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]
Continuous “machine-like” heart murmur
PDA
(Close w/ indomethacin)
(Open or maintain w/ misoprostol)
Cutaneous/dermal edema due to CT deposition
Myxedema
Caused by hypothyroidism, Graves disease [pretibial]
Dark purple skin/mouth nodules
AIDS patient
Kaposi sarcoma
associated w/ HHV-8
Deep, labored breathing/hyperventilation
Kussmaul respiration (diabetic ketoacidosis)
Dermatitis
Dementia
Diarrhea
Pellagra
niacin [vitamin B3] deficiency
Dilated cardiomyopathy
Edema
Alcholism or malnutrition
Web berberi (thiamine [vitamin B1] deficiency)
Dog or cat bite resulting in infection
Pasteurella multocida
cellulitis at inoculation site
Dry eyes
Dry mouth
Arthritis
Sjogren syndrome (AI destruction of exocrine glands)
Dysphagia (esophageal webs)
Glossitis
Iron deficiency anemia
Plummer-Vinson syndrome
may progress to esophageal squamous cell carcinoma
Elastic skin
Hypermobility of joints
Ehlers-Danlos syndrome
Type III collagen defect
Enlarged, hard left supraclavicular node
Virchow node (Abdominal metastasis)
Erythroderma
Lymphadenopathy
Hepatosplenomegaly
Atypical T cells
Mycosis fungoides (cutaneous T-cell lymphoma) or Sezary syndrome (mycosis fungoides + malignant T cells in blood)
Facial muscle spasm upon tapping
Chvostek sign
Hypocalcemia
Fat
Female
Forty
Fertile
Cholelithiasis
gallstones
Fever, Chills
Headache
Myalgia following antibiotic tx for syphilis
Jarisch-Herxheimer reaction
rapid lysis of spirochetes results in toxin release
Fever Cough Conjunctivitis Coryza Diffuse rash
Measles
Fever
Night sweats
Weight loss
B symptoms (staging) of lymphoma
Fibrous plaques in soft tissue of penis
Peyronie disease
CT disorder
Gout
Intellectual disability
Self-mutilating behavior in a boy
Lesch-Nyhan syndrome
(HGPRT deficiency)
(X-linked recessive)
Green-yellow rings around peripheral cornea
Kayser-Fleischer rings
Copper accumulation from Wilson disease
Hamartomatous GI polyps
Hyperpigmentaiton of mouth/feet/hands
Peutz-Jeghers syndrome
(Inherited, benign polyposis can cause bowel obstruction)
(Increased cancer risk, mainly GI)
Hepatosplenomegaly
Osteoporosis
Neurologic symptoms
Gaucher disease (Glucocerebrosidase deficiency)