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811 Cards in this Set

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Term
Association
Notes
Orientia tsutsugamushi
black eschar, rash on trunks that spreads to extremities, chigger borne
Formerly Rickettsia tsutsugamushi
Chlamydia trachomatis
cell wall lacks muramic acid
Reiter's Syndrome
Urethritis, conjunctivitis/uveitis, arthritis
Yersinia pestis
antiphagocytic components F1 and VW
F1 and VW are active at 37C, which is why they are not virulent in the flea vector (25C)
Type 3 Secretion System (T3SS)
sensory probes used to detect presence of eukaryotic organisms, help bacteria infect
Shigella, Salmonella, Yersinia, Chlamydia, Pseudomonas, EHEC
Red man syndrome
Vancomycin
also ciprofloxacin, amphotericin B
sporotrichosis
rose thorns, gardeners
subcutaneous nodules that ulcerate and travel along lymphatics
Histoplasma
bird and bat droppings in mississippi and ohio
granulomas with calcifications on CXR
Progressive supranuclear palsy
widespread neuronal loss and gliosis in subcortical sites
Middle meningeal artery
found in middle cranial fossa
Toxoplasmosis
poorly cooked pork
Mucor and Rhizopus
>90 degree branching, ketoacidotic diabetics
Buproprion
seizures in bulimic or anorexic patients
Torticollis
involuntary twisting or devation of the neck, neck pain, sensory tick, abnormal head posture
acute or delayed complication of dopamine antagonist therapy (antipsychotics)
Organ of Corti
Contains hair cells that can be damaged by loud sounds
Atherosclerosis of brain vessels
commonly found in circle of willis, NOT in penetrating smaller arteries
Subdural hematoma
negative initial workup at time of trauma, delayed onset of symptoms (2 weeks), originates from bridging veins
Internal branch of superior laryngeal nerve
supplies sensory innervation to laryngeal mucosa above vocal cords
runs with superior laryngeal artery
Subacute sclerosing panencephalitis
caused by perinatal measles (rubeola) infection, manifests in childhood, teenager and leads to death
Prions
acute presentation of progressive ataxia and dementia, spongiform change
encephalopathy with axonal degneration, neuronal loss, gliosis, astrocytic proliferation
Cushing reflex
HTN and bradycardia due to increased ICP
autonomic response triggered by changes in the arterial-to-intracranial pressure gradient
xerostromia
Dry mouth
Amide analgesics
Have 2 "I's" in name
Trihexyphenidyl
muscarinic antagonist
used as adjunctive therapy in Parkinson disease
Amitriptyline
Strong anticholingergic effects
useful in depression and parkinsons
vincristine
peripheral neuropathy
anterior ear canal innervation
auriculotemporal nerve
posterior half of ear canal innervation
auricular branch of vagus
both surfaces of lower auricle
great auricular nerve
cranial surface of upper auricle
lesser occipital nerve
viral encephalitis
arthropod transmission during summer
Blowout fracture
maxillary sinus blood
Prosopagnosia
can't recognize faces
cryptococcus
latex particle agglutination
nerve growth
1 mm/day
Lithium
hypothyroidism
check TSH every 1 to 2 months
Vecuronium
ACh antagonist
reverse blockade with neostigmine
Ki-67
stains astrocyte neoplasms
acanthamoeba
free living amoeba that infects brain, usually in immunosuppressed
cyclobenzaprine
centrally acting skeletal muscle relaxant
structurally related to TCAs, has anticholingergic side effects
schwann cells
axonal regeneration
toxoplasmosis
ingestion of cysts in meat
Pick's disease
similar to AD, but with frontotemporal atrophy
REM sleep decrease
medication that causes decrease in ACh
piriform cortex
primary olfactory cortex
receives neurons from olfactory bulb
Glaucoma (closed angle)
painful, bluurred vision w/ halos around eyes
treat with IV acetazolemide
Y. pestis
prophylaxis is doxycycline, treatment is streptomycin or gentamycin
lymphogranuloma venerum
C. trachomatis L1-L3, fluctuant draining nodules
Thiamine deficiency
Wernicke-Korsakoff, Dry beriberi (polyneuritis), wet beriberi (cardiomyopathy)
HIV encephalitis
multinucleated giant cells
S. pneumoniae attachment
IgA protease cleaves IgA into Fc, which attaches to bacterium and allows attachment to Fc receptors on mucosal cells
Phenylethanolamine=N-methyltransferase (PMNT)
converts NE to E
Halothane
hepatitis w/ focal massive necrosis
Cowdry Type A inclusions
HSV-1 encephalitis, intranuclear viral inclusion bodies
HSV-1
most common cause of fatal, sporadic encephalitis cases in US
area postrema
floor of 4th ventricle, responds to chemical signals, vomit center
Alar plate
dorsal spinal cord
sensory or afferent portion
basal plate
ventral part of spinal cord
motor or efferent portion
AChE inhibitors
carbamylate AChE
often combined w/ prednisone to treat severe MG
Pinealoma
Parinaud syndrome (epward gaze palsy, light and accomodation deficit, failure of convergence
Herpes zoster encephalitis
Encephalitis + shingles
resistant to acyclovir
General paresis
general paraylsis of the insane, includes mental deterioration that precedes motor system deterioration
late sequela of syphilitic infection
sagittal sinus thrombosis
associated with hypercoagulable states
increased frequency during prego/postpartum
Taenia solium
cysticercosis, can invade CNS (neurocysticercosis)
parasitic infection by ingesting eggs in pork, found in south america and central america
Cerebellar abscess
otitis media is #1 cause
Pituitary surgery
approach via the sphenoid sinus transnasally
Thyroglossal duct
thyroid gland
failure of the duct to degenerate may lead to a thyroglossal duct cyst or a median cervical cyst
Retinal angiomas
Von hippel-lindau disease
Nerve in tonsillar fossa
glossopharyngeal nerve
Bartonella henselae
cat-scratch disease
stellate granulomas w/ central necrosis and gram neg organisms
Target cells
thalassemia, hemoglobin C disease, liver disease
Reed-sternberg cell
somatic hypermutation, CD15, CD30
Nodular sclerosis hodgkin's lymphoma
fibrotic bands
Mast cells
release histamine, serotonin, leukotrienes, platlet aggregating factor (PAF)
Giemsa stain = metachromasia of cytoplasm, granular cytoplasm
Lines of Zahn
cell-rich layers found in a thrombus that forms pre-mortem
post-mortem clots will not have lines of zahn
Spontaneous bleeding
20,000 platelet count
E. coli K1 capsule
neonatal meningitis
Listeria and GBS are other common causes of neonatal meningitis
Hepatocellular carcinoma
erythropoietin overproduction -> polycythemia
increased EPO is also associated with RCC and hemangioblastoma
Burkitt Lymphoma
t(8;14), t(8;22), t(2;8)
Febuxostat
xanthine oxidase inhibitor
given in conjunction with chemotherapy for leukemias and lymphomas to prevent hyperuricemia
Sulfa drugs + hemolytic anemia
G6PD
Schuffner dots
multiple brick-red dots in Romanovsky-stained blood smears
P. vivax occurs in western hemisphere
Clarithromycin
inhibits hepatic enzymes
if given with warfarin, enhances activity and may lead to anticoag and hematuria
G6PD hemolytic drugs
antimalarials, dapsone, sulfonamides
Decreased ESR
sickle-cell, polycythemia, CHF
Increased ESR
increased antibody formation: cancer, infection, prego, connective tissue diseases
Smudge cells
CLL
older individuals, indolent
cirrhosis and coag factors
If d-dimer is increased, that means that fibrin is still being made and that the real reason for a decrease in coag factors is consumption and not the cirrhosis
FDPs vs. d-dimer
FDP can be generated from degradation of fibrinogen or fibrin, while D-dimer derives exclusively from fibrin
FDP can be elevated due to plasmin-mediated breakdown of fibrinogen (primary fibrinolysis). Elevated FDP isn't enough for DIC. You must also have and increased D-dimer. People with cirrhosis can have decreased plasmin inhibiting proteins and this would lead to an increased FDP, which could incorrectly be diagnosed as DIC
DIC
exposure to lots of tissue factor over a brief period of time
Celecoxib
COX-2 inhibitor
used for pain management, contraindicated in sulfa allergy and coronary disease
Pirioxicam
indicated for moderate to severe pain associated with inflammatory disease
TdT (terminal deoxynucleotidyl transferase)
mediates N-nucleotide addition to junctions in gene segments
very primitive cell marker that is active when VDJ rearrangement occurs
Cytoplasmic mu chains
positive cells have completed VDJ rearrangement
Babesia microti
causes babesiosis transmitted by the Ixodes tick
B. burgdorferi and Ehrlichia phagocytophila are also trasnmitted by the Ixodes scapularis tick
P-450 inducers
quinidine, barbiturates, St. John's wort, Phenytoin, rifampin, griseofulvin, carbamazepine, chronic alcohol use
Queen Barb Steals Phen-phen and Refuses Greasy Carbs Chronically
P-450 inhibitors
sulfonamides, isoniazid, cimetidine, ketoconazole, erythromycin, grapefruit juice, acute alcohol use
Inhibit yourself form drinking beer from a KEG because it makes you Acutely SICk
Epstein-Barr virus
infects B-cells by attaching to CD21 receptor
cells that predominate in the blood during a EBV infection are CD8+ T-cells
Chloroquine
contraindicated in malarial patients with psoriasis
may lead to chloroquine retinopathy
Malaria treatment
Chloroquine is first choice, atovaquone/proguanil is alternative treatment
Eosinophil granules
crystalline core contains major basic protein (destroys parasites)
light component around the dense crystalline core contains histaminase, arylsulfatase, and other enzymes
Gamma-carboxyglutamate residues
vitamin K deficiency prevents gamma-carboxyglutmation and thus a deficiency in clotting factors
Brushfield's spots
white speckling of the iris
associated with Down Syndrome. Down syndrome also increases risk of VSD, ASD, ALL, Alzheimer's, duodenal atresia
TGF-β
stimulates production of basophils and suppresses production of eosinophils
Neurofibromin gene (chromosome 17)
inhibits p21 ras oncoprotein
mutation leads to neurofibromatosis type 1
Merlin gene (chromosome 22)
regulator of contact-dependent inhibition of proliferation
mutation leads to neurofibromatosis type 2
Downey Type II Cells
large, basophilic, vacuolated T-cells
associated with EBV
Bone marrow expansion in calvarium
sickle-cell, thalassemia
Treatment of neonatal jaundice
Phototherapy (light decomposes bilirubin) and riboflavin
Warfarin overdose
Both extrinsic and intrinsic pathways are affected
normally, during warfarin treatment, only PT is prolonged because factor VII is the only factor that is decreased enough to impair coag
Streptokinase
binds to and activates plasminogen
DiGeorge Syndrome
Patients present with tetany (hypocalcemia due to hypoPTH), recurrent infections, lack of type IV hypersensitivity
CATCH-22: Cardiac abnormality, Abnormal facies, Thymic aplasia, Cleft palate, Hypocalcemia, deletion on chromosome 22
Cat-scratch fever
painful, enlarged lymph node w/o fever
biopsy of node shows granulomas with necrotic debris
Uterine leiomyomas
blood loss during menstruation leads to iron deficiency anemia
extracellular bacterial infection
high white count with left shift
Birbeck granules
Langerhans cell histiocytosis
Heterophile antibody test
diagnostic test for EBV/mononucleosis
another word for monospot
EBV
nasopharyngeal carcinoma, African form of Burkitt lymphoma, B-cell lymphoma
French-American-British classification
L for lymphoblastic, M for myeloblastic
1 for small uniform nuclei and scant cytoplasm, 2is variable lymphoblasts with irregular nuclei and more cytoplasm
Hemoglobin A2
B-thalassemia minor
ABO incompatibility
