Classic Presentations (First Aid Rapid Review) Flashcards
Abdominal pain
Ascites
Hepatomegaly
Budd-Chiary syndrome
post-hepatic venous thrombosis
Achilles tendon xanthoma
Familial hypercholesterolemia
decreased LDL receptor signaling
Adrenal hemorrhage
Hypotension
DIC
Waterhouse-Friderichsen syndrome
Meningococcemia
Arachnodactylyl
Lens dislocation
Aortic dissection
Hyperflexible joints
Marfan’s syndrome
Fibrillin defect
Athelete w/ polycythemia
Secondary to erythropoietin injection
Back pain
Fever, Night Sweats, Weight Loss
Pott disease
Vertebral TB
Bilateral hilar adenopathy
Uveitis
Sarcoidosis
Noncaseating granuloma
Blue sclera
Osteogenesis imperfecta (type I collagen defect)
Bluish line on gingiva
Burton line
Lead poisoning
Bone pain
Bone enlargement
Arthritis
Paget disease of bone
Increased osteoblastic and osteoclastic activity
Bounding pulses
Diastolic heart murmur
Head bobbing
Aortic regurgitation
“Butterfly” facial rash
Raynaud phenomenon
Young female
Systemic lupus erythematosus
Cafe-au-lait spots Lisch nodules (iris hamartoma)
Neurofibromatosis type I
+ pheochromcytoma, optic gliomas
Cafe-au-lait spots
Polyostotic fibrous dysplasia
Precocious puberty
Multiple endocrine abnormalities
MuCune-Albright syndrome
mosaic G-protein signaling mutation
Calf pseudohypertrophy
Muscular dystrophy (m/c Duchenne) (X-linked recessive deletion of dystrophin gene)
“Cherry-red spots” on macula
Tay-Sachs (ganglioside accumulation)
or
Niemann-Pick (sphingomyelin accumulation)
Central retinal artery occlusion
Chest pain on exertion
Angina
stable: with moderate exertion
(unstable: with minimal exertion)
Chest pain
Pericardial effusion/friction rub
Persistent fever following MI
Dressler syndrome
(AI-mediated post-MI fibrinous pericarditis)
(1-12wks after acute episode)
Child uses arms to stand up from squat
Gowers sign
Duchenne muscular dystrophy
Child w/ fever later develops red rash on face that spreads to body
“Slapped cheeks”
Erythema infectiosum/fifth disease: parvovirus B19
Chorea
Dementia
Caudate degeneration
Hungtinton disease (Autosomal dominant CAG repeat expansion)
Chronic exercise intolerance w/: Myalgia Fatique Painful cramps Myoglobinuria
McArdle disease (Muscle glycogen phosphorylase deficiency)
Cold intolerance
Hypothyroidism
Conjugate lateral gaze palsy
Horizontal diplopia
Internuclear opthalmoplegia
Damage to MLF; bilateral [Multiple sclerosis], unilateral [stroke]