Glomerular Disease

Question 1

too many mesnagial and endothelial cells, immune complex deposition

Answer 1

intrinsic hypercellularity

Question 2

crescents, rupture of GBM

Answer 2

extrinsic hypercellularity

Question 3

result of endothelial injury, immune complexes, new BM

Answer 3

double contours

Question 4

DM and HTN, anitbody or immune complexes

Answer 4

mesangial matrix accumulation

Question 5

capillary, mesnagial, or linear pattern

Answer 5

immune complex deposition

Question 6

caused by lupus, HTN, DIC

Answer 6

thrombosis

Question 7

hematuria, HTN, increased serum creatinine

Answer 7

nephritic syndrome

Question 8

proteinuria, edema, hyperlipidemia, hypoalbuminemia

Answer 8

nephrotic syndrome

Question 9

diffuse crescents, common immune injury, nephritic syndrome usually

Answer 9

RPGN

Question 10

BM thickening, Kimmelsteil-Wilson nodules (hyaline, acellular), commonly with HTN

Answer 10

diabetic nephropathy

Question 11

thickening of vessel intima

Answer 11

chronic hypertensive glomerulopathy

Question 12

nephrotic syndrome, global thickening of capillary loops, in situ immune complexes, IgG in capillary pattern, secondary to drugs, infections, neoplasms

Answer 12

membranous glomerulopathy

Question 13

nephritic/nephrotic syndrome, renal failure, full house inclusion bodies, DNA/RNA antigens

Answer 13

Lupus

Question 14

recurrent hematuria with upper respiratory infection, mesangial expansion

Answer 14

IgA nephropathy

Question 15

diffuse lobar hypercellularity, abnormal complement, double contours, hep-C

Answer 15

membranoproliferative glomerulonephritis

Question 16

after strep, nephritis and resp symtoms, hematuria, decreased complement, proteinuria

Answer 16

post infectious glomerulonephritis