Secondary Hemophagocytic Lymphocytosis in Inflammatory Bowel Disease.

IF 1.1 Q4 HEMATOLOGY
Jacob Boccucci, Ramalakshmi Thulluri, Chandini Kannan, Matthew Gold, Vamsi Kota
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引用次数: 0

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.

炎性肠病的继发性噬血细胞淋巴细胞增多症。
背景和临床意义:嗜血球性淋巴组织细胞增多症(HLH)是一种罕见且危及生命的疾病,由于其与严重感染的重叠特征而常被误诊。虽然在炎症性肠病(IBD)中使用硫嘌呤与HLH有关,但这些患者中的大多数将并发eb病毒(EBV)感染。病例介绍:本报告提出了一个病例的HLH患者以前用氮杂硫嘌呤治疗IBD没有并发病毒感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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