cm), loss of aortic knob, pleural cap, tracheal deviation to the right, depression of left main stem bronchus
acceptable urine output in trauma pt
50cc/hr
acceptable urine output in stable patient
30cc/hr
cannon "a" waves
third degree heart block
signs of neurogenic shock
hypotension and bradycardia
signs of increased ICP
Cushings triad...

hypertension, bradycardia and abnormal respirations
decreased CO, decreased pulmonary capillary wedge pressure, increased peripheral vascular resistance
hypovolemic shock
increased CO, decreased PCWP, decreased PVR
septic or anaphylactic shock
tx of cardiogenic shock
identify cause; pressors (eg dopamine)
tx of anaphylactic shock
diphenhydramine or epinephrine 1:1000
supportive tx for ARDS
continuous positive airway pressure
signs of air embolism
pt with chest trauma who was previously stable suddenly dies
trauma series
AP chest, AP/lateral C-spine, AP pelvis
4 D's of posterior circulation strokes
Diplopia

Dizziness

Dysphagia

Dysarthria
MCA strokes
aphasia (dominant hemisphere), neglect (nondominant hemisphere), contralateral paresis and sensory loss in the FACE and ARM, gaze preference toward the side of the lesion, homonymous hemianopia
ACA stroke
contralateral paresis and sensory loss in the LEG, amnesia, personality changes, foot drop, gait dysfunction, cognitive changes
PCA stroke
homonymous hemianopia, memory deficits, dyslexia/alexia
Basilar artery stroke
coma, "locked in" syndrome, cranial nerve palsies, apnea, visual crap, drop attacks, dysphagia, dysarthria, vertigo, "crossed" weakness and sensory loss affecting the ipsilateral face and contralateral body
neuro deficients in polio and Werdnig Hoffman
LMN lesions only 2/2 destruction of anterior horns; flaccid paralysis
multiple sclerosis
demyelination

scanning speech, intention tremor and nystagmus
ALS
combined upper and lower motor neuron lesions with no sensory deficits
tabes dorsalis
tertiary syphilis

degeneration of dorsal roots and dorsal columns; impaired proprioception, locomotor ataxia
subarachnoid hemorrhages
2/2 trauma, berry aneurysms, AVM or trauma in circle of willis (often at the MCA)
hx of subarachnoid hemorrhage
acute onset, intensely painful "thunderclap" headache often followed by neck stiffness

may have had sentinel bleed days to weeks earlier marked by HA, neck stiffness and N/V 2/2 leaking aneurysm

LP if CT - to look for RBCs, xanthochromia (yellowish CSF due to breakdown of RBCs), increased protein from RBCs and increased ICP
tx of subarachnoid hemorrhage
prevent rebleeding, keep SBP <150

prevent vasospasm and associated neurologic deterioration by giving calcium channel blockers, IV fluids and pressors to maintain BP

give phenytoin for seizure prophylaxis

decrease ICP

(CN III palsy with pupil involvement is a/w Berry aneurysms)
subdural hematomas
typically follows head trauma leading to rupture of bridging veins and accumulation of blood btw dura and arachnoid membranes...common in elderly and alcoholics

hx: headache, changes in mental status, contralateral hemiparesis and ipsilateral pupillary dilation

CT: Crescent shaped, concave hyperdensity that does NOT cross suture midline

tx: surgical evacuation if symptomatic
epidural hematomas
usually 2/2 lateral skull fracture --> tear of middle meningeal artery

hx: immediate loss of consciousness leads to a lucid interval (minutes to hours) then to a coma with hemiparesis...ultimately a "blown pupil" (watch out for impending brain stem compression)...

