A. membranoprołiferative glomerulonephritis d> IgA nephropathy
C. Membranous glomerulonephritis
D. Minimal change disease
E. Post-infectious glomerulonephritis
A. liver and spleen ĘL heart with valves (2P skin and joints D. distal parts of fmgers
A. There are three types of MPGN: type I is characterized by mesangial and subendothelial immune deposits, type II by deposits in lamina densa of the basement membranę, whereas type III is very uncommon and characterized by features of both previous types.
B. For type I of MPGN most common clinical manifestation is nephritic syndrome
C. In type II acute nephritis or hematuria are most common presentations
© Type I is often idiopathic and relatively rare associated with systemie disease, infection and neoplasmas.
A. most common cause of nephritic syndrome in childhood
B. mc ) C. mo: ^ <£> itis
B. in clinical onset it might be associated with upper respiratory infection or prophylactic immunizations most patients respond to steroids
: is highiy associated with the occurance ofrenal failure E. proteinuria is composed mostly of albumins (“selective” proteinuria)
12
h
CAj is most common childhood kidney disease
B. comprises 10% of childhood and up to 20% of cases idiopathic nephritic syndrome
C. mostly appears in subjects in high glomerular filtration ratę
D. commonly recurs after transplantation
' i
A. because high avidity Fc receptors are present on glomerular basement membranę that allows immunophagocytosis d> because blood flow in kidney is extremely slow and in glomeruli there are many sinusoids that allows easier antibody up-taking from the blood
C. because it has a rich blood supply and fenestrated capillary bed
D. because in kidney there is a high concemration of denritic cells that are able to capture antigens and antibodies present in bloodstream
14.
A. p2-microglobulin
HLA-A, HLA-B. and HLA-C
C.
D.
E.
HLA-A and HLA-C HLA-DR, -DP, and -DQ H-2 IA and IE
B.
A. erythrocytes platelets leukocytes endothelial dells
E. dendritic cells