Human herpesvirus‐8‐related Kaposi's sarcoma after liver transplantation successfully treated with cidofovir and liposomal daunorubicin

: The iatrogenic form of Kaposi's sarcoma (KS) is typically observed among transplant recipients, and the most appropriate therapeutic approach (usually including reduction of immunosuppression, specific chemotherapy, and/or administration of antiviral agents against human herpes virus‐8) is st...

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Vydané v:Transplant infectious disease Ročník 7; číslo 1; s. 34 - 37
Hlavní autori: Verucchi, G., Calza, L., Trevisani, F., Zambruni, A., Tadolini, M., Giuliani, R., Manfredi, R., Andreone, P., Chiodo, F., Bernardi, M.
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Oxford, UK Munksgaard International Publishers 01.03.2005
Predmet:
Antibiotics, Antineoplastic - therapeutic use
Antiviral Agents - therapeutic use
cidofovir
Cytosine - analogs & derivatives
Cytosine - therapeutic use
daunorubicin
Daunorubicin - therapeutic use
Drug Therapy, Combination
Herpesvirus 8, Human - isolation & purification
human herpes virus‐8
Humans
Immunocompromised Host
Kaposi's sarcoma
liver transplantation
Liver Transplantation - adverse effects
Male
Middle Aged
Organophosphonates - therapeutic use
Sarcoma, Kaposi - drug therapy
Sarcoma, Kaposi - virology
Viral Load
Viremia
ISSN:1398-2273, 1399-3062
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Popis
Shrnutí:: The iatrogenic form of Kaposi's sarcoma (KS) is typically observed among transplant recipients, and the most appropriate therapeutic approach (usually including reduction of immunosuppression, specific chemotherapy, and/or administration of antiviral agents against human herpes virus‐8) is still controversial. Available experiences on the effect of the anti‐herpes viruses drug cidofovir provide conflicting results. Herein, we report the clinical, histological, and virological features of a liver transplant recipient successfully treated with a combined therapy of cidofovir and liposomal daunorubicin, associated with a reduction of the immunosuppressive regimen, for an advanced cutaneous and visceral KS.
Bibliografia:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ObjectType-Report-1
ObjectType-Article-3
ISSN:1398-2273
1399-3062
DOI:10.1111/j.1399-3062.2005.00081.x