Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
116 Cards in this Set
- Front
- Back
What UTI causing bacterium is associated with struvite stones?
|
proteus mirabilis
|
|
Chlamydial infections (PID) can have these 2 syndromes as a complication
|
Reiter's
Fitz-Hugh-Curtis syndrome- infection of the liver capsule and violin string adhesions of parietal peritoneum to liver |
|
Name the syndrome and etiology: infection of the liver capsule and violin string adhesions of parietal peritoneum to liver
|
Fitz-Hugh-Curtis
|
|
What is the sign name when checking for cervical motion tenderness?
|
Chandelier sign
|
|
Nosocomial infection associated with hyperalimentation?
|
Candida albicans
|
|
Name 2 bacteria responsible for nosocomial urinary cath infections?
|
E.coli
Proteus Mirabilis |
|
PCP in Aids starts at what count?
|
<200 CD4
|
|
Osteomyelitis in most people is caused by S. aureus, but in pts with sickle cell anemia it is often what bacterium?
|
Salmonella
|
|
Triad of toxo gondii in infants
|
choreoretinitis, hydrocephalus, intracranial calcifications
|
|
Branching rods in oral infection?
|
Actinomyces Israelii
|
|
What test is positive during Lymphogranuloma venereum
|
Frei test
Chlamydia trachomatis (LK) |
|
When superantigens bind to MHCII outside the antigen pocket and stimulate polyclonal T cells, what 2 major cytokines are mass released?
|
Gamma-interferon
Il-2 |
|
Scarlet fever is caused by?
|
Strep Pyogenes
Group B |
|
Urease positive bugs
|
Klebsiella
H. Pylori Ureaplasma Proteus (struvite stones Hello?!) |
|
Obligate anaerobes
|
Clostridium
Actinomyces Bacterioides ABC mnemonic |
|
Obligate Aerobes
|
Nagging pests must breathe
Nocardia Pseudomonas Mycobacterium tb Bacillus |
|
Group A Strep
|
beta hemolytic
strep pyogenes |
|
Clostridium has which exotoxin?
|
exotoxin a, which is a lecithinase, breaks down tissues
|
|
Gram positive rods that are filamentous, branched?
|
Nocardia- sulfa- soil
Actinomyces-anaerobe, sulfur granules, penicilin drugs SNAP mnemonic for tx |
|
a test performed to confirm a diagnosis of lymphogranuloma venereum. Killed antigen, originally derived from infected patients, is injected intradermally in one forearm, and a control material is injected into the other arm. If a red, thickened papule develops at the site of injection of antigen, the test result is positive. See also Chlamydia./ Lymphogranuloma venereum
|
Frei test
|
|
Frei Test
|
a test performed to confirm a diagnosis of lymphogranuloma venereum. Killed antigen, originally derived from infected patients, is injected intradermally in one forearm, and a control material is injected into the other arm. If a red, thickened papule develops at the site of injection of antigen, the test result is positive. See also Chlamydia./ LGV
|
|
What ricketsia will not give a positive Weil-Felix test?
|
Coxiella Burnetii
|
|
Discriminate between endemic and epidemic typhus and what are the causative organisms, as well as where does the rash start
|
endemic, fleas, R. typhi
epidemic, louse, R. prowazeckii Rash starts on the trunk in Typhus, but in the rest of rickettsia it starts on soles and palms, except Q fever, which has no rash |
|
Which Rickettsia does not cause rash?
|
Q fever
spores C. burnetii animal placentas, soil, inhaled aerosoles, pulmonary symptoms |
|
Rickettsial test Weil-Felix may cross react with Ag of what bacterium?
|
with Proteus Ag
|
|
Facial flushing, diarrhea, 3cuspid regurgitation. DX?
|
carcinoid syndrome
commonly arises in appendix, but does not metastasize to liver if arises in terminal ileum, then metastasizes to the liver |
|
What primary cancer commonly metastasizes to the left supraclavicular lymph nodes and the ovaries?
|
Stomach cancer
(Virchow lymph nodes) |
|
A boy with a complain of pain in the knee, blood in the urine and palpable lesions/rash like/purplish on his legs and buttocks. DX?
|
Classical Henoch-Schonlein purpura
IgA anti IgA immune complexes deposition in small vessels and in nephrons, joints |
|
Schilling test?
|
Reabsorption of B12 after orally administering intrinsic factor
(speaking of pernicious anemia) |
|
anti=endomysial
anti-reticulin anti-gliadin antibodies dermatitis herpetiformis |
celiac disease
|
|
Hemochromatosis test and presentation?
