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Cited by 414

The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.

How I treat hemophagocytic lymphohistiocytosis in the adult patient

Open access
Schram, Alison M., Berliner, Nancy·2015·Blood

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a devastating disorder of uncontrolled immune activation characterized by clinical and laboratory evidence of extreme inflammation. This syndrome can be caused by genetic mutations affecting cytotoxic function (familial HLH) or be secondary to infectious, rheumatologic, malignant, or metabolic conditions (acquired HLH). Prompt recognition is paramount and, without early treatment, this disorder is frequently fatal. Although HLH is well described in the pediatric population, less is known about the appropriate work-up and treatment in adults. Here, we review the clinical characteristics, diagnosis, and treatment of HLH in adults.

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Metadata

Authors
Schram, A. M., & Berliner, N.
Venue
Blood
Published
2015-05-07
Volume
125
Issue
19
Pages
2908-2914
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2068646465
Cited by
414
References
70
FWCI
21.48
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: How I treat hemophagocytic lymphohistiocytosis in the adult patient. https://app.cochat.ai/papers/10.1182/blood-2015-01-551622
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Schram, A. M., & Berliner, N. (2015). How I treat hemophagocytic lymphohistiocytosis in the adult patient. Blood. https://doi.org/10.1182/blood-2015-01-551622

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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