Langerhans cell histiocytosis complicated with hemophagocytic lymphohistiocytosis in a boy with a novel XIAP mutation: A case report

RATIONALE: X-linked lymphoproliferative syndromes (XLPs) are rare, yet often fatal primary immunodeficiency diseases, which rarely manifest as Langerhans cell histiocytosis (LCH) complicated with hemophagocytic lymphohistiocytosis (HLH). Clinical data of a case of XLP-2 manifesting as LCH complicate...

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Detalles Bibliográficos
Autores principales: Guo, Xia, Li, Qiang, Gao, Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221634/
https://www.ncbi.nlm.nih.gov/pubmed/30383659
http://dx.doi.org/10.1097/MD.0000000000013019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221634/
https://www.ncbi.nlm.nih.gov/pubmed/30383659
http://dx.doi.org/10.1097/MD.0000000000013019

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