尸检
弥漫性血管内凝血
医学
噬血细胞性淋巴组织细胞增多症
骨髓
病理
病因学
全血细胞减少症
死因
不明原因发热
内科学
疾病
作者
Samirkuma Amin,Udit Naik,Wei Wang,Shaimaa Elzamly,Meenakshi B. Bhattacharjee
出处
期刊:PubMed
日期:2023-05-01
卷期号:53 (3): 489-493
摘要
Hemophagocytic lymphohistiocytosis (HLH) is an aggressive, life-threatening condition with sudden onset of a systemic inflammatory response syndrome. The triggers can be apparently non-specific, and the clinical presentations can be very deceptive during a rapidly deteriorating clinical course. Herein, we report a case of a 49-year-old White/Caucasian male with no known past medical history who presented with multi-organ failure, including liver, kidney, and bone marrow, along with disseminated intravascular coagulation. He had a high probability of HLH. Unfortunately, he died ten days after the initial presentation. At autopsy, the liver was necrotic and immunostains revealed diffuse positivity for HSV-1 & 2. The bone marrow was markedly hypocellular with phagocytes containing intact and fragmented red blood cells. There was also disseminated fungal infection involving almost all tissues. PCR, done on frozen tissue samples, revealed Aspergillus fumigatus. The rapid and fatal course of this patient illustrates the sometimes-aggressive course of HLH and the importance of autopsy examination in revealing the underlying etiology for this patient's death.
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