Mother is O and infant is A or B. Normally, IgM is produced by mother, but rarely, IgG can be produced and can cross the placenta
mild anemia, jaundice, + coombs test
ticlopidine
severe bone marrow toxicity
same mechanism as clopidogrel (inhibit ADP receptor)
Polycythemia vera
can progress to essential thrombocytosis and myelofibrosis, but does not progress to CML
ergonavine
triggers vasospasm in susceptible patients, use with angiography to diagnose prinzmetal angina
baclofen
treat spasticity
used in dystonia, symptomatic MS
Waldenstrom's macroglobulinemia
cancer of lymphocytes
IgM spike, no bone lytic lesions, hyperviscosity syndrome
Xanthoma
lipid laden histiocytes seen in hyperlipidemia (Touton cells)
Variceal rupture
engorgement of the azygos vein and the left gastric vein
Atropine
leads to rapid pulse with no change in blood pressure
Lyme disease
AV block
Temporal arteritis
focal granulomatous inflammation
Coarctation
rib notching, hypertension due to underperfused kidneys (RAAS activation)
occurs distal to the left subclavian artery near the region of the ductus arteriosus
Loeffler endocarditis
restrictive cardiomyopathy, prominent eosinophilic infiltrate
Isolated elevated AST
myocardial infarction
Transposition of great vessels
keep PDA open with PGE1 analog like alprostadil or misoprostal
PDA shunt must be open to keep oxygenated blood circulating
VEGF
secreted under hypoxic conditions by cells, such as muscle during exercise
levels rise to high levels within an hour after exercising
Arteriolar rarefaction
loss of arterioles (decreased arteriolar density) seen in severe hypertension
Capillary wall-to-lumen ratio
never changes because capillaries don't have smooth muscle in their walls
Tenecteplase, alteplase
tPA
Beta thalassemia major
large numbers of transfusions lead to iron overload and hemosiderosis, which eventually leads to cardiac failure
Medial umbilical arteries
arise from internal iliac arteries
Guarnieri bodies (type B inclusions)
diagnostic for poxvirus
poxvirus is the only DNA virus to replicate entirely in the cytoplasm
koilocytic atypia
squamous epithelial cells with characteristic cytoplasmic vacuoles
HPV
Severing of IX and X
tachycardia w/ hypertension
illusion that the patient has lost all blood pressure leads to increase in sympathetic stimulation
Propranolol
blunt or prevent the premonitory signs and symptoms (hunger, tachycardia, fatigue, tremors) or hypoglycemia
nonselective beta-blockers may even potentiate insulin-induced hypoglycemia
hyperplastic arteriolosclerosis
"onion-skinning" in vessel walls due to progressive laying down of fibrotic tissue by smooth muscle cells
Procainamide
reversible SLE, prolonged QT
contraindicated in long QT syndrome
Charcot-Bouchard
intracerebral hemorrhage
mostly found in small perforating vessels of the brain (lenticulostriate)
Berry aneurysm
subarachnoid hemorrhage
blood metabolites can lead to vasospasm
valproic acid
hepatotoxicity, neural tube defects in fetus
Type II pneumocytes
lamellar bodies which contain the surfactant
Hemoptysis
rupture of bronchial veins due to left heart failure
Mucor
epistaxis, severe facial sinus infection, frontal lobe abscess
DKA and leukemia
Corynebacterium diptheria
grow on tellurite agar, look for gram positive rod with metachromatic granules
Hirano bodies
intracytoplasmic proximal dendritic eosinophilic inclusions composed of actin
seen in AD
Transposition of the great vessels
associated with maternal diabetes
Thiazide diuretics
drug-induced gout
Spironolactone
blocks androgen receptors, leading to gynecomastia (can use eplerenone instead, because it's a more specific aldosterone receptor antagonist)
potassium sparing duiretic that is a competitive inhibitor of aldosterone receptors in the DCT
Contractility of heart
demonstrated by slope of graph…
increased by beta-1 agonists
Muscarinic cholinergic receptor antagonist
increases heart rate without changes in MAP
Marfan
defect in fibrillin
ACE inhibitors
delay progression of CHF by protecting ventricles from remodeling
first line treatment for CHF, HTN w/ diabetes, renal problems
Indomethacin (NSAIDS)
precipitate acute renal failure
decrease prostaglandin synthesis, which primarily affects the afferent arteriorle, leading to vasoconstriction
beta blockers
can cause AV block
Rheumatic heart disease
fibrous bridging between valve leaflets and calcifcation, "fish-mouth" appearance
Calcification of mitral annulus
beadlike calcifications of the annulus in elderly individuals
Tiny vegetations along the line of closure of the valve leaflet
marantic (nonbacterial thrombotic) endocarditis
marantic endocarditis: sterile vegetations as a result of a pro-coag effect from tumors of the colon and pancreas
Indapamide
non-thiazide diuretic which acts like thiazide, lead to decreased Ca in urine
indapamide, hydrochlorothiazide, metolazone are used in volume overloaded states and HTN
Digoxin
life-threatening cardiac dysrhythmias (paroxysmal supraventricular tachycardia)
CHF
S3 sound on auscultation
Amlodipine
Ca-channel blocker, works on smooth muscle
used for treatment of mild to moderate HTN and angina
Left dominant coronary arteries
PDA is supplied by the left CFX
infarction leads to ischemia of the posterior septum and posterior left ventricle
Anemia
increased stroke volume and cardiac output to make up for the low levels of Hb
Neutrophil granule contents
myeloperoxidase, lactoferrin, hydrolytic enzymes
Granulomatosis infantisepticum
vaginal transmission of listeria to neonate leads to early-onset sepsis or neonatal meningitis
formation of fatal granulomas
Enterococcus faecium
More likely to be resistant to vancomycin, less common than E. faecalis
ethambutol
red-green color blindness
Isoniazid, pyrazinamide
must be activated by bacterial enzymes from prodrug form
Chlorthalidone
thiazide diuretic
Persistent truncus arteriosus
goes along with a VSD, because the conotruncal ridges that are malformed in the truncus also give rise to the interventricular septum
Adult polycystic kidney disease
Give ACE inhibitor to treat HTN
the cysts impair perfusion of glomeruli, which triggers the secretion of renin by the juxtaglomerular complexes
QRS complex prolongation
can occur due to bundle branch block, which can be a result of coronary artery occlusion
Cystic hygroma
assoicated with Turner syndrome
Turner also associated with coarctation, aortic stenosis, webbed neck, lymphedema of the extremities, short stature, gonadal dysgenesis, hypothyroidism, and infertility
Rib notching
found in coarctation, due to anterograde flow through the intercostal artery via the subclavian (first intercostal artery) or internal thoracic artery (subsequent intercostal arteries)
Venous drainage of ovary
Right ovary: drain into pampiniform plexus, right gonadal (ovarian) vein, IVC
Left ovary: drain into pampiniform plexus, left gonadal (ovarian vein), left renal vein, IVC
Central hemorrhagic necrosis of hepatic lobules
CHF
mottled appearance (nutmeg liver)
Minoxidil
opens K-ATP channels and hyperpolarizes the membrane, resulting in relaxation of vascular smooth muscle
also hyperpolarizes pancreatic beta cells, leading to a decrease in insulin secretion in response to glucose
Aortic stenosis
increase in diastolic blood flow
AS causes an increase in systolic pressure in the LV, compressing the coronary arteries even further, thus making it necessary to increase blood flow during diastole even more so that in a normal heart
AA Amyloid
assoicated with chronic inflammatory disease
AE Amyloid
assoicated w/ medullary carcinoma of the thyroid and pancreatic islet cell adenomas
AE amyloid is not systemically distributed, but found directly in the neoplasm
AF Amyloid
assoicated w/ certain familial amyloidosis syndromes
distributed within peripheral nerves and kidney and senile cardiac amyloidosis in elderly
AL Amyloid
associated w/ myeloma and B-cell malignant lymphomas
produced by neoplastic cells which deposit in heart, GI, kidney, spleen, tongue
Septic pulmonary edema
due to increase vascular permeability
Peaked T-wave
hyperkalemia
Constrictive pericarditis
kussmaul sign, pericardial knock
usually due to TB or pyogenic staph infections
kussmaul sign
increase in systemic venous pressure on inspiration, due to impaired filling of the right ventricle
Long QT syndrome
don't use drugs that prolong QT, cause hypokalemia, or hypomagnesemia
agents that prolong QT include procainamide, sotalol, amiodarone, disopyramide, dofetilide, phenothiazines, and TCAs
patent ductus arteriosus
indomethacin to close, alprostadil (prostaglandin) to keep open
Complete heart block (third degree heart block)
ventricles beat independently of SA node activity and do not correspond to P waves
heart rate is usually 30-40 bpm. Stroke volume is increased so that CO remains constant to keep a constant BP, but pulse pressure still goes up a bit because SV increases
Paraganglioma
most often found in adrenal glands (pheochromocytoma), but most common extra-adrenal is carotid body tumor
catecholamines are the major secretory products (norepinephrine for non-adrenal, epinephrine for adrenal)
Carotid body hyperplasia
people living at altitude/high mountains
Congenital rubella
triad of PDA, cataracts, sensorineural deafness
Prego mother with rubella has classic postauricular and suboccipital lymphadenopathy
Coxsackievirus A
herpangina (mouth blisters), acute hemorrhagic conjunctivitis, hand-foot-mouth disease
both Coxsackie A and B cause aseptic meningitis and the common cold
Coxsackievirus B
myocarditis, pericarditis, pleurodyna, Bornholm disease (Devil's grip), hepatits
both Coxsackie A and B cause aseptic meningitis and the common cold
Bornholm disease
pleurodyna, often caused by coxsackie B, where there is severe pain in the lower chest, often on a specific side
Reovirus
only double stranded RNA virus (dsRNA)
Hantavirus
rodent borne virus (robovirus), unlike other bunyaviridae which are arthropod borne (arbovirus)
hemorrhagic fever and Hantavirus pulmonary syndrome (HPS): endothelial injury leads to edema in lungs and can lead to hypovolemic shock
Clonidine
centrally acting alpha 2 agonist that works at the locus ceruleus to inhibit NE release
Dextramethorphan
used for cough suppression
opioid
Meperidine
anti-ACh properties and pro CNS seizure activity
Beaded pattern on angiography
fibromuscular dysplasia
common cause of renovascular stenosis in women (renal bruits on examination)
Atherosclerosis w/ foci of calcification
indicates severe atherosclerotic disease
Buerger disease
recurrent inflammatory disorder that causes thrombosis in extremities
associated with heavy smokers
metoprolol
dyslipidemia
Other beta blockers can cause AV block
Serotonin syndrome
hyperthermia, muscle rigidity, cardiovascular collapse, flushing, diarrhea, seizures
treat with cyproheptadine
Capillaries
largest cross-sectional area of any vessel in the body
translates to slowest flow through the vessels compared to other vessels
Furosemide
can lead to problems if used with Digoxin
furosemide leads to hypokalemia, which can exacerbate the effects of digoxin
Fully compensated coarctation
blood flow below and above the coarct are no different than a normal person
check pulses to see if the resistance has changed (increased pulse = increased resistance)
Endocardial cushions
migration of neural crest cells is required for proper development of the endocardial cushions
