Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review

Anti-glomerular basement membrane (GBM) disease is a rare autoimmune condition characterized by the presence of positive anti-GBM autoantibodies, linear deposition of immunoglobulin G (IgG) along the GBM and severe kidney injury. In a limited number of cases, the association of anti-GBM disease with...

Full description

Saved in:
Bibliographic Details
Main Authors: Zewei Chen, Dechao Xu, Fangzheng Cui, Huihui Hou, Zhiguo Mao, Xiang Gao
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Renal Failure
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/0886022X.2024.2323160
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832591110070861824
author Zewei Chen
Dechao Xu
Fangzheng Cui
Huihui Hou
Zhiguo Mao
Xiang Gao
author_facet Zewei Chen
Dechao Xu
Fangzheng Cui
Huihui Hou
Zhiguo Mao
Xiang Gao
author_sort Zewei Chen
collection DOAJ
description Anti-glomerular basement membrane (GBM) disease is a rare autoimmune condition characterized by the presence of positive anti-GBM autoantibodies, linear deposition of immunoglobulin G (IgG) along the GBM and severe kidney injury. In a limited number of cases, the association of anti-GBM disease with other glomerulonephritis has been reported. Herein, we present the case of a 66-year-old female patient with progressive worsen kidney function and decreased urine output. A renal biopsy revealed crescent glomerulonephritis with lineal IgG deposition along the GBM and mesangial IgA deposition, which supported the diagnosis of concurrent anti-GBM disease and IgA nephropathy (IgAN). In an extensive literature review, we identified a total of thirty-nine patients were reported anti-GBM disease combined with IgAN. The clinical characteristics of these patients demonstrate that the anti-GBM disease combined with IgAN tends to be milder with a more indolent course and a better prognosis than the classic anti-GBM disease, and its potential pathogenesis deserves to be further explored.
format Article
id doaj-art-868e70932a4d40d8b62959d396b48e76
institution Kabale University
issn 0886-022X
1525-6049
language English
publishDate 2024-12-01
publisher Taylor & Francis Group
record_format Article
series Renal Failure
spelling doaj-art-868e70932a4d40d8b62959d396b48e762025-01-23T04:17:48ZengTaylor & Francis GroupRenal Failure0886-022X1525-60492024-12-0146110.1080/0886022X.2024.2323160Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature reviewZewei Chen0Dechao Xu1Fangzheng Cui2Huihui Hou3Zhiguo Mao4Xiang Gao5Kidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaKidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaKidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaKidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaKidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaKidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, ChinaAnti-glomerular basement membrane (GBM) disease is a rare autoimmune condition characterized by the presence of positive anti-GBM autoantibodies, linear deposition of immunoglobulin G (IgG) along the GBM and severe kidney injury. In a limited number of cases, the association of anti-GBM disease with other glomerulonephritis has been reported. Herein, we present the case of a 66-year-old female patient with progressive worsen kidney function and decreased urine output. A renal biopsy revealed crescent glomerulonephritis with lineal IgG deposition along the GBM and mesangial IgA deposition, which supported the diagnosis of concurrent anti-GBM disease and IgA nephropathy (IgAN). In an extensive literature review, we identified a total of thirty-nine patients were reported anti-GBM disease combined with IgAN. The clinical characteristics of these patients demonstrate that the anti-GBM disease combined with IgAN tends to be milder with a more indolent course and a better prognosis than the classic anti-GBM disease, and its potential pathogenesis deserves to be further explored.https://www.tandfonline.com/doi/10.1080/0886022X.2024.2323160Anti-glomerular basement membrane diseaseIgA nephropathycrescentic glomerulonephritisimmunoglobulin Gprognosis
spellingShingle Zewei Chen
Dechao Xu
Fangzheng Cui
Huihui Hou
Zhiguo Mao
Xiang Gao
Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
Renal Failure
Anti-glomerular basement membrane disease
IgA nephropathy
crescentic glomerulonephritis
immunoglobulin G
prognosis
title Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
title_full Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
title_fullStr Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
title_full_unstemmed Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
title_short Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
title_sort coexistence of anti glomerular basement membrane disease and iga nephropathy an illustrative case and comprehensive literature review
topic Anti-glomerular basement membrane disease
IgA nephropathy
crescentic glomerulonephritis
immunoglobulin G
prognosis
url https://www.tandfonline.com/doi/10.1080/0886022X.2024.2323160
work_keys_str_mv AT zeweichen coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview
AT dechaoxu coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview
AT fangzhengcui coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview
AT huihuihou coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview
AT zhiguomao coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview
AT xianggao coexistenceofantiglomerularbasementmembranediseaseandiganephropathyanillustrativecaseandcomprehensiveliteraturereview