全血细胞减少症
肝脾肿大
医学
内脏利什曼病
儿科
利什曼病
养生
免疫学
骨髓
重症监护医学
外科
病理
疾病
作者
Aman Bansal,Akshita Gupta,Monica Gupta,Sayantan Mukherjee,Anita Tahlan
出处
期刊:Case Reports
[BMJ]
日期:2025-06-01
卷期号:18 (6): e266300-e266300
标识
DOI:10.1136/bcr-2025-266300
摘要
bodies with haemophagocytosis. Thereafter, the patient was prescribed liposomal amphotericin B, but unfortunately, he succumbed to the illness. This case reiterates that infection is a frequent trigger of sHLH. The diagnosis of primary HLH in adults should be considered only after excluding all putative infectious causes, particularly in tropical regions.
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