Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, Michigan, USA.
Diagn Cytopathol. 2022 Aug;50(8):414-416. doi: 10.1002/dc.24999. Epub 2022 Jun 8.
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening syndrome of pathologic immune response characterized by excessive activation of macrophages. Hemophagocytosis is one of the diagnostic criteria for HLH, and it usually involves the bone marrow, spleen, lymph nodes, or any part of the reticuloendothelial system. Hemophagocytosis in the ascitic fluid has rarely been reported in HLH. Here, we report the case of a patient who presented with fever and abdominal distention and ascites. Ascitic fluid cytology showed hemophagocytosis which was the clue for HLH diagnosis. We also review the literature for this rare cytological occurrence.
噬血细胞性淋巴组织细胞增生症(HLH)是一种危及生命的病理性免疫反应综合征,其特征为巨噬细胞过度激活。噬血现象是 HLH 的诊断标准之一,通常涉及骨髓、脾脏、淋巴结或网状内皮系统的任何部位。HLH 很少在腹水液中出现噬血现象。在这里,我们报告了一例以发热、腹胀和腹水为表现的患者。腹水细胞学检查显示噬血现象,这是 HLH 诊断的线索。我们还对这一罕见的细胞学表现进行了文献复习。