ArticleCureus2026
Adult Primary Hemophagocytic Lymphohistiocytosis (HLH) Initially Suspected as Brucellosis-Associated HLH: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome. Due to overlapping symptoms, primary HLH can be challenging to distinguish from brucellosis-associated HLH. This report describes the case of a 40-year-old male farmer who presented with progressive pancytopenia, body aches, fatigue, anorexia, weight loss, and fever. Laboratory examination showed severe leukopenia, anemia, thrombocytopenia, and abnormal liver function tests. Serology was positive for
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Registered trials
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