Pan-nephritis (glomerulonephritis, arteriolitis, and tubulointerstitial nephritis) associated with predominant mesangial C1q deposition and hypocomplementemia: a variant type of C1q nephropathy?

doi:10.1016/s0272-6386(96)90171-7

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Article

Pan-nephritis (glomerulonephritis, arteriolitis, and tubulointerstitial nephritis) associated with predominant mesangial C1q deposition and hypocomplementemia: a variant type of C1q nephropathy?

American journal of kidney diseases : the official journal of the National Kidney Foundation - 1 Apr 1996

Imai H, Yasuda T, Satoh K, Miura A B, Sugawara T, Nakamoto Y

Abstract excerpt

A 35-year-old man showed acute nephritic syndrome manifested as proteinuria, hematuria, and hypocomplementemia after upper respiratory infection. A renal biopsy showed mild to moderate mesangial proliferative glomerulonephritis with an accumulation of mononuclear cells in the capillary loop and w...

Topics

Adult
Arterioles
Arteritis
Biopsy
Complement C1q
Complement C3
Diagnosis, Differential
Fibrinogen
Glomerular Mesangium
Glomerulonephritis, Membranoproliferative
Humans
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M

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Kidney

Male

Nephritis, Interstitial

Phenotype

Source

Open in PubMed

Identifiers

PMID: 8678071
DOI: 10.1016/s0272-6386(96)90171-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8678071-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.