| Literature DB >> 26512263 |
Hee Young Ju1, Che Ry Hong1, Sung Jin Kim1, Ji Won Lee1, Hyery Kim1, Hyoung Jin Kang1, Kyung Duk Park1, Hee Young Shin1, Jong-Hee Chae2, Ji Hoon Phi3, Jung-Eun Cheon4, Sung-Hye Park5, Hyo Seop Ahn1.
Abstract
Hemophagocytic lymphohistiocytosis (HLH) is characterized by fever, splenomegaly, jaundice, and pathologic findings of hemophagocytosis in bone marrow or other tissues such as the lymph nodes and liver. Pleocytosis, or the presence of elevated protein levels in cerebrospinal fluid, could be helpful in diagnosing HLH. However, the pathologic diagnosis of the brain is not included in the diagnostic criteria for this condition. In the present report, we describe the case of a patient diagnosed with HLH, in whom the brain pathology, but not the bone marrow pathology, showed hemophagocytosis. As the diagnosis of HLH is difficult in many cases, a high level of suspicion is required. Moreover, the pathologic diagnosis of organs other than the bone marrow, liver, and lymph nodes may be a useful alternative.Entities:
Keywords: Brain; Central nervous system; Hemophagocytic lymphohistiocytosis
Year: 2015 PMID: 26512263 PMCID: PMC4623456 DOI: 10.3345/kjp.2015.58.9.358
Source DB: PubMed Journal: Korean J Pediatr ISSN: 1738-1061