A Case of Spontaneously Improving Secondary Hemophagocytic Lymphohistiocytosis in an Adult Associated with T-Cell Histiocyte-Rich Large B-Cell Lymphoma

Secondary hemophagocytic lymphohistiocytosis (HLH) in adults is a rare, often fatal syndrome characterized by widespread immune dysregulation. It is seen as a complication of infections, autoimmune diseases, and malignancies. Among the malignancy-related causes, aggressive T-cell or NK-cell neoplasm...

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Vydáno v:Case Rep Oncol Med
Hlavní autoři: Askin, Cyrus, Burris, Ashley, Layman, Clifton, Haney, Brian, Hall, Jordan
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi 2018
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5842713/
https://ncbi.nlm.nih.gov/pubmed/29682376
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/8069182
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