|
DMI, bronzed skin, liver cirrhosis, history of diarrhea
do a ferritin test, should be increased it's autosomal recessive |
|
Oligoclonal bands?
|
MS
gamma globulin bands indicative of demyelination lesions in th white matter |
|
generalized pruritus, increased ggt and alkaline phosphatase,
non-tender hepatomegaly |
autoimmune billiary cirrhosis
look for antimitochondrial antibodies COOL: pruritus is due to the deposition of bile salts under the skin |
|
If you give an elderly with type A a type AB transfusion by mistake and he does not hemagglutinate, nor does his blood do so in vitro, what's going on?
|
Elderly often lose the isohemagglutinins such as IgM anti B in this case
normal aging |
|
Name two enzyme deficiencies responsible for hemolytic anemia, in other words, directly affecting health and life of RBCs
|
Glucose 6 phosphate dehydrogenase (for the shunt)
and deficiency in pyruvate kinase, so glycolysis is not possible in the RBC, which does not have mitochondria and does not do TCA |
|
Pyruvate kinase deficiency
|
restricted to RBC
mild to severe chronic hemolytic anemia, which req. blood transfusions |
|
Pyruvate to lactate is the final pathway in which organs/ tissues
|
RBCs, lens of the eye, medulla of the kidney, testes, leukocytes, cornea
|
|
Fate of lactate in myocardium
|
myocardium exclusively oxidizes lactate to CO2 an H2O via the citric acid cycle.
|
|
B1 thiamine f
|
Component of thiamine pyrophosphate, cofactor in:
Pyruvate dehydrogenase (glycolysis) α-ketoglutarate dehydrogenase (TCA cycle) Transketolase (HMP shunt) Branched chain amino acid dehydrogenase |
|
List 2 treatments for hyperammonemia
|
benzoate
phenylbutyrate |
|
A 6 mo old child that presents with mental retardation/deterioration and cherry red spot on the macular, but no hepatospenomegaly
vs a child that presents with the above but with the hepatosplenogmegaly |
cherry red spot in the macula can be seen in Tay-Sachs (Hexoaminidase A def) and Nieman Pick's (sphyngomyelinase def.) but the latter one Neimann Pick's also presents with hepatosplenomegaly
|
|
Differentiate between Hurler's and Hunter's disease
|
Hunter's has no corneal opacities
but it is also x-linked recessive a mucopolysaccharidosis iduronate sulfatase deficiency hepatosplenomegaly, kyphosis,short stature, valvular and ischemic heart disease, CHF, flexion contractures |
|
How do you differentiate hemolytic anemia due to pyruvate kinase deficiency versus G6P dehydrogenase deficiency, which is more common
|
Pyruvate kinase def. caused anemia will not have Heinz bodies
it is also autosomal recessive |
|
HOwell Jollie bodies
|
sickle cell autosplenectomy
in rbc dots |
|
Pale infarcts in which organs?
|
In the ones with single supply
heart kidney spleen |
|
Differentiate between gangrenous necrosis: wet and dry
|
wet (with bacteria)
dry (coagulative ischemic) |
|
Desmoplasia
|
fibrous tissue formation in response to neoplasia
|
|
Plummer-Vinson Syndrome
|
atrophic glossitis
dysphagia iron def. anemia all due to iron deficiency premalignant syndrome high risk for esophageal squamous carcinoma |
|
Tumors associated with tuberous sclerosis
|
astrocytoma
angiomyolipoma cardiac rhabdomyosarcoma |
|
BCL-2
|
follicular and undiff. lymphomas
|
|
c-myc
|
Burkitt's
|
|
ABL
|
CML
|
|
L-myc
|
lung cancer
|
|
n-myc
|
neuroblastoma
|
|
BCL-2
|
follicular and undiff. lymphomas
|
|
erb-B2
|
breast
ovary gastic carcinomas |
|
ras
|
colon carcinoma
|
|
CEA
|
Carcioembryonic antigen
produced by 70 percent of pancreatic and colon cancer also by gastric and breast carcinomas |
|
Lambert=Eaton Syndrome
|
neuromuscular weakness due to the antibodies against pre-synaptic Ca channels
these antibodies are produced by thymomas and small cell lung cancers |
|
ventricular preexcitation syndrome is also known as what?
|
Wolfe-Parkinson-white syndrome
look for delta wave at the onset of qrs Bundle of Kent=accessory pathway between atria and ventricles bypassing AV node can lead to SV tach |
|
Congenital syndrome of long QT with sensorineural deafness is knows as what?
