TY - JOUR
T1 - Mixed-Pattern Immune Deposit Glomerulonephritis in a Child With Inherited Deficiency of the Third Component of Complement
AU - Borzy, Michael S.
AU - Houghton, Donald
N1 - Funding Information:
From the Departmellt of Pediatrics. Doernbecher Memorial Hospitalfor Children. Oregon Health Sciences University, and the Department of Pathology; Oregon Health Sciences University. Supported in part by grants from the Oregon Chapter of the American Cancer Society and the Medical Research Foundation of Oregon. Address reprint requests to Michael S. Borzy. MD. Division of Pediatric Immunology/Rheumatology. Departmellf of Pediatrics. Doernbecher Memorial Hospital for Children. Oregon Health Sciences University. 3181 SW Sam Jackson Park Rd, Portland, OR 97201. © 1985 by The National Kidney Foundation. Inc. 0272-6386/85/010054-06$3.00/0
PY - 1985
Y1 - 1985
N2 - The renal histopathology of a 7-year-old Laotian male with inherited deficiency of the third component of complement, recurrent infections, and persistent hematuria and proteinuria is described. The histologic changes are predominantly those of mesangiopathic disease with isolated changes resembling type I membranoproliferative glomerulonephritis and transmembranous glomerulonephritis. IgG, IgA, IgM, C4, and fibrinogen, but not C3, were detected by immunofluorescence in mesangial zones and in segments of capillary walls. A normal distribution of C3b receptors was present along all capillary walls. This report provides additional support for the association of congenital C3 deficiency and immune deposit glomerulonephritis.
AB - The renal histopathology of a 7-year-old Laotian male with inherited deficiency of the third component of complement, recurrent infections, and persistent hematuria and proteinuria is described. The histologic changes are predominantly those of mesangiopathic disease with isolated changes resembling type I membranoproliferative glomerulonephritis and transmembranous glomerulonephritis. IgG, IgA, IgM, C4, and fibrinogen, but not C3, were detected by immunofluorescence in mesangial zones and in segments of capillary walls. A normal distribution of C3b receptors was present along all capillary walls. This report provides additional support for the association of congenital C3 deficiency and immune deposit glomerulonephritis.
KW - C3 deficiency
KW - immune deposits
KW - mesangiopathic glomerulonephritis
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U2 - 10.1016/S0272-6386(85)80137-2
DO - 10.1016/S0272-6386(85)80137-2
M3 - Article
C2 - 3155591
AN - SCOPUS:0021990023
SN - 0272-6386
VL - 5
SP - 54
EP - 59
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 1
ER -