CT: lens-shaped CONVEX hyperdensity limited by sutures
Tx of migraine headaches
abortive therapy: triptans - 1st line, metoclopramide; consider symptomatic tx for nausea

prophylactic: beta-blockers (propranolol), TCAs (amitriptyline), CCBs and valproic acid
tx of cluster HA
acute: high flow O2, ergots, sumatriptans, intranasal lidocaine, corticosteroids

prophylactic: ergots, CCBs, prednisone, lithium, valproic acid and topiramate
Lambert-Eaton Myasthenic Syndrome
small cell lung carcinoma risk factor (60%)

Dx: repetitive nerve stimulation shows incremental response, autoantibodies to presynaptic calcium channels and a chest CT indicative of lung neoplasm

Tx: tx small cell lung carcinoma; tumor resection may reverse symptoms; Guanidine hydrochloride is mainstay of tx; anticholinesterases may also improve symptoms
scanning speech, intranuclear ophthalmoplegia and nystagmus
MS
MS
can have optic neuritis (painful loss of vision)

Lhermittes sign may be present - sharp pain traveling up and down neck with flexion

MRI: multiple, asymmetric, periventricular white matter lesions (Dawsons fingers), esp in corpus callosum

increase IgG in CSF

tx: steroids, avonex/rebif (interferon alpha), betaseron (interferon alpha 1b) and copaxone (copolymer 1)

mitoxantrone...

alt tx: cyclophosphamide, IVIG and plasmapharesis

symptomatic therapy: baclofen for spasticity, cholinergics for urinary retention, anti-cholinergics for urinary incontinenct or amitriptyline for painful paresthesias

glatiramer acetate - suppresses T-cells against myelin
ropinirole or pramipexole
dopamine agonists

side effect of pramipexole: uncontrolled gambling
selegiline
MAO-B inhibitor...may be neuroprotective and may decrease need for levodopa
Dural tails
meningioma

from dura mater or arachnoid
Medulloblastoma
primitive neuroectodermal tumor

common in children

arises from 4th ventricle and increases ICP

HIGHLY MALIGNANT; may seed the subarachnoid space

posterior vermis sign - truncal dystaxia
Neurofibromatosis 1
AD, chromosome 17

aka: von Recklinghausen's syndrome

cafe au lait spots, freckling in axillary or inguinal area, optic glioma, two lisch nodules (pigmented iris hamartomas), bone abnormality, first degree relative with NF1

clinically evident by age 15
NF 2
AD, chromosome 22

BILATERAL ACOUSTIC NEUROMAS

first degree relative with NF2

unilateral acoustic neuromas

neurofibromas, meningiomas, gliomas or schwannomas

seizures, skin nodules, cafe au lait spots

clinically evident by age 20
tuberous sclerosis
AD

convulsive seizures, "ash leaf" hypopigmented lesions, MR

sebaceous adenomas (small red nodules on nose and cheeks in butterfly shapes)

shagreen patch (rough papule in lumbosacral region with an orange-peel consistency)

two retinal lesions: mulberry tumors and phakomas (round, flat, gray lesions)

lots of systems can be involved...CHF from rhabdomyoma...renal involvement may include hamartomas, angiomyolipomas or rarely, RCC

head CT: calcified tubers within cerebrum in the periventricular area

renal CT: angiomyolipomas (causing cystic or fibrous pulmonary changes)
Brocas
d/o of language production, including writing with intact comprehension

posterior inferior frontal gyrus is messed...often 2/2 left superior MCA stroke

impaired repetition, frustration, arm and face hemiparesis
Wernickes
d/o of language comprehension with intact yet nonsensical production

sensory aphasia

left posterior superior temporal (perisylvian) lobe...2/2 inferior/posterior MCA

preserved fluency, impaired repitition and comprehension..."word salad"...lack of awareness...

may have right upper homonymous quadrantanopia 2/2 involvement of Meyer's loop
Locked in syndrome
pts awake and alert but can move only eyes and eyelids

a/w central pontine myelinolysis, brain stem stroke and advanced ALS
persistent vegatative state
normal sleep-wake cycles but lack of awareness of self or the environment

most commonly caused by trauma with diffuse cortical injury or hypoxic ischmic injury
Wernicke's encephalopathy
encephalopathy, ophthalmoplegia (nystagmus, lateral rectus palsy, conjugate gaze palsy) and ataxia

pts: alcoholics, hyperemesis, starvation, renal dialysis and AIDS

can be elicited by high dose glucose administration
closed angle glaucoma
risk factors: PUPILLARY DILATION (prolonged time in darkened area, stress, meds), anterior uveitis and lens dislocation

