Classic Labs/findings part 1 Flashcards
Colonies of mucoid Pseudomonas in lungs
Cystic fibrosis (autosomal recessive mutation in CFTR gene --> fat-soluble vitamin deficiency and mucous plugs)
Decreased AFP in amniotic fluid/maternal serum
Down syndrome, Edwards syndrome
Increased β-hCG,
Decreased PAPP-A on first trimester screening
Down syndrome
Increased serum homocysteine, increased mehtylmalonic acid, decreased folate
Vitamin B12 deficiency
Anti-histone antibodies
Drug-induced SLE (eg, hydralazine, isoniazid, phenytoin, TNF-α inhibitors)
Low T cells, low PTH, low Ca2+, absent thymic shadow on CXR
Thymic aplasia (DiGeorge syndrome, velocardiofacial syndrome)
Large granules in phagocytes, immunodeficiency
Chédiak-Higashi disease (congenital failure of phagolysosome formation)
Recurrent infections, eczema, thrombocytopenia
Wiskott-Aldrich syndrome
Optochin sensitivity
Sensitive: S pneumoniae;
Resistant: viridans streptococci (S mutans, S sanguis)
Novobiocin response
Sensitive: S epidermidis;
Resistant: S saprophyticus
Bacitracin response
Sensitive: S pyogenes (group A);
Resistant: S agalactiae (group B)
Branching gram ⊕ rods with sulfur granules
Actinomyces israelii
Hilar lymphadenopathy, peripheral granulomatous lesion
in middle or lower lung lobes (can calcify)
Ghon complex (1° TB: Mycobacterium bacilli)
“Thumb sign” on lateral neck x-ray
Epiglottitis (Haemophilus influenzae)
Bacteria-covered vaginal epithelial cells
“Clue cells” (Gardnerella vaginalis)