|
Jervell
Lange-Nielsen |
|
Cushing's triad
|
hypertension, bradycardia, respiratory depression
|
|
Turner's syndrome is associated with what congenital cardiac abnormality?
|
coarctation of aorta
|
|
Infant of a diabetic mother has a high risk of what heart abnormality?
|
transposition of great vessels
RtoL cyanotic shunt |
|
Friction rub post MI after 3-5 days?
|
postinfarction fibrinous pericarditis
|
|
Dressler's syndrome
|
autoimmune phenomenon resulting in fibirinous pericarditis several WEEKS after MI,
NOT DAYS |
|
Several weeks after an MI, autoimmune fibrinous pericarditis is called what?
|
Dressler syndrome
|
|
Roth Spots
|
diagnostic of bacterial endocarditis
are white spots on the retina surrounded by hemorrhage |
|
Janeway Lesions
|
can be seen in bac. endocarditis
small erythematous lesions on palm or sole |
|
Osler's nodes
|
can be seen in bact. endocarditis
tender raised lesions on finger or toe pads |
|
what is marantic thrombotic endocarditis?
|
secondary to hypercoagulable state
|
|
Loffler syndrome
|
endomyocardial fibrosis with a prominent eosinnophilic infiltrate
|
|
Libman-Sacks endocarditis
|
the most common manifestation of cardiac SLE
verrucous sterile vegetations on mitral valve, may cause regurg, or stenosis uncomonly SLE causes LSE |
|
Hashimoto's
|
autoimmune
type 4 hypersensitivity antimicrosomal, antithyroglobulin antibodies HLA DR5 Hurthle cells |
|
In Hyperparathyroidism (primary), hypercalcemia predisposes to?
|
peptic ulcer!
|
|
Albright's Hereditary Osteodystrophy
|
autosomal dominant kidney unresponsiveness to PTH
Hypocalcemia, shortened 4th/5th digits, short stature |
|
Kimmelstiel-Wilson nodules
|
This is nodular glomerulosclerosis (the Kimmelstiel-Wilson lesion) of diabetes mellitus. Nodules of pink hyaline material form in regions of glomerular capillary loops in the glomerulus. This is due to a marked increase in mesangial matrix from damage as a result of non-enzymatic glycosylation of proteins
|
|
alfa 2 agonist such as clonidine would have what effect on insulin release?
|
inhibition of insulin release
b2 agonism stimulates the release |
|
IN DKA, hydroxybutyrate: acetoacetate ratio is
|
usually hydroxybutyrate and acetoacetate are produced 1:1
but in pathologic cases such as alcoholism or DM you get more b hydroxybutyrate than acetoacetate |
|
in good pastures, describe renal findings
|
linear immune complex deposits
plus NEPHRITIC syndrome (minor amounts of protein) |
|
Discuss Ghrelin
|
D1/P cells in stomach
lost with gastric bypass surgery regulates appetite increases growth hormone, prolactin, ACTH, cortisol Ghrelin is increased when fasting Ghrelin is decreased after a meal Loss of Ghrelin is associated with hyperphagia in Prader-Willi syndrome |
|
What hormone is responsible for churning and turning sounds in the intestines when one is hungry?
|
motilin, secreted by small intestine
produces migrating motor complexes |
|
What hormone's loss is associated with achalasia?
|
NO
|
|
Copious diarrhea would be seen with what tumor?
|
VIPoma
increases intestinal water and electrolyte secretion relaxation of intestinal smooth muscle and sphincters |
|
Somatostatin is used to treat what tumors?
|
VIPoma and carcinoid tumors
|
|
In cholelithiasis, pain worsens after fatty meals. why?