Abnormal migration of neural crest cells in Down syndrome leads to cardiac defects
Methemoglobinemia
treat with methylene blue (enhances conversion of methemoglobin to hemoglobin by increasing activity of enzyme methemoglobin reductase) or ascorbic acid
methemoglobinemia can be caused my excessive adminstration of nitric oxide (NO) because the NO reacts with hemoglobin to produce methemoglobin
Intense, static exercise
skeletal muscle contracts, compressing the vessels, leading to decreased blood flow and increase vascular resistance
dynamic, endurance exercise
skeletal muscles relax after contraction allowing the vessels to dilate, leading to increased blood flow and decreased vascular resistance
Dressler's syndrome
fibrinous pericarditis
Acebutolol, pindolol
Beta blocker with intrinsic sympathomimetic activity
not good for patients with angina because it may exacerbate it, or patients with thyrotoxicosis
Hypertension in pregnancy
Methyldopa (converted to alpha-methylnNE, which stimulates alpha-2 receptors centrally and leads to decreased sympathetic outflow)
MSFP
a measure of the "tightness" with which the circulatory system is filled with blood
MSFP increases with more blood in the system and it's easier for blood to flow into the heart, which tends to increase venous return
Graft vascular disease, graft arteriosclerosis
develops years after transplantation and is due to intimal thickening of coronary arteries without associated atheroma formation or inflammation
no chest pain because transplanted hearts are denervated
Niacin
decreases hepatic LDL and VLDL production
side effects: flushing, hepatotoxicity, tachycardia, hypoalbuminemia, hyperglycemia. Aspirin can help reduce the flushing
D-I-R-T
VMAT inhibitors: lead to decreased reuptake of monoamines into the presynaptic terminal, which allows them to be broken down by MAO, decreasing the monoamine signalling
Deserpidine, Ibogaine, Reserpine, Tetrabenazine
Eosinophilia
C-H-I-N-A: Connective tissue disease, helminthic infections, idiopathic hypereosinophilic syndrome, Neoplasia, allergies
Sphenopalatine artery
branch of the maxillary artery
artery of epistaxis
Suboccipital triangle
can gain access to the vertebral artery through this zone
Arteriosclerotic occlusive disease
classic symptom is claudication and impotence
decreased arterial pulse at the ankle because vessels are narrowed
Rheumatoid arthritis
Restrictive amyloid cardiomyopathy
Verapamil
assoicated with accelerated progression of CHF in certain patients
Reduviid bug
Trypanosoma cruzi
Chagas disease
Varicose veins
Exacerbated by chronically high venous pressure in the legs
Increased BUN, normal Creatinine
prerenal cause of azotemia, such as decreased renal perfusion
Kerley's lines
septal edema seen on chest radiograph
Heart failure cells
alveolar macrophages with hemosiderin residue
sputum has a rusty color
BNP (brain natriuretic peptide)
secreted from ventricles in response to volume expansion and pressure overload
useful in diagnosis of LHF (increased)
Arteriovenous fistula
high-output heart failure due to bypass of the microcirculation and increased venous return
causes: trauma from knife wound, surgical shunt for hemodialysis, mosaic bone in Paget's disease (where the bone vessels form microfistulas)
Hypercoagability
at it's peak in the morning hours
Prinzmetal angina
pathophys thought to be due to thromboxane A2 or an increase in endothelin
Myocarditis due to coxsackie
lymphocytic infiltrate with focal areas of necrosis
Superior vena cava syndrome
extrinsic compression of SVC, usually from primary lung cancer
puffiness and blue discoloration of the face, arms, shoulders, retinal hemorhage, stroke
Councilman bodies
Eosinophilic/acidophilic inclusions in hepatocytes indicating apoptotic death
Yellow fever, viral hepatitis
Viral Gastroenteritis
#1 is rotavirus, #2 is norovirus
Top 5 causes of pediatric red rash
Measles, rubella, scarlet fever, roseola, erythema infectiosum (parvovirus)
Spontaneous tendon rupture
flouroquinolones
HBV
polyarteritis Nodosa and glomerulonephritis
immune complex deposition
Sickle cell immunity against malaria
Immune to P. falciparum because of decreased oxygen content in cells and because of increased splenic destruction of sickled cells
Red man syndrome
side effect of vancomycin, due to direct stimulation of mast cells
give antihistamines before administration of vancomycin or enfuse slowly
Sulfonamides
Steven Johnson syndrome side effect
Ethacrynic acid
non-sulfa diuretic used for people with sulfa allergies
Thymine dimers
caused by UV radiation
inability to repair the defect results in xeroderma pigmentosum, UV sensitivity, excessive freckling, and early onset skin cancer (basal cell, squamous cell, melanoma)
Chronic granulomatous disease
NADPH oxidase deficient, which prevents formation of oxygen radical products
myeloperoxidase uses a product of NADPH oxidase, hydrogen peroxide, to make it's own toxic chemicals to kill bacteria
Velocardiofacial syndrome (DiGeorge Syndrome)
malformation of third and fourth pharyngeal pouches, leading to thymic aplasia and absence of parathyroids
may present with tetanus due to hypocalcemia
Recombinase A
product of the recA gene, necessary for recombination of a linear piece of DNA into the recipient cell's chromosome
F+ to F- conjugation is possibly because there is no transfer of linear DNA (only DNA transfer that doesn't require homologous recombination to occur)
Klebsiella pneumonia
lobar caviation
Reovirus
needs its own polymerase enzyme in order to be infectious
other similar viruses include all negative-sense RNA viruses, reovirus (dsRNA), poxvirus (replicates in cytoplasm) and retrovirus
Bruton x-linked agammaglobulinemia
no peripheral B cells (no CD19+), low levels of IgG
hyper-IgM Syndrome
IgM-producing B cells cannot receive the signal to isotype switch, leads to severe pyogenic infections early in life
Deficiency in TH cells that express CD40L
Dolichol
substrate for the synthesis of glycoproteins, such as albumin
Chronic rejection therapy
Downregulation of T-lymphocyte activity
Ascaris lumbricoides
posses one of the most potent allergens in nature
leads to type I hypersensitivity
Heterochromatin
densly packed DNA around histones seen when the cell is undergoing mitosis
indicative of replicating cells and possibly a high grade cancer
Unconjugated bilirubin
not filtered by the glomerulus because it is water insoluble
Anti-RNP antibodies
marker for Mixed connective tissue disease (MCTD)
joint pain, myalgias, pleurisy, esophageal dysmotility, skin disease
hemorrhagic cystitis
cyclophosphamide: aklylating agent that causes DNA crosslinking, treats non-Hodgkin lymphoma, breast cancer, ovarian carcinoma
cyclophosphamide also causes bone-marrow suppression
Neuroblastoma
childhood tumor of sympathetic nerves along paravertebral chain or adrenal medulla
1p deletion and N-myc translocation, associated with poorer prognosis
Mandibulofacial dysostosis
abnormally formed mandible, ears, and palate
due to abnormal development of the first and second parhyngeal arches
Hemochromatosis
increased total body iron stores and can set off airport metal detectors
Argyria
blue-skin pigmentation due to silver poisoning
Primidone
P450 inducer
Aldolase B (Fructose-1-phosphate aldolase)
autosomal recessive disorder of fructose metabolism that leads to accumulation of fructose-1-phosphate
accumulation of F1P inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia after ingestion of fructose
Aldolase reductase
reduces glucose to sorbitol and galactose to galactitol
pseudomyxoma peritonei
mucus producing tumor of ovary or appendix fills the peritoneal cavity
gamma-glutamyl transpeptidase
transports amino acids into cells
deficiency causes mental retardation, seizures, increased plasma and urine levels of glutathione
Serum sickness
caused by hypersensitivity to drugs: fever, urticaria, lymphadenopathy, arthralgias, Erythema multiforme in severe cases. Occurs 7-10 days after initial exposure because it takes that long for IgG generation
Tx: oral prednisone and diphenhydramine (for urticaria)
Filaria infection
body coats then with thin layer of IgE, triggering an eosinophil-mediated cytotoxicity and the release of vasoactive spasmogenic substrates form mast cells and basophils
Exfoliatin
proteolytic exotoxin produced by S. aureus that causes bullous impetigo and Staph scalded skin syndrome
cleaves desmogleins in desmosomes
Neurocysticercosis
swiss-cheese appearance on head CT
ingestion of T. solium eggs in food or water contaminated with human feces
C3b
product of the cleavage of C3, attaches to bacterial surfaces for opsonization by phagocytes (C3a binds to mast cells and basophils, leading to histamine release)
also involved in removal of immune complexes from serum
Sickle Cell in African Americans
due to natural selection because sickle cell individuals are resistant to malaria
Tamoxifen
used to treat ER+ breast cancers
side effect: endometrial carcinoma
selective IgA deficiency
most common immunodeficiency in US
increased atopic allergy, possibly because of the increased isotype switch to IgE
K-complex and sleep spindles
high amplitude single spike followed by trough, seen in stage 2 sleep
Ammonium chloride
used to treat amphetamine overdose
acidifies the urine and hastens amphetamine excretion
Desmoplasia
excessive fibrous tissue formation usually seen with malignant neoplasms
Sjogren syndrome
dry mouth (xerostomia), dry eyes (keratoconjuntivitis sicca, patients complain of "sand in eyes"), arthritis
autoantibodies anti-Ro (SS-A), anti-La (SSB), antinuclear, and RF
Celecoxib
selective COX2 inhibitor, involved in prostaglandins that are assoicated with inflammation and pain
cannot be used in patients with sulfa allergy
I-cell disease (inclusion cell disease)
lysosomal storage disorder due to failure of addition of mannose-6-phosphate to lysosome destined proteins
lysosomal proteins are secreted out of the cell. Leads to coarse facial features, clouded corneas, restricted joint movement, high plasma levels of lysosomal enzymes, often fatal in childhood
Cyclin-CDK complexes
see FA pg76
Daclizumab
monoclonal antibody against IL-2 receptor on activated T-cells
indicated for kidney transplant rejection prophylaxis along with cyclosporine and corticosteroids
Repeated blood transfusions
may lead to hemosiderosis
hemosiderin (coarse, golden-brown granules in cytoplasm of cells all around body)
17 year old wants to get off life support
parents cannot decide to stop the life support, so you must wait until the patient is of age and he can make the decision on his own
Permeability of molecules through lipid bilayer
CO2>O2>urea>glycerol>glucose>sodium
hypokalemic periodic paralysis
autosomal dominant, symptoms in first or second decade of life, severe muscle weakness, habitual high-salt diet, may be due to primary defect in calcium channels
during acute attacks: decreased serum potassium
Hyper-IgM Syndrome
multiple pyogenic infections at an early age
C3 deficiency
defects in opsonization of encapsulated bacteria and removal of immune complexes (increased risk for type III hypersensitivity)
Ornithine transcarbamylase deficiency
Lethargic, unwilling to eat, poorly controlled RR/body temp, seizures, abnormal body movements
Increased urine orotic acid levels, decreased serum citrulline levels, elevated plasma glutamine
Galactosemia
absence of galactose-1-phosphate uridyltransferase, autosomal recessive
