Case Report: Kaposi Sarcoma in Anti-Glomerular Basement Membrane Disease

<ns3:p>Anti-glomerular basement membrane (anti-GBM) disease is a rare and life-threatening autoimmune vasculitis characterized by rapidly progressive glomerulonephritis, with or without pulmonary hemorrhage. Its management requires aggressive immunosuppressive therapy, including corticosteroids, cyclophosphamide, and plasmapheresis. Kaposi sarcoma (KS) is a vascular neoplasm linked to human herpes virus 8 (HHV-8), most frequently seen in HIV-infected or iatrogenically immunosuppressed patients. We report the case of a 39-year-old man with anti-GBM vasculitis who developed cutaneous Kaposi sarcoma two months after initiation of immunosuppressive treatment. HHV-8–positive spindle cell proliferation was confirmed on skin biopsy. HIV testing was negative, and the lesions regressed following the tapering of corticosteroids and withdrawal of cyclophosphamide. This case highlights the importance of considering KS as a differential diagnosis in patients developing skin lesions under immunosuppressive therapy for autoimmune vasculitis.</ns3:p>

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Publication Details

Journal
F1000Research
Published
2025-09-08
DOI
https://doi.org/10.12688/f1000research.165476.1
Primary Topic
Viral-associated cancers and disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Case Report: Kaposi Sarcoma in Anti-Glomerular Basement Membrane Disease

D. Zellama, Sanda Mrabet, R. Guesmi, Raja Boukadida et al.
F1000Research
Viral-associated cancers and disorders
article

Case Report: Kaposi Sarcoma in Anti-Glomerular Basement Membrane Disease

D. Zellama, Sanda Mrabet, R. Guesmi, Raja Boukadida, Zohra Sassi Jalleli
article en

Abstract

<ns3:p>Anti-glomerular basement membrane (anti-GBM) disease is a rare and life-threatening autoimmune vasculitis characterized by rapidly progressive glomerulonephritis, with or without pulmonary hemorrhage. Its management requires aggressive immunosuppressive therapy, including corticosteroids, cyclophosphamide, and plasmapheresis. Kaposi sarcoma (KS) is a vascular neoplasm linked to human herpes virus 8 (HHV-8), most frequently seen in HIV-infected or iatrogenically immunosuppressed patients. We report the case of a 39-year-old man with anti-GBM vasculitis who developed cutaneous Kaposi sarcoma two months after initiation of immunosuppressive treatment. HHV-8–positive spindle cell proliferation was confirmed on skin biopsy. HIV testing was negative, and the lesions regressed following the tapering of corticosteroids and withdrawal of cyclophosphamide. This case highlights the importance of considering KS as a differential diagnosis in patients developing skin lesions under immunosuppressive therapy for autoimmune vasculitis.</ns3:p>

F1000ResearchVol. 14
Gazi Hastanesi (TR), Hôpital Sahloul (TN), University of Sousse (TN)
Openalex Percentile: Top 52%
Viral-associated cancers and disorders
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