|
secretion of CCK which increases contractions of the gall bladder
(but decreases gastric emptying) |
|
Warthin's tumor
|
benign salivary tissue trapped in the lymph node , heterotropic
|
|
Peutz-Jeghers
|
autosomal-dominant
multiple nonmalignant hamartomas throughut the GI, along with hyperpigmented mouth, lips, genitalisa, hands. Associated with increasedd risk of CRC and other visceral malignancies |
|
Differentiate Boerhaave's syndrome versus Mallory Weiss
|
In Boerhaave's: rupture of distal esophagus (mostly 75 percent due to endoscopy, complication is pneumomediastinum and Hamman's crunch on PE)
Mallory-Weiss syndrome: mucosal tear of distal esophagus |
|
VATER syndrome
|
vertebral abnormalities
Anal atresia TE tracheoesophageal fistula Renal disorder plus absent radius |
|
Riley-Day Syndrome
|
Familial dysautonomia
autosomal recessive mostly in Jewish children unstable blood pressure, difficulty feeding, abnormal sweating, orthostatic hypotension, progressive sensory loss results from loss of neurons in the autonomic and sensory ganglia |
|
Shy-Drager syndrome
|
preganglionic sympathetic neurons form the intermediolateral cell column
it is characterized by orthostatic hypotension, anhidrosis, impostence, and bladder atonicity |
|
Migratin thrombophebitis
|
carcinoma
pancreatic or lung |
|
Heyde's Syndrome
|
syndrome of aortic valve stenosis associated with gastrointestinal bleeding from colonic angiodysplasia. It is named after Dr. Edward C. Heyde, who first described the association in 1958.[1] It is due to the induction of von Willebrand disease type IIA by the valvular stenosis.[2]
|
|
When aortic stenosis is associated with lower GI bleeding (colonic angiodysplasia) what is the syndrome's name?
|
Heyde's syndrome
|
|
Megadoses of what vitamin are associated with reduced synthesis of K-dependent clotting factors and thus are synergistic with warfarin?
|
vitamin E
|
|
Excess of what vitamin in the mother can cause hemolytic anemia and jaundice in a newborn?
|
vitamin K
|
|
Effects of vitamin E deficiency
|
hemolytic anemia
spinocerebellar tract/ dorsal column degeneration and peripheral neuropathy plus ataxia |
|
Vitamin B2 deficiency symptoms
|
glossitis
angular stomatitis cheilosis corneal neovascularization |
|
vitamin deficiency and vision
|
corneal neovascularization in vitamin b2 riboflavin deficiency
corneal squamous metaplasia in vtimain A deficiency plus since it's a componenet of rhodopsin you get night blindness |
|
Biotin deficiency symptoms
|
dermatitis alopecia
lactic acidosis |
|
SE of niacin supplementation in hypercholesterolemia?
|
flushing
intrahepatic cholestasis |
|
Hand-Schuller-Christian
(histiocytosis) |
exophthalmos
diabetes insipidus bone lytic lesions |
|
dermatomyositis in a middle aged man is associated with what?
|
epithelial cancer
like lung carcinoma inclusion myositis or polymyositis are not associated with malignancy |
|
inclusion body myositis is resistant to what tx?
|
corticosteroids, but really to none
|
|
eaton lambert syndrome assn
|
ab to ca channel releasing ach
muscle weakness does not improve with ache inhibitor unlike with myasthenia gravis (which often has a thymoma, which resection is curative) eaton lambert is associated with small cell lung carcinoma |
|
Neimann Pick's
|
progressive neurodegenerative
cherry red spot on macular hepatosplenomegaly FOAM CELLS Autosomal Recessive Sphingomyelinase deficiency |
|
Fabry's disease
|
painful neuropathies
corneal opacities renal/cardiac problems angiokeratomas/ diffuse violaceous skin rash alfa galactosidase A (ceramide trihexoside accumulates) X linked recessive the only one |
|
Metachromatic leukodystrophy
|
arylsulfatase A
|
|
Krabbe's disease
|
globoi cells in degenerating white matter
galactocerebrosidase AR peripheral neuropathy developmental dealy |
|
what enzymes are defficient in Neiman Pick's vs Krabbe's
|
Neimann Picks sphyngomyelinase
Krabbe's galactocerebrosidase Mr. Neimann |
|
DX: pot-bellied, pale, puffy faced child with protruding umbilicus and protuberant tongue
|
cretinism due to hypothyroidism (endemic goiter/ no iodine in the diet)
|
|
Jod-Basedow phenomenon
|
thyrotoxicosis if a patient with iodine deficiency goiter is made iodine replete
|
|
Hypercalcemia is co-present in these 2 disorders
|
zollinger-ellison (co present hyperparathyroidism)
addison's (evidently normal physiological levels of cortisol are necessary to decrease bone resorption and activate vitamin D) |
|
Hypercalcemia can be a result of excess of these 2 vitamins
|
Vit D of course
VITAMIN A |
|
Albright's hereditary osteodystrophy
|
pseudohypoparathyroidism
autosomal dominant unresponsiveness to PTH short stature, shortened 4,5 metatarsals/ digits, hypocalcemia (and I think mental retardation mild often) |