accumulation of toxic substances (galactitol), leads to failure to thrive, juandice, hepatomegaly, infantile cataracts, mental retardation
Gamma-delta T-cells
only category of T-cells that do not require education and selection in the thymus; these cells are found mostly in submucosa and intraepithelial spaces and may play a role in protecting the epithelium
have gamma-delta chain, as opposed to the much more common alpha-beta receptors
Cleft lip
lateral maxillary prominence fails to fuse with the medial nasal prominence
Cleft palate
palatine shelves (maxillary prominences) fail to fuse with each othe ror the primary palate (fused medial nasal prominences)
Karyorrhexis
pyknotic nucleus undergoes fragmentation followed by complete lysis
abscess necrosis is termed liquefactive necrosis
PPD reaction
macrophages are the most abundant cells types (CD14 positive) because they are recruited there by cytokines released by TH1 cells
there are also T-cells
Acrodermatitis enteropathica
inherited zinc deficiency
Oxalate crystals in urine
ethylene glycol poisoning
Cytarabine
inhibits DNA polymerase
used for AML in conjunction with an anthracycline
Sublimation
diversion of unacceptable impulses into more acceptable ones
mother whose child died of a disease who becomes active in a state or national organization designed to help families with the disease
Graves disease
type II hypersensitivity
Hashimoto's thyroiditis
type IV hypersensitivity
Cretinism
mental retardation, protuberant abdomen, puffy face, enlarged tongue
lack of thyroid hormone in a developing child prevents normal growth hormone synthesis and secretion, leading to dwarfism
Measurement of body fluids
plasma volume measured with 125-I-albumin; extracellular fluid volume can be measured using inulin
interstitial volume = extracellular fluid - plasma volume
Ribozyme
RNA complex that breaks down mRNA
mycophenolate mofetil
inhibits purine synthesis (guanine) and lymphocyte proliferation
Perifollicular hemorrhage
vitamin C deficiency
HIV positive individuals
can only make IgM antibodies because of deficient CD4 cells
Homocystinuria
due to cystathionine synthase deficiency
mental retardation, long limbs, tall stature, kyphosis, increased plasma homocysteine and methionine levels
Azathioprine
inhibits de novo purine synthesis and interacts with allopurinol
Immunosuppression
knocks down t-helper 1 cells, as opposed to HIV, which knocks down t-helper 2 cells
first-order kinetics
a constant proportion of the target is killed by the drug
Clathrin
receptor-mediated endocytosis at the plasma membrane, transfer of lysosomal enzymes from trans-golgi
REM rebound
When the patient stops taking the drugs, there is an increase in the number and intensity of dreams for several days following discontinuation
barbiturates, alcohol, phenothiazines, and MAO inhibitors decreased the amount of REM sleep while the patient is taking them
Ecthyma gangrenosum
pseudomonas infection of the foot with a black, necrotic center and raised erythematous edges
seen in diabetics
obstructive sleep apnea syndrome
first line treatment: weight loss and use of continuous positive airway pressure
site-specific transduction
integration of a temperate phage, integration of a fertility factor, and movement and insertion of transposons…no idea what this means
Tongue fasciculations
werdnig-hoffman (spinal muscular atrophy)
hexagonal, benzene, staghorn crystals
cystinuria
cystine crystals precipitate in acidic urine, so treat with acetazolamide
Rheumatoid factor
anti-IgG antibody
Calreticulin, calnexin
chaperone proteins that assist in protein folding within in RER
problems at this stage lead to polyubiquination which leads to degredation by proteosomes
Early HIV infection
follicular dendritic cells in germinal centers of lymph nodes are important reservoirs of HIV
Interferon gamma
released by T-lymphocytes and activate macrophages
Bruton x-linked agammaglobulinemia
mutation in cytoplasmic tyrosine kinase (bruton tyrosine kinase, btk)
gene is important in driving pre-B cells to become mature B cells
pemphigus vulgaris
autoimmune disease with antibodies against desmoglein 1 and 3
acantholysis: intraepidermal bullae involving skin and oral mucosa. Positive Nikolsky's sign (separation of epidermis when touching skin)
F+ to F- conjugation
principal means of transfer of drug resistance genes on plasmids
common in gram-negative bacilli
Generalized transduction via bacteriophage
transfer of methicillin and vancomycin resistance between S. aureus and imipenem resistance in P. aeruginosa
Also seen in specialized transduction
Transformation
S. pneumoniae transfer of drug resistance
OCD
assoicated with tourette's and ADHD
ataxia telangiectasia
telangiectasias of the skin and eyes, variable immunodeficiency, progressive ataxia
mutation of ATM gene (tumor suppressor gene)
Neonatal hepatomegaly and hypoglycemic seizures
think glycogen storage disease
Fragile X syndrome
get trinucleotide repeat test for diagnosis, not karyotype (might not show the defective X chromosome)
Cherry-red spot on macula
w/ hepatosplenomegaly = Niemann-Pick; w/o hepatosplenomegaly = Tay-Sachs
Globoid cells
Krabbe's disease
NMDA channel
ligand-gated AND voltage-gated cation channel
Cachexia
reduction in lean body mass, profound loss of appetite and weakness due to TNF-alpha, interferon-gamma, IL-1
Long-chain acyl CoA dehydrogenase (LCAD) deficiency
hypokalemic kypoketosis that leads to cardiomyopathy in childhood
also see accumulation of carnitine esters (long chain acyl carnitines), which rules out carnitine uptake deficiency in the DDx
SCID
IL-2 receptor deficiency is most common cause
also caused by adenosine deaminase deficiency and inability to produce MHC-II molecules
Wiskott-Aldrich syndrome
exzema, thrombocytopenia, and immunodeficiency
IgE is frequently increased; mutation is in Wiskott-Aldrich serum protein (WASP) on X chromosome
Stomach cancer in Japanese
due to food preservatives and smoked foods
Opsonic antibody
IgG
represents past exposure to an antigen, levels of IgG persist much longer than IgM
IL-2
produced by T-helper cells and can be used to treat various types of cancer
increases numbers of cytotoxic T-cells and NK cells
Anticholinergic vs. stimulant overdose
anticholinergics = dry skin, stimulants = sweaty skin
migratory pulmonary infiltrates in asthmatic patient
allergic bronchopulmonary aspergillosis
MHC III
encodes for complement and tumor necrosis factors
T-cell independent B-cell activation
non-protein carbohydrate mediated (LPS) leads to cluster differentiation of B-cells
mitogen mediated activation of B-cells leads to a polyclonal response directed at everything except mitogens!
T-cell receptors
only recognize polypeptides that are displayed with MHC
J chain
holds together secreted IgA dimer and pentameric IgM
Secretory component or secretory piece
picked up by IgA in epithelial cells before it is secreted, prevents proteolytic cleavage of IgA
Decay Accelerating Factor (DAF)
also known as CD55
deficiency leads to paroxysmal nocturnal hemoglobinuria
Major Basic protein
can cause epithelial damage
released by eosinophils
Neuroblastoma
N-myc
Pneumocystis jiroveci diagnosis
Direct fluorescent antibody test
Bronchitis in smokers
Haemophilus influenzae, Legionella, or Moraxella
Megaloblastosis uncorrected with B12, folate
deficiency in orotidine decarboxylase or orotidine phosphoribosyltransferase
orotic acid crystals in urine (white needle-shaped crystals)
Sorafenib
multi-kinase inhibitor used for renal cell carcinoma
Bare lymphocyte syndrome
Type of SCID where cells are unable to synthesize and express MHC II
Omenn Syndrome
type of SCID where there is a nonsense mutation in genes involved in early VDJ recombination
Negative nitroblue tetrazolium test
Chronic granulomatous disease
Congenital Herpes Encephalitis
HSV-2 in children, while adult encephalitis is usually HSV-1
Tularemia
Francisella tularensis causes a rupturing pustule following by an ulcer with involvement of regional lymph nodes
Digoxin
binds to K+ site of Na/K ATPase
Mycobacterium avium intracellulare
treat with azithromycin
Peutz-Jeghers syndrome
widespread "freckles" (spots of melanin pigmentation)
associated with carcinomas of pancreas and colon, as well as other sites
Sacrococcygeal teratoma
contain derivatives of all 3 germ layers, which means it arose from the primitive streak (stage before 3 germ layers develop)
sacrococcygeal is most common tumor site
Transketolase
thiamine-requiring enzyme of non-oxidative half of hexose monophosphate shunt
activity is used as a clinical marker of thiamine deficiency, such as Wernicke-Korsakoff syndrome
Chocolate agar
H. influenzae
Charcoal yeast extract
Legionella pneumophila
Arthus Reaction
swelling and inflammation at inoculation site within a day
type III hypersensitivity
Fexofenadine
antihistamine that doesn't cause sedation because it doesn't cross the BBB
Fear of using public restrooms
social phobia
Salicylate intoxication
tinnitus is classified as the threshold symptom for intoxication
Duchenne and Becker Musuclar Dystrophy
usually due to deletions or insertions, not single based changes (missense or nonesense)
Marriage = emancipation
allowed to make own decisions for medical treatment, regardless of how old she is
C5a
neutrophil chemotaxis to an area of damage/inflammation
Keloid
due to excessive collagen deposition
surprisingly small number of fibroblasts
Warthin-Finkeldey (WF) giant cell
pathognomonic for measles or the live attenuated measles vaccine
Sirolimus
hyperlipidemia, thrombocytopenia, leukopenia
Lesch-Nyhan syndrome
defective HGPRT
buildup of monosodium urate because HGPRT is not around to recycle purine bases, so they just turn into uric acid instead
Pseudomonas culture
blue green on iron-limited environment, colorless on blood agar
Natural Killer (NK) cells
carry out extracellular lysis of infected cells that do not have MHC I (RBCs)
Adverse offects of oxytocin
hyponatremia, seizures, subarachnoid hemorrhage
metabolic alkalosis
causes deprotonation of albumin COOH, resulting in COO- that can bind free calcium. Results in decreased free calcium levels
Gynecomastia of puberty
common in adolescents, frequently asymmetric and tender, usually regress before 20 years old
only reassurance is needed, no fine-needle aspiration
Glucocorticoids
normally catabolic in muscle and adipose tissue, but increase glycogen synthesis and accumulation in the liver
Difference between primary and secondary Addison's
Primary has hyperpigmentation and hyperkalemia while secondary doesn't
Thyroid cancer w/ amyloid
Medullary thyroid carcinoma
Albrighty's hereditary osteodystrophy
kidney unresponsiveness to PTH (pseudohypoparathyroidism)
hypocalcemia, shorted 4th/5th digits, short stature
Tangier disease
due to deficiency in ABCA1 cholesterol transporter (normally takes cholesterol from peripheral cells and attaches it to HDL to be transported back to the liver)
characteristic yellow-orange tonsils, lymph node enlargement, hepatomegaly, sensory neuropathy and muscle wasting of the hands; serum cholesterol is low due to lack of HDL
Potassium iodide
administered after radiation exposure (Chernobyl): competes with the converted radioactive iodide for the iodide pump. If enough is taken, normal iodide will saturate the thyroid gland and the radioactive iodide will be excreted
Diabetic ketoacidosis
more 3-hydroxybutyrate is made compared to acetoacetate
