UWorld Flashcards
IFN-gamma
released by T cells
use it to test for latent TB (how much IFN-gamma is released by T cells when exposed to TB antigens?)
Enteric bacteremia = most likely to be caused by
E coli, Salmonella typhi, Klebsiella, proteus (shigella is rarely phagocytosed and destroyed when it enters bloodstream, so no bacteremia)
DSM5 personality disorders
Paranoid = suspicious, distrustful, hypervigilant
Schizoid = loner, detached, unemotional
Schizotypal = eccentric; odd thoughts, perceptions and behavior
Antisocial = disregard and violation of rights of others
Borderline = chaotic relationships, labile mood, inner emptiness, self harm etc
Histrionic = dramatic, superficial, attention seeking
Narcissistic = grandiose, lack empathy
avoidant = avoid b/c of fears of criticism and rejection
Dependent = submissive, clingy
Obsessive-compulsive = rigid, controlling, perfectionistic
To locate appendix intra-op?
follow tenia coli band of muscle to where it attaches to cecum
Stimulation of pancreatic bicarb release?
Enzyme release?
Bicarb = from secretin (secreted by S-cels in response to increasing H+ conc)
Enzymes = from CCK and cholinergic stim
Wiskoff-Aldrich
eczema, recurrent infxns, thrombocytopenia
mut on X chrom (males) - combo B and T lymphocyte disorder
tx = hla-matched bone marrow transplant
HUS
microangiopathic hemolytic anemia, thrombocytopenia, acute renal failure
usually caused by enteroinvasive infxn –> toxin binds renal endothelium –> damage –> thrombosis and inactivation of ADAMTS13 (as in TTP) –> growing thrombi –> RBC lysis (schistocytes) and AKI (uremia)
causes of aplastic anemia
chloramphenicol use
infection of SCD pts with parvo
Chediak-Higashi syndrome
albinism, peripheral neuropathy, immunodeficiency
phagocyte dysfxn
ataxia-telangectasia syndrome
B/T cell defect –> ataxia and telangectasia
3’–> 5’ exonuclease vs 5’ –> 3’ exonuclease
Prokaryotes have 3 DNA polymerases and all have 5’-to-3’ polymerase and 3’ to 5’ proofreading exonuclease activity, but DNA pol 1 also has 5’ to 3’ exonuclease activity
5’–>3’ allows DNA pol1 to do nick translation (DNA repair and removal of RNA primers)
3’–>5’ is the usual virus-encoded proofreader; absent in HCV so it makes lots of replication errors –> lots of subspecies of HCV
Lithium effects on kidney
induces DI by antagonizing vasopressin/ADH (–> polydipsia, polyuria, inappropriately dilute urine after water restriction)
in addition to kidney damage, can cause hypothyroidism (monitor BUN, Cr, and thyroid fxn)
*lithium toxicity enhanced by anything that decreases GFR –> increased PT lithium reabs (lithium follows Na) –> increased lithium floating around in the body, and it has a really narrow therapeutic window
**ACEi, NSAIDs and nondihydropyridine CCBs can also increase lithium conc and toxicity
Abciximab is used for…
GPIIb/IIIa antag, used for unstable angina and ACS
Direct thrombin inhibitors are used in
argatroban (HIT), dabigatran (afib, venous thromboembolism)
so anticoag
clopidogrel vs abciximab
clopidogrel blocks ADP receptors on plts
abciximab blocks GPIIb/IIIa
Symptoms of Patau syndrome
holoprosencephaly (ranging from cleft lip to cyclops), microceph, microphthalmia, ID
Markedly elevated AFP levels associated with ___
open neural tube and ventral wall defects (eg opmhalocele, gastroschisis)
vs low AFP associated with Down syndrome
Parinaud syndrome
dorsal midbrain problem (paralysis of upward gasze, kptosis and pupillary abnormalities) due to compression of pretectal region of midbrain, eg from pineal gland mass
most common pineal gland mass?
germinoma (from embryonic germ cells); most common in young boys
also seen in suprasellar region (less common) –> endocrine problems
Ventral vs dorsal pancreatic buds
dorsal forms majority of pancreatic tissue, + accessory duct (which usually fuses with ventral duct and rest of it usually degenerates, except in pancreas divisum, when the buds fail to fuse, so there are two ducts into duod; usu asymptomatic but can –> recurrent pancreatitis)
ventral = major duct + inferior/posterior portion of head and uncinate process
Myotonia
abnormally slow relaxation of muscles
Sx: difficulty loosening one’s grip, cataracts, frontal balding, gonadal atrophy
myotonic muscular dystrophy (second most common inherited muscle disorder, aut dom trinucleotide repeat expansion of gene for myotonia protein kinase)
type 1 fibers = esp atrophied
Inflammatory myopathies
Dermatomyositis, polymyositis
Ion channel myopathies
sx: myotonia (abnormally slow relaxation of mm) + episodes of hypotonoic paralysis, esp with exercise; no muscle atrophy