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...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Jordan Wimmer, Solène Kirscher, Manon Dolt, Agathe Herb, Léa Pierre, Lélia Grunebaum, Olivier Feugeas, Laurent Sattler, Dominique Desprez
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	MDPI AG 2025-11-01
Sarja:	Life
Aiheet:	autoimmune heparin-induced thrombocytopenia PF4-disorders spontaneous heparin-induced thrombocytopenia VITT-like syndrome cerebral venous sinus thrombosis
Linkit:	https://www.mdpi.com/2075-1729/15/11/1767
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