plasma catecholamines and glucogon are usually increased due to a shift in metabolism to a starvation state
Thiazolidinediones (pioglitazone, rosiglitazone)
antidiabetic agent that increase insulin sensitivity, specifically peripheral tissues by release of adipokines
contraindicated in heart failure
Androgen insensitivity syndrome
defect in androgen receptor
phenotypically female w/ inguinal hernia, primary amenorrhea, external female genitalia, no uterus, lack of axillary and pubic hair
Renal osteodystrophy
secondary hyperparathyroidism due to renal failure
kidney can't excrete sufficient phosphate, which leads to PTH release, which increases bone resoprtion, leading to pathological fractures
MEN 2B
medullary carcinoma of thyroid, pheochromocytoma, oral and intestinal ganglioneuromatosis, marfanoid habitus
Chronic renal insufficiency
defect in renin production, leads to low aldosterone levels
Lab findings in thyrotoxicosis
increase in free and total T4, decrease in TSH
also increase in serum Ca2+ (bone tunover), increase in serum glucose (glycogenolysis), and decrease in serum cholesterol
Sabouraud's agar
culture fungi
Heterophil mononucleosis test
positive in EBV, negative in CMV
activating mutation in the Ca-sensing receptor of the parathyroid
hypothyroidism
Anti-glutamate decarboxylase antibodies
Type I diabetes
Osteoporosis prevention
raloxifene
human chorionic gonadotropin
same hormone family as TSH, FSH, and LH
mutation in TSH receptor may make it sensitive to hCG, and this would increase thyroid hormone during the first 10 weeks of pregnancy
3-beta-hydroxysteroid dehydrogenase
fetal adrenal cortex lacks this enzyme and therefore synthesizes mostly DHEA
Thyrotoxic crisis
occurs most commonly in patients with untreated Graves' in the presence of stress or trauma
Methimazole, propothiouracil
side effect: aplastic anemia, agranulocytosis
MEN 1
commonly presents with angiofibromas and lipomas
Diazoxide
opens ATP-sensitive potassium channels, leading to hyperpolarization of the islet cells and inhibiting insulin release
useful in insulinomas
Hashimoto's thyroiditis
increased risk of non-Hodkin B-cell lymphoma
Familial hypocalciuric hypercalcemia (FHH)
mutation in calcium-sensing receptor gene (CaSR)
Normalizing serum glucose in diabetics
acutely -> epinephrine, chronically -> cortisol
glucagon response in diabetics is not seen for some reason
Kimmelstiel-Wilson nodule
ovoid, hyaline, PAS-positive structures found in mesangial core of glomerulus
seen in diabetics
soild balls of neoplastic follicular cells in thyroid
characteristic of papillary carcinoma
associated with history of radiation to the neck
finasteride
inhibits 5-alpha-reductase
used to treat BPH
Necrolytic migratory erythema (NME)
classic symptom observed in glucagonoma
erythematous blisters and swelling at areas of greater friction
Aldosterone deficiency
salt wasting in excess of water wasting
Infantile hypothyroidism
neonatal thyroxine levels may be normal because of maternal-fetal thyroxine transfer
Alpha-2 receptor agonists (clonidine)
directly inhibit pancreatic insulin secretion
glucagon
rapidly raises blood glucose levels and leads to stimulation of insulin levels
iodine staining intraepithelial inclusion bodies
clamydia trachomatis
most common bacterial cause of sexual trasnmitted disease, leads to PID
Pudendal nerve
innervates the perineum, wraps around the ischial spine
palpation of the ischial spine allows the physician to locate the pudendal nerve
Most common cause of spontaneous abortion
chromosomal abnormalities
usually the fetus is lost in the 1st trimester
Ectopic pregnancy
most commonly due to delayed transport of the blastocyst
Testicular torsion
twisting and torsion of the spermatic cord w/ occlusion of the testicular artery and vein
Tzanck smear
test for HSV by touching slide to opened vesicle and look for multinucleated giant cells
vaginitis w/ frothy yellow discharge
trichomonas vaginalis
Struma ovarii
unilateral ovarian mass w/ symptoms of hyperthyroidism
Schiller-duval bodies
pathognomonic for yol sac (endodermal sinus tumor), resemble glomeruli
Meigs' syndrome
ovarian fibroma, ascites, pleural effusion/hydrothorax
Walthard's rests
islands of bladder-like transitional epithelium within fibrous stroma
seen in Brenner tumor of the ovary
Progestin challenge
will cause menstrual bleeding and confirm anovulation in a patient
PID
chalmydia is the most common cause, leading to type IV hypersensitivity response in the fallopian tubes that may result in infertility
human placental lactogen (hPL)
secreted by syncytiotrophoblasts; concentration rises throughout pregnancy and is proportional to fetal mass
anti-insulin activity
Levonorgestrel
high dose progesterone that disrupts endometrium and prevents implantation
Bitot's spots
buildup o fkeratin debris in conjunctiva
Neimann-Pick disease type A
CNS involvement
compared to type B, where there is no CNS involvement
Infantile cirrhosis + hypotonia
Anderson's disease (type IV glycogen storage disease)
deficiency in alpha 4,6-glucosidase (glycogen branching enzyme)
Oral hairy leukoplakia
EBV infection in HIV patients
nontender, adherent whitish lesion on tongue or oral mucosa due to hyperproliferation of lingual epithelial cells
Lateral cervical cyst
derived from second pharyngeal cleft that didn't obliterate
Narcolepsy
hypnopompic hallucinations, sleep paralysis, cataplexy, sleep attacks
Spe-A, Spe-B, Spe-C
involved in scarlet fever, transmitted via lysogenic converesion
lysogenic conversion: DNA of a temperate phage is inserted into bacterial chromosome and expressed
Confidence interval
Sample mean +/- Z * [SD/sqrt(n)]
Lymphocyte common antigen (LCA)
used to determine if there is a lymphoma
DNA footprinting
detect specific protein binding to DNA molecules by comparing fragmentation patterns of DNA w/ protein bound vs. protein unbound
Decidua basalis
composed of endometrium between the chorionic villi and the myometrium
derived from the mother
Fluoroquinolones
resistance to the topoisomerase inhibitor encoded on the chromosome
resistance via efflux pumps is encoded on plasmids
Enzyme assays
use amount of enzyme at Vmax so that the results are dependent on the amount of substrate
myofibroblasts
specialized subset of fibroblasts that express contractile proteins (actin and myosin)
principal mediators of wound contraction, which results in aesthetic and functional deficits
Down's syndrome due to mosaicism
mosaic Down syndrome patients have IQ scores that are 10-30 points higher than individuals with classic Down syndrome
Multi-drug resistance
transposons
direct inguinal hernia
passes medial to inferior epigastric artery
Her-2/Neu
receptor w/ intrinsic tyrosine kinase activity
Anticholinergic agents
anti-SLUDG properties: salivation, lacrimation, urination, defecation, gastrointestinal slowing
Second generation anti-histamines
few anticholingergic side effects
Struma ovarii
monodermal teratoma
Bowen disease
penile carcinoma in situ, solitary-whitish plaque that doesn't invade the basement membrane
Vaginal candidiasis
diagnosed by performing the germ-tube test (inoculation of a sample into animal serum)
Arthroconidia
diagnostic of dermatophytes
Hyphae w/ rosettes of microconidia
sporothrix schenckii
macroconidia
histoplasma cpasulatum
Septic arthritis in otherwise healthy, sexually active adults
N. gonorrhea
Focal fat necrosis of breast
multinucleated giant cell reaction, frequently due to trauma
parvovirus
exposure to pregnant women in first trimester may result in a fetus with aplastic anemia which leads to non-immune hydrops fetalis
Syphilis tests
VDRL to rule out, FTA-ABS to rule in
microhemagglutination test
treponeme-specific serologic test
Batson venous plexus
hematogenous spread of prostate cancer to vertebrae and pelvic bone
Kallmann's syndrome
autosomal dominant, maldevelopment of olfactory bulbs and GnRH-producing cells
Paget's disease
mucin is periodic acid-schiff (PAS) positive
Rokitansky-Kuster Hauser (RKH) syndrome
absence of upper vagina and uterus
Arias-stella phenomenon
exaggerated secretory phase during pregnancy
Endometritis
chronic due to IUD = actinomyces
Rectal pouch of douglas
site for collection of blood, malignant cells, pus, endometrial implants
Stromal hyperthecosis
bilateral ovarian enlargement, vacuolated stromal hilar cells that synthesize excess androgens, leading to hirsutism
Ritter's disease
staphylococcal scalded skin syndrome in newborns
Acanthosis nigricans
hyperplasia of stratum spinosum
Marjolin ulcer
SCC that arises from non-healing ulcer, burn wound, or osteomyelitis
Follicle that contains a primary oocyte surrounded by a single layer of flattened follicular cells
primitive and primordial follicles
oocyte surrounded by one or several cuboidal follicular cells
primary follicles
follicle that extends through the entire cortex and bulges at the ovarian surface
graafian follicle
Secondary follicle
oocyte surrounded by several layers of follicular cells and a small antrum (antrum is due to several spaces of the follicular mass fusing together)
Preeclampsia
cerebral hemorrhage and ARDS are most common causes of death
CA-125
tumor marker for papillary cystadenocarcinoma and other tumor types
Premature menopause
reduced inhibin levels, which may lead to increased FSH levels
Verrucous lesion of vulva w/ tree-like proliferation of epithelium and fibrous stroma
HPV
hGH (growth hormone)
produced by the placenta during pregnancy
Testicular tumor w/ fibrous septa containing numerous lymphocytes
seminoma
Sertoli-only syndrome
only sertoli cells are present (germinal cell aplasia), spermatogenesis is absent
ulcerative genital lesion w/ pain and inguinal lymphadenopathy
Haemophilus ducreyi: gram-negative, pleomorphic rod w/ characteristic "school of fish" pattern on gram-stain
Granuloma inguinale
Klebsiella granulomatis
Dysfunctional uterine bleeding
most commonly due to anovulatory cycles
Chlamydia trachomatis
unable to make ATP
Intraductal papilloma
benign, neoplastic tumors typically located near the nipple under the areola
Endometrium w/ long, narrow, coiled glands lined by a single layer of columnar epithelium showing regular, uniform, small nuclei, and apical secretory vesicles
secretory epithelium
Choriocarcinoma
likes to go to the lungs
Radical mastectomy
remove underlying tumor, axillary lymph nodes, some pectoralis
18-alpha hydroxylase
aldosterone synthase
Progression of high grade cervical dysplasia
60% presist at the same level of dysplasia
N. gonorrhoea
pili is the most important mechanism of pathogenesis; promotes adherence to mucosa and protection from phagocytosis, also antigenic variation
acute epididymitis and orchitis
N. gonorrhoea and C. trachomatis
Chronic endometritis
inflammatory infiltrate of lymphocytes, plasma cells, histiocytes
HPV
mechanism of pathogenesis similar to retinoblastoma and osteosarcoma
Breast cancer metastasis to bone
unusual in that it causes both lytic and blastic lesions
Neonatal pneumonia preceeded by conjunctivitis
Chlamydia
may present with a staccato cough, CXR w/ scattered infiltrates and hyperinflation of lungs
Congenital lipoid adrenal hyperplasia
mutation in steroidogenic acute regulatory protein (StAR): protein necessary for transport of cholesterol from the outer to inner mitochondrial membrane in adrenals and gonad
deficiency in all steroid hormones (C21, C17, C18), absent response to ACTH and hCG, large, lipid-laden adrenals
