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Coexisting BRAF-Mutated Langerhans Cell Histiocytosis and Primary Myelofibrosis with Shared JAK2 Mutation

Langerhans cell histiocytosis (LCH) is an infrequent disease, characterized by oligoclonal proliferation of immature myeloid-derived cells. However, the exact pathogenesis remains unknown. In rare cases, LCH is present in patients with concomitant myeloid proliferative neoplasms. Here, we describe a...

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Detalles Bibliográficos
Autores principales:	Holst, Johanne Marie, Enemark, Marie Beck, Plesner, Trine Lindhardt, Pedersen, Martin Bjerregaard, Ludvigsen, Maja, d'Amore, Francesco
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068553/ https://www.ncbi.nlm.nih.gov/pubmed/33953993 http://dx.doi.org/10.1155/2021/6623706

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