A Case Report of Crescentic Glomerulonephritis With Positive Serum Anti-glomerular Basement Membrane Without Linear Glomerular Basement Membrane Immunofluorescent Staining.

acute glomerulonephritis acute renal injury anti-gbm glomerular disorders necrotizing and crescentic glomerulonephritis

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
May 2022
Historique:
accepted: 10 05 2022
entrez: 15 6 2022
pubmed: 16 6 2022
medline: 16 6 2022
Statut: epublish

Résumé

Anti-glomerular basement membrane (anti-GBM) disease is an autoimmune disorder characterized by the production of circulating immunoglobulin G (IgG) antibodies that affect the kidneys and lungs, mainly in the form of rapidly progressive crescentic glomerulonephritis and pulmonary hemorrhage. Typically diagnosed on tissue biopsy, findings mainly include glomerular crescent formation, bright linear staining of GBM for IgG on direct immunofluorescence (IF), and the serologic presence of circulating anti-GBM antibodies. Variation in the laboratory results, where histological findings of linear IgG IF staining were present in the absence of circulating anti-GBM antibodies, have recently led to the use of the term "atypical anti-GBM disease," which usually has a distinct benign clinical outcome as compared to typical anti-GBM disease. We report a case of a middle-aged woman who presented with renal failure without lung involvement. Upon further investigation, the patient was found to have strongly positive serum anti-GBM antibodies, but the tissue biopsy did not show typical findings of the anti-GBM disease. The patient showed modest improvement after multiple sessions of plasmapheresis and steroids, with stabilization of her renal parameters after the initial response. In our case, we will address the possibilities of the discrepancies between the serological and histopathological findings.

Identifiants

pubmed: 35702466
doi: 10.7759/cureus.24879
pmc: PMC9179943
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e24879

Informations de copyright

Copyright © 2022, Faisal et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Kidney Int. 2016 Apr;89(4):897-908
pubmed: 26994577
J Autoimmun. 2014 Feb-Mar;48-49:108-12
pubmed: 24456936
Kidney Int. 2004 Oct;66(4):1535-40
pubmed: 15458448
J Am Soc Nephrol. 1999 Nov;10(11):2446-53
pubmed: 10541306
BMC Nephrol. 2018 Sep 12;19(1):228
pubmed: 30208856
BMC Nephrol. 2018 Oct 22;19(1):286
pubmed: 30348108
Nephrol Dial Transplant. 2000 Aug;15(8):1238-41
pubmed: 10910453
Am J Kidney Dis. 2005 Feb;45(2):397-406
pubmed: 15685519
Nephron Clin Pract. 2003;94(3):c59-68
pubmed: 12902632
Kidney Int. 2006 Dec;70(12):2148-51
pubmed: 17063172
Kidney Int. 1994 Mar;45(3):721-6
pubmed: 8196274
Springer Semin Immunopathol. 2003 May;24(4):345-61
pubmed: 12778332

Auteurs

Mohannad Faisal (M)

Internal Medicine, Hamad Medical Corporation, Doha, QAT.

Abdullah Shams (A)

Internal Medicine, Hamad Medical Corporation, Doha, QAT.

Suresh Archichige (S)

internal Medicine, Hamad Medical Corporation, Doha, QAT.

Ahmed Hamdi (A)

Nephrology, Hamad Medical Corporation, Doha, QAT.

Mohammed Akhtar (M)

Laboratory Medicine and Pathology, Hamad Medical Corporation, Hamad General Hospital, Doha, QAT.

Classifications MeSH