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Leukocytoclastic vasculitis caused by hepatitis C virus in a liver transplant recipient: A case report
Gustavo de Sousa Arantes Ferreira1, Andre Luis Conde Watanabe1, Natalia de Carvalho Trevizoli2
1Department of Liver Transplantation, Instituto de Cardiologia do Distrito Federal, Brasilia 70673-900, Brazil.
Insights
Leukocytoclastic vasculitis can be the initial sign of hepatitis C virus (HCV) recurrence post-liver transplant. Prompt antiviral treatment resolved skin symptoms, underscoring the importance of early diagnosis in immunosuppressed patients.
Area of Science:
- Hepatology
- Immunology
- Dermatology
Background:
- Hepatitis C virus (HCV) infection is a global health concern affecting the liver and potentially other organs, including the skin.
- Leukocytoclastic vasculitis is a known dermatologic manifestation of HCV, but its presentation as the first symptom of post-transplant HCV recurrence is undocumented.
Observation:
- A liver transplant recipient on immunosuppression developed palpable purpura on the lower extremities.
- Investigations revealed anemia, hypocomplementemia, ascites, bowel wall thickening, and pleural effusion. Skin biopsy confirmed leukocytoclasia; liver biopsy indicated HCV recurrence (genotype 1A).
Findings:
- HCV recurrence was confirmed with viral load of 11460 copies/mL.
- Treatment with ribavirin, sofosbuvir, and daclatasvir for 12 weeks led to rapid symptom regression and complete resolution.
Implications:
- This case highlights diagnostic challenges of HCV-related skin lesions in immunosuppressed transplant recipients.
- Early diagnosis and treatment of HCV recurrence are crucial for managing extrahepatic manifestations.
Background:
Infection by the hepatitis C virus (HCV) is currently considered to be a global health issue, with a high worldwide prevalence and causing chronic disease in afflicted individuals. The disease largely involves the liver but it can affect other organs, including the skin. While leukocytoclastic vasculitis has been reported as one of the dermatologic manifestations of HCV infection, there are no reports of this condition as the first symptom of HCV recurrence after liver transplantation.
Case Summary:
We report here a case of leukocytoclastic vasculitis in a liver transplant recipient on maintenance immunosuppression. The condition presented as a palpable purpura in both lower extremities. Blood and urine cultures were negative and all biochemical tests were normal, excepting evidence of anemia and hypocomplementemia. Imaging examination by computed tomography showed a small volume of ascites, diffuse thickening of bowel walls, and a small bilateral pleural effusion. Skin biopsy showed leukocytoclasia and fibrinoid necrosis. Liver biopsy was suggestive of HCV recurrence in the graft, and HCV polymerase chain reaction yielded 11460 copies/mL and identified the genotype as 1A. Treatment of the virus with a 12-wk direct-acting antiviral regimen of ribavirin, sofosbuvir and daclatasvir led to regression of the symptoms within the first 10 d and subsequent complete resolution of the symptoms.
Conclusion:
This case highlights the difficulties of diagnosing skin lesions caused by HCV infection in immunosuppressed patients.
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