hx: presents with EXTREME PAIN and blurred vision

HARD, RED EYE seen...pupil dilated and nonreactive to light

MEDICAL EMERGENCY that may lead to blindness...need to decrease intraocular pressure with acetazolamide and then pilocarpine...laser iridotomy
open angle glaucoma
risk factors: age > 40, african american ethnicity, diabetes and myopia

hx/PE: initially asymptomatic; frequent lens changes...defect in peripheral visual fields...CUPPING of optic disk

almost always bilateral

dx: tonometry, look at optic nerve...diseased trabecular meshwork that obstructs proper drainage of the eye...gradulal loss of vision...tunnel vision

tx: frequent optho exams...topical beta blockers - timolol, betaxolol to decrease aqueous humor production or with pilocarpine to increase aqueous outflow

can use carbonic anhydrase inhibitors...
Central retinal artery occlusion
sudden, painless unilateral blindness...cherry-red spot on the fovea, retinal swelling and retinal arteries that may appear bloodless

tx: THROMBOLYSIS within 8 hrs of symptom onset...decrease intraocular pressure through drainage of anterior chamber...may use IV acetazolamide to improve retinal perfusion...if no tx, may have retinal infarction and permanent blindess may result
Central retinal vein occlusion
subacute monocular visula loss..."blood and thunder", cotton wool spots...edema/optic disk swelling...dilated veins

tx: laser photocoagulation has variable results
most common primary sources of mets to the brain
lung, breast, skin (melanoma), kidney and GI tract
most common cause of seizures in children (2-10yo)
infection, febrile seizures, trauma and idiopathic
most common cause of seizures in adults (18-35)
trauma, alcohol withdrawal and brain tumor
Kluver-Bucy syndrome (amygdala)
hyperphagia, hypersexuality, hyperorality and hyperdocility
SSRIs

(fluoxetine, sertraline, paroxetine, citalopram, escitalopram)
indications: depression and anxiety; first line for generalized anxiety disorder, OCD and PTSD

side effects: nausea, GI upset, somnolence, sexual dysfunction, tremor, diarrhea, and agitation

SEROTONIN SYNDROME: if SSRIs are used with MAOIs - fever, myoclonus, mental status changes, cardiovascular collapse
buspirone
indications: generalized anxiety disorder, OCD and PTSD

side effects: seizures with chronic use, no tolerance, dependence or withdrawal
TCA toxicity
convulsions, coma and cardiac arrythmias
Atypicals (for psych)

Buproprion, venlafaxine, Mirtazapine, Nefazodone and Trazodone
indications: depression, anxiety and chronic pain
side effect of Bupropion
decreased seizure threshold; minimal sexual side effects; CONTRAINDICATED IN BULIMICS
side effects of venlafaxine
diastolic hypertension
side effect of Mirtazapine
atypical

weight gain, sedation
side effects of Nefazodone
atypical

sedation, HA and dry mouth
side effects of Trazodone
aytpical

highly sedating, priapism
TCAs

nortriptyline, desipramine, amitriptyline and imipramine
indications: depression, anxiety disorder, chronic pain, migraine and enuresis (imipramine)

side effects:

LETHAL with OD owing to cardiac arrhythmias...monitor for 3-4 days in the ICU after OD

ANTICHOLINERGIC EFFECTS - dry mouth, constipation, urinary retention and sedation
phenelzine and tranylcypromine
MAOIs

indication: depression, especially atypical

Side effects - hypertensive crisis if taken with high-TYRAMINE foods (cheese, red wine)

sexual side effects, orthostatic hypotension, weight gain
chronic lithium use...
hypothyroidism and nephrotoxicity
lamotrigine can lead to a...
life threatening skin rash
Typical antipsychotics

haloperidol, droperidol, fluphenazine, thioridazine, chlorpromazine
indications: psychotic d/o, acute agitation, acute mania and Tourette's syndrome

side effects:

EPS!!!
HYPERPROLACTINEMIA
ANTICHOLINERGIC EFFECTS - drug mouth, urinary retention and constipation

seizures, hypotension, sedation and QTc prolongation
side effect of Thioridazine
typical antipsychotic

irreversible retinal pigmentation
Neuroleptic malignant syndrome
fever, muscle rigidity, autonomic instability, clouded consciousness

stop medication, go to ICU

Dantrolene or bromocriptine
Atypical antipsychotics

clozapine, risperidone, quetiapine, olanzapine, ziprasidone and aripiprazole
indicaitons: 1st line for schizophrenia - fewer EPS and anticholinergic effects

