UWorld 2nd time incorrects Flashcards
(533 cards)
cafe-au-lait spots
neurofibromas
Lisch nodules (pigmented, asymptomatic hamartomas of the iris)
congenital pseudoarthritis
other associated tumors: meningiomas, astrocytomas, glioma, pheochromocytomas
NF-1 (single gene autosomal dominant on chromosome 17)
what is the mechanism of insulin resistance
phosphorylation of serine and threonine residues of insulin receptor substrate by serine kinase
the serine and threonine on the beta subunit of the insulin receptor is phosphorylated in order to decrease the cellular cascade that allows the GLUT4 receptor to come to the cell surface
-this type of phosphorylation is induced by TNF-alpha , catecholamines, glucocorticoids, and glucagon
describe the structure of the insulin receptor
2alpha nd 2beta subunits
the 2 alpha are extracellular and act as binding sites for the insulin
the 2beta subunits act as intracellular and have tyrosine binding domains that are activated when insulin binds to the alpha subunits
-the insulin receptor is the autophosphorylated and GLUT4 is transported to the membrane to allow glucose into the cell
compare and contrast polymyalgia rheumatica vs fibromyalgia
PR–> pain and stiffness in proximal muscles with fever, malaise, and weight loss. no muscle weakness. women >50. associated with giant cell temporal arteritis. symptoms get better with steroids
FM–> women 20-50. chronic widespread musculoskeletal pain associated with tender points, stiffness, paresthesias, poor sleep, fatigue, cognitive disturbance (fibro fog). treat with regular exercise, antidepressants (TCAs and SNRIs), neuropathic pain agents (gabapentin)
list the retroperitoneal organs
SAD PUCKER
Suprarenal (adrenal) glands
Aorta & inferior vena cava
Duodenum (except first part)
Pancreas (head and body) Ureters & bladder Colon (ascending and descending) Kidneys Esophagus Rectum (mid and distal)
what are the symptoms and whats the pathogenesis of multiple myeloma
SYMPTOMS: renal insufficiency, back/bone pain, normocytic anemia, hypercalcemia
PATHOGENESIS: excessive production of monoclonal immunoglobulin (paraprotein), myeloma cells replicate in the bone marrow and release cytokines to activate osteoclasts and inhibit osteoblasts (via IL3, IL7, and Wnt pathway inhibition) leading to osteolytic (radiolucent) bone lesions
myeloma cells stimulate osteoclast maturation by producing RANKL and destroying OPG
this destruction of bone leads to the hypercalcemia seen
inheritance pattern of hemophilia a, b, and c
a (8) and b (9) –> x-linked recessive
c (11) –> autosomal recessive
pt with central venous catheter and parenteral nutrition (lots of pokes into their skin) are more likely to have what fungal infection and how does it look
candida –> pseudohyphae with blastoconidia
bacterial endotoxin
lipopolysaccharide found in gram negative bacteria that is released upon cell lysis
-in blood stream it causes severe inflammatory response mediated by TNF-alpha and IL-1 secreted by macrophages
stacked brick intestinal adhesion
enteroaggregative E.coli (adhere but dont invade intesintal mucosa)
-persistant diarrhea in infants in developing countries and in those with advanced AIDS
what to look out for in patients taking second generation atypical antipsychotics
-apines –> metabolic syndrome (weight gain, diabetes, hyperlipidemia)
clozapine –> agranulocytosis
risperidone –> hyperprolactinemia (amenorrhea, galactorrhea, gynecomastia)
what should you think of if you see ANA and anti-histone antibodies and whats implicated in this
drug induced lupus erythematous
- procainamide and hydralazine are the two most common
- isoniazid, minocycline, and quinidine are also implicated
circumferential laxity of phrenoesophageal membrane
sliding hiatal hernia
phrenoesophageal membrane defect can lead to what
paraesophageal hiatal hernia (herniated gastric fundus)
bochdalek hernia
failure of posterolateral diaphragmatic foramina to fuse
- congenital hernia diagnosed pre or perinatally
- pulmonary hypoplasia with neonatal respiratory distress is common
lesser sac hernia
herniation of viscera through omental foramen (foramen of winslow) causes intraabdominal hernia
-rare and usually involve small bowel and are very painful due to bowel strangulation
most common benign liver mass
cavernous hemangioma (venous malformation)
- usually occurs b/w ages 30-50
- usually filled with thrombus and incidentally found
- biopsy contraindicated due to risk of hemorrhage
female with pulse discrepancies in upper extremities, fever, night sweats, arthritis, myalgias, skin nodules, ocular disturbances
takayasu arteritis
- granulomatous thickening and narrowing of aortic arch and proximal great vessels
- increase in ESR
- treat with corticosteroids
pseudomembranous colitis (white yellow plaques with fibrin and inflammatory cells)
clostridium difficile
what two enzymes can act on homocysteine
- methionine synthase (requires B12)
- cystathionine synthase (requires B6) –> this defect is the most common cause of homocysteinuria (causing an increase in methionine)
-note: homocysteine is prothrombotic resulting in premature thromboembolic events (atherosclerosis and acute coronary syndrome)
young pt with heart attack, what do you think?
homocystinuria or kawasakis
how is scar tissue formed
macrophages secrete TGF-beta to stimulate fibroblasts to secrete collagen and form scar tissue
major component of eosinophilic granules
major basic protein that works against helminths
what class of medication should you not prescribe to a pt who has a history of gall stones
fibrates (reduce cholesterol solubility and promote gallstone formation by reducing bile acid synthesis)