Concurrent hepatitis B infection and IgA nephropathy in a patient with a history of malignant melanoma

IgA nephropathy (IgAN) is an immune complex-mediated glomerulonephritis characterized by the deposition of IgA-dominant immune complexes in the mesangium, leading to mesangial proliferation and subsequent renal injury. Clinically, IgAN often manifests as episodic macroscopic hematuria following upper respiratory tract or gastrointestinal infections. Disease progression is variable, with 20–50% of patients advancing to end-stage renal disease within 10–20 years of diagnosis. Although IgAN is primarily idiopathic, it may also occur secondary to systemic conditions such as Henoch-Schönlein purpura, HIV infection, toxoplasmosis, ankylosing spondylitis, and liver cirrhosis. Less commonly, IgAN can be associated with hepatitis B virus (HBV) infection or manifest as a paraneoplastic phenomenon. Here, we report a unique case of clinical presentation and successful treatment of concurrent HBV infection and IgAN in a patient with a history of malignant melanoma. To our knowledge, this is the first documented case in which these three conditions (IgAN, HBV infection, and malignant melanoma) coexist in a single patient.

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Publication Details

Journal
Ukrainian Journal of Nephrology and Dialysis
Published
2025-01-22
DOI
https://doi.org/10.31450/ukrjnd.1(85).2025.01
Primary Topic
Polyomavirus and related diseases
Type
article
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article

Concurrent hepatitis B infection and IgA nephropathy in a patient with a history of malignant melanoma

Alper Alp, Bülent Huddam, Ferda Bacaksızlar Sarı, Dilek Gibyeli Genek et al.
Ukrainian Journal of Nephrology and Dialysis
Polyomavirus and related diseases
article

Concurrent hepatitis B infection and IgA nephropathy in a patient with a history of malignant melanoma

Alper Alp, Bülent Huddam, Ferda Bacaksızlar Sarı, Dilek Gibyeli Genek, Mürşide Gülay ÖRGÜN SÖNMEZ, Gülsüm Ceren Terzioğlu
article en

Abstract

IgA nephropathy (IgAN) is an immune complex-mediated glomerulonephritis characterized by the deposition of IgA-dominant immune complexes in the mesangium, leading to mesangial proliferation and subsequent renal injury. Clinically, IgAN often manifests as episodic macroscopic hematuria following upper respiratory tract or gastrointestinal infections. Disease progression is variable, with 20–50% of patients advancing to end-stage renal disease within 10–20 years of diagnosis. Although IgAN is primarily idiopathic, it may also occur secondary to systemic conditions such as Henoch-Schönlein purpura, HIV infection, toxoplasmosis, ankylosing spondylitis, and liver cirrhosis. Less commonly, IgAN can be associated with hepatitis B virus (HBV) infection or manifest as a paraneoplastic phenomenon. Here, we report a unique case of clinical presentation and successful treatment of concurrent HBV infection and IgAN in a patient with a history of malignant melanoma. To our knowledge, this is the first documented case in which these three conditions (IgAN, HBV infection, and malignant melanoma) coexist in a single patient.

Ukrainian Journal of Nephrology and Dialysis(1(85))
Muğla University (TR)
Openalex Percentile: Top 94%
Polyomavirus and related diseases
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