Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis.

IgG4-related renal disease acute kidney injury case report kidney biopsy retroperitoneal fibrosis

Journal

Translational andrology and urology
ISSN: 2223-4691
Titre abrégé: Transl Androl Urol
Pays: China
ID NLM: 101581119

Informations de publication

Date de publication:
Apr 2020
Historique:
entrez: 19 5 2020
pubmed: 19 5 2020
medline: 19 5 2020
Statut: ppublish

Résumé

A 51-year-old woman visited our clinic for orthopnea, chest discomfort, and facial and leg edema. Acute kidney injury and pleural effusion were diagnosed and she received hemodialysis. This is a rare case of IgG4-related disease diagnosed by renal biopsy in the patient with retroperitoneal fibrosis and severe acute kidney injury, which progressed rapidly and required hemodialysis without markedly elevated serum IgG4 level and urinary tract obstruction. Immunostaining of a kidney biopsy revealed IgG4-related renal disease and magnetic resonance imaging showed retroperitoneal fibrosis in the paraspinal and presacral areas. After 3 days of glucocorticoid treatment, renal function and bilateral pleural effusion were restored. Another 2 months of glucocorticoid treatment decreased the extent of retroperitoneal fibrosis on follow-up abdominal computed tomography. IgG4-related disease is a recently recognized fibro-inflammatory condition with a dense lymphoplasmacytic infiltration of IgG4-positive plasma cells. The kidney and retroperitoneum are the frequently associated organs in IgG4-related disease. This case shows that IgG4-related disease can involve the kidney and/or other organs and be diagnosed by kidney biopsy.

Identifiants

pubmed: 32420186
doi: 10.21037/tau.2020.02.06
pii: tau-09-02-794
pmc: PMC7215037
doi:

Types de publication

Case Reports

Langues

eng

Pagination

794-799

Informations de copyright

2020 Translational Andrology and Urology. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau.2020.02.06). The authors have no conflicts of interest to declare.

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Auteurs

Young Jin Kim (YJ)

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea.

Ga-Eon Kim (GE)

Department of Pathology, Chonnam National University Medical School, Gwangju, South Korea.

Seong Kwon Ma (SK)

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea.

Soo Wan Kim (SW)

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea.

Eun Hui Bae (EH)

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea.

Classifications MeSH