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TIM-3 缺陷表现为两次非克隆相关的肠系膜和皮下脂膜炎样 T 细胞淋巴瘤和噬血细胞性淋巴组织细胞增生症。

TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosis.

机构信息

Center for Pediatrics and Adolescent Medicine, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Institute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

出版信息

Pediatr Blood Cancer. 2020 Jun;67(6):e28302. doi: 10.1002/pbc.28302. Epub 2020 Apr 14.

DOI:10.1002/pbc.28302
PMID:32285995
Abstract

This report offers novel clinical and diagnostic aspects of the association between germline mutations in HAVCR2 and subcutaneous panniculitis-like T-cell lymphoma (SPTCL). The patient presented with panniculitis-like T-cell lymphoma involving mesenteric fatty tissue associated with hemophagocytic lymphohistiocytosis (HLH). Five years later, he developed a clonally unrelated SPTCL and underwent hematopoietic stem cell transplantation. Retrospectively, he was found to carry germline mutations in HAVCR2 associated with reduced T-cell immunoglobulin mucin-3 (TIM-3) expression. We show that mesenteric fatty tissue localization of SPTCL can be the presenting manifestation of TIM-3 deficiency, that this condition predisposes to recurrent lymphoma, and that flow cytometry is a possible screening tool.

摘要

本报告提供了 HAVCR2 种系突变与皮下脂膜炎样 T 细胞淋巴瘤(SPTCL)之间关联的新的临床和诊断方面。该患者表现为累及肠系膜脂肪组织的脂膜炎样 T 细胞淋巴瘤,伴有噬血细胞性淋巴组织细胞增多症(HLH)。五年后,他发生了克隆性无关的 SPTCL,并接受了造血干细胞移植。回顾性分析发现,他携带与 T 细胞免疫球蛋白粘蛋白-3(TIM-3)表达降低相关的 HAVCR2 种系突变。我们表明,SPTCL 的肠系膜脂肪组织定位可能是 TIM-3 缺陷的首发表现,这种情况易发生复发性淋巴瘤,流式细胞术可能是一种筛查工具。

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