Clozapine is reserved for severe tx resistance and severe tardive dyskinesia; AGRANULOCYTOSIS

side effects of atypicals: weight gain, Type 2 DM, somnolence, sedation and QTc prolongation
Lithium toxicity
ataxia, dysarthria and delirium
Lithium
mood stabilizer, used for acute mania (in combo with antipsychotics); prophylaxis in bipolar disorders and augmentation in depression tx

side effects: thirst, polyuria, diabetes insipidus, tremors, weight gain, hypothyroidism, nausea, diarrhea, seizures, teratogenicity (if used in first trimer), acne and vomiting
Carbamazepine
2nd line mood stabilizer; anticonvulsant

side effects: nausea, skin rash, leukopenia, AV block

rarely, aplastic anemia (monitor CBC biweekly), Stevens-Johnson syndrome
Valproic acid
bipolar d/o and anticonvulsant

side effects: GI (N/V), tremor, sedation, alopecia, weight gain

rarely - pancreatitis, thrombocytopenia, fatal hepatotoxicity and agranulocytosis
Lamotrigine
2nd line mood stabilizer; anticonvulsant

side effects: blurred vision, GI distress, Steven Johnson syndrome
acute dystonia
involuntary muscle contraction or spasm (eg. torticollis, oculogyric crisis)

tx: anticholinergics (benztropine or diphenhydramine); to prevent, administer these meds prophylactically
akathisia
subjective/objective restlessness - perceived as being distressing

tx: decrease neuroleptics and try beta-blockers (propranolol)

benzos or anticholinergics may help
Dyskinesia
pseudoparkinsonism (eg. shuffling gait, cogwheel rigidity)

tx: give an anticholinergic (benztropine) or a dopamine agnost (amantadine); decrease dose of neuroleptic or d/c
Tardive dyskinesia
stereotypic oral facial movements...likely from dopamine receptor sensitization...often irreversible (50%)

tx: d/c or decrease dose of neuroleptic; consider changing neuroleptic (to clozapine or risperidone)

GIVING ANTICHOLINERGICS OR DECREASING NEUROLEPTICS MAY INITIALLY WORSEN TARDIVE DYSKINESIA
evolution of EPS
4 hours: acute dystonia

4 days: akinesia

4 weeks: akathisia

4 months: tardive dyskinesia
Cluster A personality d/o
weird...

paranoid, schizoid (loner) and schizotypal
Cluster B pers d/o
wild...

Borderline, histrionic, narcissistic and antisocial
Cluster C pers d/o
worried and wimpy

obsessive compulsive, avoidant and dependent
Rett's disorder
genetic neurodegenerative d/o of FEMALES with progressive impairment (language, head growth, coordination, ataxia, seizures, MR) AFTER 5 MONTHS NORMAL DEVELOPMENT
Childhood disintegrative disorder
severe developmental REGRESSION after > 2 years of normal development (eg. language, motor skills, social skills, bladder/bowel control, play)

males > females
Tourette's syndrome
a/w ADHD, learning disorders and OCD

multiple motor tics (blinking, grimacing) and vocal tics, occurring many times a day, recurrently for > 1 year with social or occupational impairment

tx: dopamine receptor antagonists (haloperidol, pimozide) or clonidine...stimulants can worsen or precipitate tics
substance dependence
tolerance

withdrawal symptoms

attempts to cut down use or abstain - fails

(dependence differs from abuse b/c has physical manifestations)
alcohol withdrawal
tremor, tachycardia, hypertension, malaise, nausea, seizures, DTs and agitation
opiod intoxication
euphoria leading to apathy, CNS depression, constipation