mixed testicular tumor
male testicular tumor composed of multiple types of various tumors
HTN and proteinuria before 20 weeks gestation
hydatidiform mole
Vagina swab of prepubertal girls and postmenopausal women
Staphlyococcus epidermidis
Acute bacterial prostatitis
E. coli (over 35 years old)
Dinoprostone
prostaglandin E2
induces cervical softening and effacement, cervix to dilate, uterus to contract, helps induce labor
Orchitis w/ obliterative endarteritis
syphilis
Bartholin's gland cyst
obstruction, usually a sequela of a previous infection, leading to pain and swelling of the posterolateral part of the labia majora
Chronic ACL injuries
involve damage to medial meniscus (not lateral like acute ACL injuries)
Triad junction
consists of the T-tubule, the sarcoplasmic reticulum, and the 15 nm space between them
anterior shoulder dislocation
externally rotated and abducted
posterior shoulder dislocation
internally rotated and adducted
I band
most common site for muscle strains because it consists only of actin filaments
Trendelenburg sign
abnormal gait caused by weakness of abductor muscles of lower extremities due to lesion of the superior gluteal nerve
osteoid
newly formed bone matrix
Carbonic anhydrase II deficiency
autosomal recessive, triad of osteoporosis, renal tubular acidosis, and cerebral calcifications
CA II: generates carbonic acid from water and carbon dioxide
McCune-Albright syndrome
4 Ps: polyostotic fibrous dysplasia, pigmented skin lesions, precocious puberty
caused by non-inherited postzygotic activating mutation of Gs subunit leading to constitutive activity; example of genetic mosaicism
Gardner syndrome
autosomal dominant variant of FAP w/ osteomas, desmoid tumors, dental abnormalities, congenital hypertrophy of retinal pigmented epithelium, skin tumors, and extracolonic cancers (thyroid, hepatobiliary, CNS)
Ollier's syndrome
multiple enchondromas w/ 10-25% chance of malignant transformation to chondrosarcoma
Maffucci's syndrome
multiple enchondromas and soft tissue hemangiomas w/ 100% chance of malignant transformation to chondrosarcoma
Complications of osteomyelitis
sequestrum: areas of bone necrosis due to acute inflammation -> involucrum: new bone growth that forms a sheath around dead bone
Legg-calve-perthes disease
aseptic necrosis of femoral head ossification center, possibly due to problems w/ the medial femoral circumflex artery (main supply to the head of the femur)
clinical picture: limp to avoid pain (pain is usually in the anterior thigh) or painless limp, irregular appearance of the capital femoral epiphysis on xray,
osteochondritis dessicans
trauma to articular epiphysis -> ischmeia -> aseptic necrosis and failure of articular epiphyses
pannus
granulation tissue rich in inflammatory cells and fibroblasts that proliferates and releases cytokines -> destruction of articular cartilage w/ reactive fibrosis and eventual akylosis
RA treatment
First line: NSAIDS, DMARDs (disease-modifying antirheumatic drugs) such as sulfasalazine, hydroxychloroqiune, MTX
Second line: TNF-alpha inhibitors, Leflunomide (inhibits pyrimidine synthesis), Rituximab (anti-CD20 antibody binds CD20 on surface of B-cells leading to their destruction)
Felty's syndrome
RA + splenomegaly + leukopenia
Caplan syndrome
RA + intrapulmonary rheumatoid nodules + pneumoconiosis
Popliteal (Baker's) Cyst
increased intra-articular pressure -> outpouching of snovial sack posterior to knee
Congenital 3rd degree heart block
SS-A and SS-B antibodies can cross placenta and target AV node, leading to destruction
Ankylosing spondylitis extra-articular manifestations
anterior uveitis (monocular pain, photophobia, blurry vision), aortitis/aortic regurgitation, cardiac conduction defects (3rd degree block), involvement of thoracic spine -> decreased chest expansion -> restrictive pattern on PFTs
Reiter sndrome
classic triad (conjunctivitis, urethritis, arthritis)
also oral ulcers, keratoderma blenorrhagica (erythematous scaly hyperkeratotic skin lesions on palms and soles), circinate balanitis (red scaly area on glans penis w/ gray serpiginous annular edge that spreads outwards in phases
Drug induced lupus
Q CHIMPP: quinidine, chlorpromazine, hydralazine, isoniazid, methyldopa, penicillamine, procainamide
anti-histone antibodies
Chronic infectious arthritis
TB, Lyme disease
Myasthenia gravis
follicular B-cell hyperplasia in thymus, thymoma
Lambert-Eaton syndrome
small cell lung carcinoma
Dermatomyositis
antibody-mediated damage to blood vessels surrounding muscle fascicles -> perfascicular inflammation and atrophy
Sarcoidosis
lung (pulmonary fibrosis), skin (erythema nodosum w/ Schaumann and asteroid bodies), Eyes (anterior uveitis)
epithelioid histiocytes needed on biopsy for diagnosis; asteroid bodies and giant cells are also seen, but not required
Linoleic acid
precursor for arachadonic acid and essential fatty acid needed in diet
recurrent miscarriages in the first trimester
chromosomal abnormalities (robertsonian translocation)
Congenital CMV
heptaosplenomegaly, periventricular brain calcification, petechial hemorrhage (blueberry muffin rash),
Familial gonadotropin-independent premature Leydig cell maturation
mutation in the LH receptor causes it to be constitutively active
elevated testosterone, suppressed gonadotropin levels, Leydig cell hyperplasia, seminiferous tubule dysgenesis
Barr body
inactivation of X chromosome
seen in Klinefelters as well as in normal females
LH receptors on Granulosa cells
as follicle approaches ovulation, LH receptors begin to be expressed by granulosa cells, probably as a response to increased estrogen and FSH
Congenital syphilis
saddle nose, Hutchinson's teeth, mulberry molars, saber shins, interstitial keratitis, deafness
treat w/ penicillin
Café-au-lait spots
due to peripheral nerve tumors that induce hyperpigmentation of overlying skin
seen in tuberous sclerosis
Gonococcal arthritis
petechial rash, tenosynovitis, involvement of ankles and knees
fibrillin
component of elastin-associated microfibrils
abnormal in Marfan
HLA-B27
seronegative spondyloarthropathies, acute anterior uveitis
Malignant otitis externa
caused by P. aeruginosa, may spread to mastoid bone, temporal bone, sinuses, meninges, and brain
pseudomonas associated w/ ecthyma gangrenosum
Familial pulmonary hypertension
inactivating mutation in BMPR2 gene
BMPR2 gene normally functions to inhibit vascular smooth muscle proliferation
Solubility of oxygen in blood
inversely related to temperature (increase in temperature = decrease in O2 solubility)
oxygen content in blood = (Hb*1.34*%sat) + (0.0031*PaO2)
Charcot-Leyden crystals
hexagonal, double-pointed, needle-like crystals in bronchial secretions in asthmatic patients
Curschmann's spirals
desquamated epithelium casts in sputum seen in asthmatic patients
can lead to whorled mucous plugs
osteopetrosis
genetic disease characterized by reduced osteoclast activity resulting in diffuse symmetric skeletal sclerosis
leads to pancytopenia due to domnation of the marrow
Mosaic pattern of newly formed woven bone
paget's disease
increased risk of osteosarcoma
Steroid myopathy
caused by exogenous corticosteroid use or Cushing disease
can lead to insidious onset of muscle weakness of the proximal muscles w/ preferential atrophy of type II fibers
Inclusion body myositis
usually involves both distal and proximal muscles
inclusion bodies seen on biopsy (large rimmed vacuoles in muscle fibers)
Cleidocranial dysostosis
absence of part of the clavicles w/ broad skull, facial and dental anomalies
disorder of intramembranous ossification bones
Clubbing of nails
associated w/ lung cancer, mesothelioma, bronchiectasis, congenital cyanotic heart disease, hepatic cirrhosis
in these conditions, the clubbing is accompanied by formation of new subperiosteal bone (hypertrophic osteoarthropathy)
Energy use during exercise
0-10 seconds: stored ATP, creatine phosphate; 10-100 seconds: glycogen;
Basic calcium phosphate
seen in apatite-associated arthropathy
produces spherical clumps of nonbirefringent submicroscopic crystals
Gout
possibly abnormality in purine salvage pathway
bacillus anthracis
boxcar-shaped, gram positive rod
extension of thumb
radial nerve only
innervates extensor pollicus brevis and longus
Long-term glucocorticoid use
hypocalcemia (decreased Ca2+ uptake in the gut)
Crutches
damage to radial nerve
Median nerve
only nerve that traverses the carpal tunnel
Still's disease
seen in Juvenile rheumatoid arthritis (JRA)
fever, rash, polyarthritis
Juvenile rheumatoid arthritis
polyarticular JRA: disabling arthritis predominates
Pauciarticular JRA: arthritis limited to a few joints, uveitis w/ portential for blindness
Lead poisoning
associated w/ gout due to interstitial nephritis that leads to decreased excretion
myotonic dystrophy
most common adult muscular dystrophy, selective atrophy of type I fibers
autosomal dominant CTG repeat -> facial muscle weakness, sustained grip, frontal balding, cataracts, cardiac involvement (conduction defects)
Dupuytren's contracture
fibromatosis involving palmar fascia leads to contraction of single or multiple fingers
associated w/ alcoholism
Desmoid tumor
fibromatosis of anterior abdominal wall in women
associated w/ previous trauma and Gardner's polyposis syndrome
periosteum
torn during fracture -> supplies osteoblasts to produce new bone that reunites the two ends
can lead to hetertopic ossification (bone formed outside the regular bone)
Fracture of neck of fibula
damage to peroneal nerve
Erythema multiforme
erythematous patches w/ pale, vesicular, or eroded centers (target lesions) due to immune complex deposition in dermal blood vessels
causes: certain infections (HSV, enteroviruses, mycoplasma), drugs, neoplasia, foods; pathogenesis related to HSV involves triggering CD8+ cytotoxic cells -> apoptosis of some keratinocytes
Rubella
fine rash that begins at hairline and spreads down to torso in a child that is not very ill
also see cervical lymphadenopathy, NO KOPLIK
Avulsion of lesser trocanter
due to sudden strain of muscle that leads to reflex contraction that breaks the bone
psoas major inserts at the lesser trochanter
Schaumann and asteroid bodies
sarcoidosis
lupus pernio (rash on nose and cheeks) is also seen
Coal miner's pneumoconiosis
simple CWP: scattered coal macules in upper lobe
complicated CWP: requires years to develop, progression from simple CWP, lesions throughout lungs
Anthracosis
benign accumulation of coal dust found in urban dwellers
Therapeutic supplemental O2 in NRDS
retinopathy of prematurity and bronchopulmonary dysplasia
recurrent idiopathic pleural effusions
mesothelioma presentation
surfactant synthesis
increased cortisol, prolactin, thyroxine
decreased insulin
Long-thoracic nerve
innervates the serratus anterior
pearly papules
basal cell carcinoma
palisading of basal cell-like nuclei at edge of clusters of cells penetrating into the dermis
genioglossus muscle
protrude the tongue
hypoglossus muscle
retract the tongue
palatoglossus muscle
retract tongue and upward towards the palate
scaphoid fracture
pain in the anatomic snuffbox after a fall on outstretched hands is pathognomonic
Axillary sheath
contains the axillary artery, 3 cords of the brachial plexus and is found in the axilla
anterior displacement of humerus
damage to axillary nerve
basophilic rhomboid crystals
calcium pyrophosphate crystals
seen in pseudogout, radiographically dense, unlike the crystals of gouty arthritis
