rapid review COPY Flashcards
abdominal pain
ascities
hepatomegaly
budd chiari syndrome
post hepatic venous thrombosis
abdominal pain
diarrhea
leukocytosis (WBCs up)
recent abx
c diff infection
achilles tendon xanthoma
familial hypercholesterolemia
decrease LDL receptor signalling
adrenal hemorrhage
hypotension
DIC
waterhouse friderichsen syndrome
meningococcemia
anaphylaxis following blood transfusion
IgA def
anterior “drawer sign” positive
ACL injury
arachnodactyly
lens dislocation upward
aortic dissection
hyperflexible joints
marfans syndrome
fibrillin defect
athlete with polycythemia
secondary to erythropoietin injection
back pain
fever
night sweats
potts disease
vertebral TB
bilateral acoustic scwannomas
neurofibromatosis type 2
bilateral hilar adenopathy
uveitis
sarcoidosis
noncaseating granulomas
black eschar on face of patient with DKA
mucor or rhizopus fungal infection
blue sclera
osteogenesis imperfecta
type 1 collagen defect
bluish line on gingiva
burton line
lead poisoning
bone pain
bone enlargement
arthritis
paget disease of bone
increased OB and OC activity
bounding pulses
wide pulse pressure
diastolic heart murmur
head bobbing
aortic regurg
“butterfly” facial rash
raynaud phenomenon
young female
SLE
cafe au lait spots lisch nodules (iris hamartoma) cutaneous neurofibromas pheochromocytoma optic gliomas
neurofibromatosis type 1
cafe au lait spots (unilateral)
polyostotic fibrous dysplasia
precocious puberty
multiple endocrine abnormalities
McCune Albright syndrome
mosaic G protein signaling mutation
calf pseudohypertrophy
muscular dystrophy
most commonly duchenne
due to x linked recessive frameshift mutation of dystrophin gene
cervical LAD desquamating rash coronary aneurysms red conjunctiva and tongue hand foot changes
kawasaki disease
treat with IVIG and aspirin
“cherry red spots” on macula
Tay sachs (ganglioside accumulation)
or
niemann pick (sphingomyelin accumulation)
due to central retinal artery occlusion
chest pain on exertion
angina
stable= with moderate exertion
unstable= with minimal exertion or at rest
chest pain
pericardial effusion/friction rub
persistent fever following MI
dressler syndrome
autoimmune mediated post MI fibrinous pericarditis
2 weeks to several months after an acute episode