PUPILLARY CONSTRICTION and respiratory depression (life-threatening OD)

naloxone/naltrexone will block opioid receptors and reverse effects (beware of antagonist clearing before opioids...particularly long-acting opioids like methadone)
opioid withdrawal
dysphoria, insomnia, anorexia, myalgias, fever, lacrimation, diaphoresis, dilated pupils, rhinorrhea, piloerection, nausea, vomiting, stomach cramps, diarrhea and yawning
amphetamine intoxication
PUPILLARY DILATION, psychomotor agitation, impaired judgment, HTN, tachycardia, fever, diaphoresis, anxiety, angina, euphoria...arrhythmias, hallucinations, seizures

can give haldol for severe agitation and symptom targeted meds (like antiemetics, NSAIDs)
amphetamine withdrawal
postuse "crash" with anxiety, lethargy, HA, stomach cramps, hunger, fatigue, depression/dysphoria, sleep disturbance, nightmares
PCP intoxication
ASSAULTIVENESS
VERTICAL/HORIZONTAL NYSTAGMUS

belligerence, psychosis, violence, impulsiveness, psychomotor agitation, HTN, impaired judgement, ataxia, seizures, delirium

give benzos or haldol for severe symptoms
PCP withdrawal
may have recurrence of intoxication symptoms due to reabsorption in the GI tract; udden onset of severe, random violence
galactorrhea, impotence, menstrual dysfunction and decreased libido
patient on dopamine antagonist
key side effects of atypical antipsychotics
weight gain, type 2 DM and QT prolongation
a young wt lifter receive IV haldol and complaints that his eyes are deviated sideways...dx? tx?
acute dystonia (oculogyric crisis); tx with benztropine or diphenhydramine
med to avoid in pts with history of alcohol withdrawal seizure
neuroleptics
5 month old girl has decreased head growth, truncal dyscoordination and decreased social interaction
Rett's disorder
violent patient with horizontal and vertical nystagmus
phencyclidine hydrochloride intoxication (PCP)
man has repeated, intense urges to rub his body against unsuspected passengers on a bus
frotteurism (a paraphilia)
live, attenuated vaccines
MMR, polio (sabin), yellow fever
Inactivated (killed) vaccines
cholera, influenza, HAV, polio (Salk) and rabies
Toxoid vaccine
diphtheria, tetanus
Subunit vaccines
HBV, pertussis, Streptococcus pneumoniae, HPV, meningococcus
Conjugate vaccines
Hib, Strep pneumoniae
number of true positives divided by number of patients with the disease
sensitivity
sensitive tests have few false negatives and are thus used to...
rule OUT a disease
cross sectional survey - incidence or prevalence?
prevalence
cohort study - incidence or prevalence
incidence and prevalence
case control study - incidence or prevalence?
neither
difference btw cohort and case-control study
cohorts can be used to calculate relative risk, incidence and odds ratio

case control studies used to calculate odds ratio
attributable risk?
incidence ratio of a disease in exposed minus IR of disease in unexposed
Relative risk?
incidence rate of disease in population exposed to facor divided by incidence rate of those not exposed
Odds ratio?
likelihood of a disease among individuals exposed to a risk factor compared to those who have not been exposed
number needed to treat?
1 / (rate in untreated group - rate in treated group)
patients where screening for colorectal cancer is initiated early...
patients with IBD, those with FAP/hereditary nonpolyposis colorectal cancer, and those who have first degree relatives with adenomatous polyps (< 60 years old) or colorectal cancer
percentage of cases within one SD of the mean? two SDs? three SDs?
68%

95.5%

99.7%
postnatal mortality?
number of death from 28 days to one year per 1000 live births
infant mortality?
number of deaths from birth to one year of age per 1000 live births (neonatal + postnatal mortality)
perinatal mortality?
number of deaths from 20 weeks' gestation to one month of life per 1000 total births
maternal mortality?
number of deaths during pregnancy to 90 days postpartum per 100,000 live births
involuntary psychiatric hospitalization can be undertaken for which three reasons?
danger to self, danger to others or gravely disturbed (unable to provide for basic needs)
when can a physician refuse to continue treating a pt on grounds of futility?
no rationale for treatment, maximal intervention is failing, given intervention has already failed and tx will not achieve goals of care
conditions where confidentiality can be overriden...
real threat of harm to third parties, suicidal intentions, certain contagious diseases; elder and child abuse
10 yr old child presents in status epilepticus, but parents refuse tx on religious grounds...
tx because disease represents immediate threat to the child's life...then seek a court order