Pulmonary embolism
presents with the combination of respiratory alkalosis and hypoxemia
V/Q scan shows decreasd perfusion with areas of normal ventilation
Rubella
fine rash that begins at hairline and spreads down to torso in a child that is not very ill
also see cervical lymphadenopathy, NO KOPLIK
Hampton's hump
wedge shaped area of infarcted tissue seen in PE
Methenamine silver stain
Pneumocystis jiroveci
Owl eye inclusions in immunocompromised/immunosuppressed individual
CMV
Emphysema
loss of elastic recoil -> decreased FEV1, increased residual volume, increased TLC
Old age lungs
decreased elastic recoil and increased distensibility (compliance) of the lungs
Aspiration of food
leads to V/Q mismatch
bacterial abscess
results from bronchial obstruction or aspiration of oropharyngeal contents (especially in those predisposed to loss of consciousness)
Forscheimer spots
red spots on soft and hard palate, seen in Rubella
Body, head, or pubic louse
treat w/ permethrin
Leser-trelat
rapid increase in number of sborrheic keratosis
phenotypic marker for stomach adenocarcinoma
Ichthyosis vulgaris
most common inherited skin disorder (AD) w/ inreased thickness of stratum corneum
Munro microabscesses
neutrophil collections in stratum corneum seen in Psoriasis
terbinafine
treat onychomycosis
RA biopsy
proliferative synovitis w/ many lymphocytes, macrophages, and plasma cells because it is a chronic process
subcutaneous nodules seen in RA are areas of fibrinoid necrosis surrounded by palisading epitheliod cells
Muscle tension
passive tension (preload) increases as the muscle is stretched beyond it's resting length
total tension is passive tension + active tension. Active tension cannot be measured so must therefore be estimated using total tension - passive tension
Re-epithelialization
ingrowth of epidermal cells from underlying skin appendages such as hair follicles and sweat glands of the dermis
Pseudo-horn cysts
seborrheic keratosis
Short saphenous vein and lymph drainage
drains lateral side of dorsum of foot and runs on the posterior side to drain in to the popliteal lymph nodes
Long saphenous vein and lymph drainage
drains and runs on the medial side of the leg and drains into inguinal lymph nodes
Splay
glucosuria when seurm glucose is above 180 but below 350, and the transporters aren't quite saturated
due to nephron heterogeneity and low affinity of the Na-Glu transporters
Aliskerin
blocks renin activity
Posterior dislocation of the clavicle
impingement onto the trachea
Gluteus medius/superior gluteal nerve
trendelenberg sign: stand on 1 leg and contralateral hip drops
Most common lung cancer
bronchogenic adenocarcinoma
even though it's the most common in non-smokers, it's also the most common in smokers
Oral candidiasis
nystatin "swish and swallow"
Succinylcholine
depolarizing skeletal muscle relaxant; prolonged use may lead to release of substantial amounts of K+ -> hyperkalemia and arrythmias
Erb's palsy
due to defect in C5, C6 (musculocutaneous nerve) -> problem w/ biceps brachii
Protein/serum ratio > 0.5
exudate
Reiter's syndrome
Ureaplasma, Campylobacter, Chalmydia, Shigella, Salmonella, Yersinia
Resistance in pseudomonas
mutation of a porin protein
Treatment of cutaneous burns
silver sulfadiazine or mafenide (if they have sulfa allergy)
cidal for gram negative, gram positive bacteria, as well as fungi
Fusobacterium
anaerobe seen in lung abscesses
anaerobes like bacteroides, fusobacteirum, and peptococcus are all found in the oral cavity
lung cancer specifically associated w/ lung scarring and old granulomatous disease
adenocarcinoma
found peripherally
BPH
most common cause of postrenal azotemia
calsequestrin
binds Ca2+ after depolarization and as the muscle relaxes
Mannitol salt agar
Staph aureus can ferment mannitol, turning it yellow
MPGN type I
associated w/ secondary causes of MPGN such as HBV, HCV, syphilis, malaria
Goodpasture syndrome
renal crescentic glomerulonephritis + pulmonary involvement
anti-GBM antibodies can cross-react w/ pulmonary alveolar basement membranes
Alport syndrome
triad: hereditary nephritis, sensorineural deafness, ocular abnormalities
due to defect in collagen IV
WAGR complex
Wilms' tumor, Aniridia, Genitourinary malformation, mental-motor Retardation
Wilms': due to deletion of WT1 and WT2 on chromosome 11; Aniridia: due to deletion of PAX6 on chromosome 11
blunting of calyces
Chronic pyelonephritis due to chronic vesicoureteral reflux
Dent's disease
x-linked recessive condition of proximal tubule
leads to hypercalciuria and calcium kidney stones
Max velocity of shortening of muscle
due to rate of ccling of crossbridge attachments, which is basically hydrolysis of ATP (dependent on myosin ATPase)
Chylous effusion
unusual milky-white fluid that separates into a thin white layer (cells) and thicker clear layer (triglycerides)
Step pneumoniae pneumonia treatment
azithromycin
P-pili of E. coli
play a role in pathogenesis of UTIs
Ciprofloxacin
cytochrome inhibitor
used to treat H. influenza
Diuretics and creatinine clearance
loop diuretics are effective down to a GFR of 10
thiazide and potassium-sparing diuretics are effective only down to 40
Dialysis cysts
small shrunken kidneys with large cysts
nitrate test
most Enterobacteriaceae (gram-negative enteric rods) are able to form nitrite from nitrate
thus, this test is used to determine if a UTI is caused by enterobacteriaceae
Expiratory flow rate
the "effort-independent" portion of the curve is because the airways are collapsing and the patient can't blow air out any quicker
Pickwickian syndrome
morbidly obese individual w/ fatty neck causes intermittent airway obstruction that leads to acute respiratory acidosis
reduced O2, increase CO2, reduced pH, modestly increased bicarb
oxybutynin
antispasmodic effect on smooth muscle and inhibits the ACh action
treatment of urinary incontinence
Plasmacytoma
mass found in bone or oronasopharynx (involving soft tissue)
associated w/ a mild M-spike of IgG, may eventuall develop into multiple myeloma after 10-20 years
Lung abscess
MCC staph aureus, anaerobes
Mycoplasma pneumonia tx
Erythromycin
Reserpine
inhibits VMAT
allows degradation of dopamine by MOA
AA amyloid in glomerulus
tuberculosis and other chronic antigenic inflammatory diseases
Corticosteroid effect on bone
increase osteoclastic function as well as inhibit osteoblastic function
Bartter's syndrome
decreased NaCl transport in the ascending loop of Henle and early distal tubule
leads to hypochloremic, hypokalemic, hypercalciuric, hypotensive metabolic alkalosis. Resultant increase in ATII levels leads to ATII insensitivity of the vascular smooth muscle
Auramine-rhodamine stain
indicates mycobacterium tuberculosis
Nitrofurantoin
damages bacterial DNA
used for recurrent UTIs, side effects include pulmonary fibrosis and G6PD hemolytic anemia
Vulvovaginal candidiasis tx
miconazole, clotrimazole
Crush injury
leads to release of K+ from muscle and hyperkalemia
Peripheral chemoreceptors
respond first, before central chemoreceptors, to changes in PaCO2
Collagen IV
found in basement membrane, as well as the lens of the eye
ACE inhibitors
decreased GFR and further exacerbate acute renal failure
Cyclosporine
nephrotoxicity -> increased BUN and creatinine
Klebsiella pneumonia tx
third generation cephalosporin (cefotaxime, ceftriaxone, ceftazidime)
Acetazolamide
only diuretic that acts upstream of the macula densa -> increases NaCl in the rest of the tubules
results in the macula densa sensing more NaCl, which leads to constriction of the afferent arteriole
Acute salicylate poisoning
cause acute respiratory alkalosis and eventual metabolic acidosis
Acute salicylate poisoning
cause acute respiratory alkalosis and eventual metabolic acidosis
Lysogenic phase in bacteria
ShigA toxin, Botulinum, Clostridium, Diphtheria, Erythrogenic exotoxins of strep
ABCDE
Cooperative play in children
begins at 4 years of age
Liquefactive necrosis
result of hydrolytic enzymes released from dying cells
Maternal estriol blood levels
best indicator of fetal well-being
significant drop in maternal estriol may indicate fetal jeopardy
LFA-1 and ICAM-1
interaction necessary for tight binding of white cells to the endothelium which allows them to leave the vessel to go to an area of injury
chronic alcohol and smoking
induce cytochrome P450
Raw oysters, contaminated seafood
Vibrio vulnificus, V. parahaemolyticus
gram (-), comma-shaped rods that are isolated on alkaline media
Type I Hypersensitivity
IL-4 is produced to stimulate production of IgE
Vibrio toxin
similar to ETEC toxin
both activate adenylate cyclase by ADP ribosylation of GTP-binding protein
Ketotifen
selective, non-competitive histamine receptor antagonist and mast cell stabilizer
Acute cholecystitis
treat w/ third generation cephalosporin
treats gram negative, gram positive, and some anaerobes
Most common gram (-) rod that infects children from maternal contamination in the birth canal
E. coli
K1 is an important capsule antigen that aids in neonatal disease
Scalene triangle syndrome (thoracic outlet syndrome)
when the lower trunk of the brachial plexus and the subclavian artery are compressed between the anterior scalene and the middle scalene
Aspirin-induced asthma
inhibition of the cyclooxygenase pathway leads to too much leukotriene and bronchial constriction
Pertussis
bordetella pertussis increases histamine sensitivity, blocks lymphocytosis, increases cAMP (leads to edema), and also increases insulin secretion (leads to hypoglycemia)
ketolorac
NSAID
Irritation of liver
results in irriration of phrenic nerve -> pain in the right upper quadrant + radiant pain to the shoulder region
Restrictive lung disease
increased elasticity, decreased compliance
Psoas abscess
spinal infection (classically tuberculosis) spreads along the psoas sheath
leads to bulge on flank and contralateral buldge on groin
tyrosine
aromatic amino acid
most common cause of death in cirrhosis
esophageal variceal rupture
pneumomediastinum in the setting of vomiting
Boerhaave syndrome
Pneumaturia
colovesical fistula, may be caused by diverticulosis
Intensely PAS-positive bacteria
Tropheryma whippelii
causes Whipple's disease: arthralgias, diarrhea, lymphadenopathy; can also have cardiac and neuro manifestations
Reyes syndrome in Kawasaki disease
children and teens w/ kawasaki who require aspirin therapy SHOULD NOT discontinue aspirin and should consider vaccination to avoid viral infection
Recurrent infections, thrombocytopenia, eczema
Wiskott-aldrich syndrome
Renal failure diet
designed to control the amount of protein and phosphorus in a patient's diet: high-carbs, moderately fatty diet, limit sodium, limit total fluid intake
Tolterodine
blockade of muscarinic ACh receptors in bladder wall is used to reduce the effect of parasympathetic hyperactivity in patients w/ spinal cord transection that have incontinence
Vasa recta
poorly oxygenated part of kidney, can become an area of sickling
Recurrent acute pyelonephritis
kidney stones
Increased arterial CO2 effect on brain
increased CO2 dilates blood vessels in the brain leading to increased flow, while decreased CO2 leads to vasoconstriction
think about it this way: hyperventilation leads to dizziness, which means that your brain is not getting enough O2 because the blood vessels are constricting because CO2 levels are low
Mycobacterium avium intracellulare treatment
