HHV8-Positive Multicentric Castleman's Disease and Thrombotic Thrombocytopenic Purpura among HIV-Positive Patients.

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Date publication

février 2024

Journal

European journal of case reports in internal medicine

Auteurs

Membres identifiés du Cancéropôle Est :
Dr NICOLAE Alina


Tous les auteurs :
Pasquer R, Dieudonné Y, Decours P, Hinschberger O, Nicolae A, Martinot M

Résumé

Castleman's disease (CD) and thrombotic thrombocytopenic purpura (TTP) are rare diseases that can affect the general population, especially those with HIV. Owing to their rarity, the association between CD and TTP remains insufficiently understood. In this study, we present a case of a 53-year-old patient with controlled HIV infection who presented with fever, lymphadenopathy, severe anaemia, and thrombocytopenia. After a series of tests, the diagnosis was concurrent human herpesvirus 8 (HHV8)-related multicentric CD (MCD) and TTP. Only four male patients were previously reported having this association, with HHV8 present in four and HIV in three patients, suggesting that coinfection with HHV8 and HIV is a pivotal factor in MCD with TTP occurrence.

Mots clés

Castleman’s disease, HHV8, HIV, autoimmune hypoglycaemia, thrombotic thrombocytopenic purpura

Référence

Eur J Case Rep Intern Med. 2024 02 28;11(3):004361