| Literature DB >> 22729341 |
Zehra Pinar Koç1, Saadet Akarsu, Tansel Balci, Kemal Unal.
Abstract
Haemophagocytic lymphohistiocytosis (HLH) is a rare immune disorder that predominantly affects macrophages and T lymphocytes and leads to multiple organ disease and death. The characteristic pathological finding in the bone marrow and the other affected tissues is haemophagocytosis of macrophages (macrophages digesting erythrocyte). Primary (hereditary) and secondary (acquired) forms of the disease are present. A patient with documented HLH disease revealed by positron emission tomography/CT is reported in this paper.Entities:
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Year: 2012 PMID: 22729341 PMCID: PMC4542497 DOI: 10.1136/bcr-03-2012-6026
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X