clarithromycin, rifabutin, and ethambutol
CFTR
Anionic channel that is gated by ATP hydrolysis and involves regulation by protein kinase A
Vulvovaginitis
associated w/ high vaginal pH, diabetes, and use of antibiotics
Alosetron
5-HT3 antagonist used for diarrhea-predominant irritable bowel syndrome
restricted access usage in US because of serious gastrointestinal adverse effects like ischemic colitis
Kaposi sarcoma
spindle-cell neoplasm that is highly associated w/ AIDS and HHV-8
similar in appearance to angiosarcoma (proliferating stromal cells and endothelium creating vascular channels that contain blood cells)
Budd-chiari
caused by polycythemia vera, OCPs, pregnancy, HCC, chronic infections
PAS-positive stuff
alpha1-antitrypsin globules in liver, Kimmelsteil-Wilson nodules in kidney, Paget's disease of the nipple
Neonate w/ cirrhosis and E. coli sepsis
Galactosemia due to galactose-1-phosphate uridyltransferase (GALT) deficiency
hemochromatosis
classic triad: micronodular cirrhosis, Diabetes Mellitus, bronze skin pigmentation
Protozoa that infects small intestine and look crescent-shaped next to the epithelial brush border
giardia lamblia
Entamoeba histolytica
usually infects the large intestine or liver
Necrotizing enterocolitis
most common when infants are started on oral foods, especially formula fed children
present w/ distended abdomen and gangrene of the terminal ileum and ascending colon
Increased IL-10
can decrease contact dermatitis
IL-10 is produced by TH2 and inhibits TH1 (stimulate cell-mediated immunity and delayed hypersensitivity)
Prolonged antibiotics
deficiency in gut bacteria lead to vitamin K deficiency -> bleeding and blood in stools
RUQ pain + bloody diarrhea
Entamoeba histolytica
Parvovirus in adults
no slapped cheeks, instead arthralgias and arthritis
Lipoprotein lipase
located on the luminal surface of vascular endothelium of adipose tissue
MI necrotic changes on light microscopy
become evident after 4-12 hours
3 days: coag necrosis will advance and neutrophils will invade; 5-7 days: necrotic debris is removed and granulation tissue is formed
Trientine
second line agent for Wilson's disease
because 30% of patients can't handle long term penicillamine
Wilson's disease diagnosis
slit-lamp examination of the eyes demonstrates Kayser-Fleischer rings in Descemet membrane of the cornea
Gastric carcinoma
H. pylori is the strongest association, followed by smoking, then pernicious anemia, then EtOH
Menkes disease (Elhers-Danlos type IX)
depigmented, lusterless hair along w/ facial, ocular, vascular, and cerebral manifestations
due to a mutation in copper transport that leads to a defective Lysyl Oxidase enzyme, which is responsible for crosslinking collagen fibers
bifid ventral pancreatic bud
causes rotation around the duodenum distal to the ampulla of vater, which leads to obstruction
presents w/ bilious vomiting, polyhydramnios, double bubble sign
Thiazolidinediones (pioglitazone, rosiglitazone)
decreases TGs, insulin, Glucose levels, and increases HDL
Gastric heterotopia
occurs in small intestine and can produce enough acid to cause PUD
Amoebae w/ ingested erythrocytes
entamoeba histolytica
Choledocholithiasis
colicky RUQ pain
compared to cholecystitis, which is constant RUQ pain
Lactulose
given for treatment of hepatic encephalopathy
lactulose is degraded by gut bacteria, resulting in acidic pH, which shifts the equilibrium from NH3 to NH4+ and this minimizes gut absorption of ammonia
Medium-chain acyl CoA dehydrogenase (MCAD) deficiency
important in breaking down C-8, C-10 acylcarnitines after LCAD has made them.
medium chain length fatty acids accumulate, eventually spilling out of the mitochondria via the carnitine shuttle. Inability to conduct beta-oxidation results in low ATP levels (low ATP inhibits the urea cycle, leading to hyperammonemia)
Octreotide
used to treat variceal bleeding, acromegaly, diarrhea in various endocrine disordesr
Differentiating feature between anti-ACh agents and botulinum toxin
skeletal muscle weakness (seen in botulinum)
Hantavirus pulmonary syndrome
most common in four corners of the US, bunyaviridae
the virus is inhaled from aerosolized secretions from the common deer mouse, begins with nonspecific prodrome followed 4-5 days later by respiratory symptoms that progress to ARDS
Ehrlichiosis
caused by Ehrlichia phagocytophila, an intracellular bacterium transmitted by Ixodes
similar to rocky mountain spotted fever, but doesn't have a rash. Pathognomonic berry-like clusters of organisms in granulocytes
Tinkly bowel sounds
small intestinal obstruction
Prochlorperazine
phenothiazine that blocks dopamine receptors in the floor of the fourth ventricle (postrema)
used as an antiemetic
Cystic artery
found in the hepatoduodenal ligament
obstructive sleep apnea syndrome
hypoxemia w/ hypercapnia
Gastroschisis
caused by incomplete fusion of the lateral body folds
as opposed to failure of the intestinal loop to retract from the umbilical cord, which is seen in omphalocele
Conjunctivitis caused by gram negative pleiomorphic rods
H. influenzae
culture on chocolate agar w/ X and V or co-culture w/ S. aureus
RhD-positive attack on newborn
type II hypersensitivity
Superior vena cava syndrome
usually due to small cell carcinoma
Roth's spots
small white spots surrounded by hemorrhage bilaterally on the retina
Goodpasture syndrome is most similar to bullous pemphigoid
these are both cytotoxic type II hypersensitivity
Graves' disease, on the other hand, is type II, but it's noncytotoxic
GI hormones w/ trophic properties
Gastrin (intestinal mucosal growth), CCK (pancreatic growth), and secretin (pancreatic growth)
Cyclophosphamide
coadminister w/ mesna to prevent hemorrhagic cystitis
Celiac sprue
limited to the proximal small bowel (jejunum mostly)
Salicylate poisoning
made worse by things that acidify the urine, like NH4Cl
treated w/ bicarb to alkalinize the urine
Aprepitant
NK1 antagonist (blocks the action of human substance P) used to treat nausea and vomiting in patients who are on chemo
Dumping syndrome
occurs after gastric bypass surgery because food is being delivered to small intestine too quickly
instruct to eat smaller meals with less carbs, high protien, and more fats, because fats are absorbed more slowly and lead to less contraction by the small intestine, which helps improve the diarrhea symptoms of dumping syndrome
Slaughterhouse workers, veterinarians, and farmers
Brucellosis
undulating fever, lymphadenopathy, hepatosplenomegaly
Vibrio vulnificus
after eating raw shelfish -> septicemia, fever, chills, hypotension, fluid-filled blisters that progress to muscle necrosis of the lower limbs
gastroenteritis + cellulitis
Vinyl chloride
angiosarcoma of liver
seen in rubber industry
Ursodiol (ursodeoxycholic acid)
primary bile acid that acts by reducing cholesterol synthesis and secretion into bile and is effective in dissolving small cholesterol gallstones in some patients
Gastrinoma
proliferation of parietal cells in the body of the stomach due to increased gastrin levels (trophic effect)
Neonatal CMV vs toxo
CMV has periventricular calcifications, while toxo has calcifications distributed throughout the cortex and basal ganglia
hCG lacks MHC antigens
this is why it doesn't evoke and immune response
heterogenous complex of diseases w/ onset of recurrent bacterial infections secondary to markedly decreased antibody levels that becomes evident in 2nd or 3rd decade of life
Common variable immunodeficiency (CVID)
patients can have intact cell-mediated immunity or deficient t-cell mediate immunity
Drugs that cause SIADH
antidepressants (TCAs, SSRIs, MAOIs), antipsychotics, carbamazepine, antineoplastics
Coxsackie virus A infection of neonates
involvement of heart, liver, and brain that resolves without sequelae
CMV causes similar disease, except it has major sequelae
Rocky Mountain spotted fever
intracellular infection of endothelial cells
finger-clubbing, hypertrophy pulmonary osteoarthropathy
associated w/ bronchogenic carcinoma, benign mesothelioma, and diaphragmatic neurilemmoma
Tularemia
found in missouri, arkansas, oklahoma
ulcerative form is the most common, but there is also a pneumonic form that shows granulomas and stuff
risk for becoming oral malignancy
leukoplakia
Hartnup disease
defect in amino acid transport in renal and intestinal epithelium
see free amino acids in urine and symptoms similar to pellagra, except that there is a normal amount of niacin (tryptophan is a precursor of niacin)
types of stains
sudan stain (fat), Ziehl-Neelsen (aka acid-fast), reticulin (cirrhosis/fibrosis), Prussian blue (iron)
X-linked immunodeficiency disorders
Bruton, Wiskott-Aldrich, and some SCID
docusate sodium
stool softener
microvilli
contain actin and myosin filaments
microsomal transfer protein
essential for packaging of hepatic TGs and other components to be secreted as chylomicrons
deficiency leads to low chylomicrons, VLDL, LDL, as well as deficiency of fat-soluble vitamins
HNPCC
microsatellite instability is a characteristic of mutations in this gene (MLH1 gene)
pigment stones in gallbladder
associated w/ clonorchis sinensis
Kernicterus
unconjugated bilirubin deposition in basal ganglia
Pregnant mother takes sulfa drugs in 3rd trimester
results in kernicterus of the newborn
tripolar mitosis
abnormal mitotic spindle
Campylobacter jejuni
grows at 42 C
liposarcoma
pleomorphic lipocytes that resemble embryonal lipoblasts. Cytoplasm of cells is filled w/ lipid vacuoles that indent the nuclear membrane
Full blown AIDS related infections
HIV encephalopathy, PCP, Kaposi, cryptosporidiosis, Myco avium intracellulare
Cryptosporidium mechanism
intracellular multiplication in brush border and lysis of cells leading to severe watery diarrhea
this is as opposed to Entamoeba and Shigella, which invade the submucosa and cause dysentery
Compensatory response in COPD
increased renal ammonium secretion
Ulcerative colitis
increased risk of seeing another IBD (Crohn) in the family
Megestrol acetate
increases apetite in patients on antineoplastic drugs
Gastrin location
found mostly in antrum of stomach, but also in the jejunum and duodenum
Telomerase
a reverse transcriptase that is inhibited by NNRTIs and NRTIs in patients w/ HIV
Most common cause of trisomy induced abortion
trisomy 16
cytoplasmic blebbing
indicates apoptosis
cysts with 4 nuclei
Entamoeba histolytica
Theophylline
causes seizures
used in acute asthma management
Secretin stimulation test
used for Zollinger ellison, because it inhibits antral gastrin secretion, but stimulates pancreatic gastrin secretion
Valproic acid
assoicated w/ thrombocytopenia
GIP
only GI hormone released by fats, proteins, AND carbs
secretin (fat), CCK (fat and protein), gastrin (protein), motilin (fat)
Mixed acidosis
cardiopulmonary arrest
leads to a high arterial carbon dioxide due to respiratory standstill and metabolic acidosis due to lactic acidosis
Glassy intranuclear eosiniphilic inclusions and punch out lesions in esophagus
HSV, most commonly in immunocompromised
Erythrogenic malarial infection is cleared by what immune cell
NK cell b/c RBCs don't have MHC
Pancreatic pseudocyst rupture
the pseudocyst is filled w/ pancreatic enzymes and lysed blood and rupture may trigger severe gastrointestinal hemorrhage
Panic attack
assoicated w/ hypertension and peptic ulcer disease
Metformin
side effect: lactic acidosis
Meclizine
H1 receptor antagonist that's considered an antiemetic