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Atypical acquired hemophilia linked with primary biliary cholangitis: a unique case presentation

Acquired hemophilia A is an uncommon disease often presented with bleeding episodes causing a significant mortality risk. The main responsible for the threatening hemorrhagic disorder is the Factor VIII autoantibody’s development. Acquired inhibitors’ presence is frequently idiopathic, but it can be...

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Principais autores: Fatma Megdiche, Nour Siala, Faten Kallel, Imen Krichen, Hend Hachicha, Imen Frikha, Maha Charfi, Naourez Kallel, Moez Medhaffar, Hatem Masmoudi, Moez Elloumi, Choumous Kallel
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis Group 2025-12-01
Serier:Future Science OA
Fag:
Acquired hemophilia A
activated partial thromboplastin time
autoimmune diseases
FVIII inhibitor
hemorrhage
primary biliary cholangitis
Online adgang:https://www.tandfonline.com/doi/10.1080/20565623.2025.2489329
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