Diagnostic Reassessment of a Historical Case of Atypical Heparin-Induced Thrombocytopenia: Between Spontaneous Heparin-Induced Thrombocytopenia and a Vaccine-Induced Immune Thrombotic Thrombocytopenia-Like Syndrome

PF4-dependent disorders encompass a heterogeneous group of immune-mediated thrombotic syndromes, including heparin-induced thrombocytopenia (HIT), its autoimmune variants such as spontaneous HIT, and vaccine-induced immune thrombotic thrombocytopenia (VITT). The recent identification of VITT and VIT...

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Principais autores:	Jordan Wimmer, Solène Kirscher, Manon Dolt, Agathe Herb, Léa Pierre, Lélia Grunebaum, Olivier Feugeas, Laurent Sattler, Dominique Desprez
格式:	Artigo
語言:	Inglês
出版:	MDPI AG 2025-11-01
叢編:	Life
主題:	autoimmune heparin-induced thrombocytopenia PF4-disorders spontaneous heparin-induced thrombocytopenia VITT-like syndrome cerebral venous sinus thrombosis
在線閱讀:	https://www.mdpi.com/2075-1729/15/11/1767
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