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炎症性肠病中的继发性噬血细胞性淋巴细胞增多症。

Secondary Hemophagocytic Lymphocytosis in Inflammatory Bowel Disease.

作者信息

Boccucci Jacob, Thulluri Ramalakshmi, Kannan Chandini, Gold Matthew, Kota Vamsi

机构信息

Department of Medicine, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

出版信息

Hematol Rep. 2025 Jun 30;17(4):33. doi: 10.3390/hematolrep17040033.

Abstract

Background and Clinical Significance: Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening condition that can go underdiagnosed due to overlapping features with severe infections. While the use of thiopurine in inflammatory bowel disease (IBD) has been associated with HLH, the majority of these patients will have a concurrent Epstein-Barr virus (EBV) infection. Case Presentation: This report presents a case of HLH in a patient previously treated with aza-thioprine for IBD without concurrent viral infection.

摘要

背景与临床意义

噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见且危及生命的疾病,由于其与严重感染有重叠特征,可能会诊断不足。虽然在炎症性肠病(IBD)中使用硫唑嘌呤与HLH有关,但这些患者中的大多数会同时感染爱泼斯坦-巴尔病毒(EBV)。病例报告:本报告介绍了一例曾接受硫唑嘌呤治疗IBD但无并发病毒感染的HLH患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d897/12286110/d52181ca193f/hematolrep-17-00033-g001.jpg

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