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Enteropathy associated T-cell lymphoma: A review of diagnostic findings and therapeutic strategies

机译:肠病相关的T细胞淋巴瘤:诊断结果和治疗策略的回顾

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摘要

Enteropathy associated T-cell lymphoma (EATL) is an uncommon type of non-Hodgkin T-cell lymphoma of the intestinal intraepithelial T lymphocytes. Frequently presenting as intestinal perforation, ulceration, or a mass in the jejunum and proximal ileum in the gastrointestinal tract, EATL carries a poor prognosis with absence of well-defined therapeutic protocols for management. The WHO recognizes two distinct variants of EATL, the type I/classical variant and type II/monomorphic variant, based on different clinical features and histopathologic findings. EATL type I has a higher incidence in geographic regions with a high prevalence of celiac disease such as Northern Europe and is rare in the Asian population, in whom celiac disease is also rare. EATL type II can occur sporadically, has a higher incidence in Asian populations, with no definite association with celiac disease. This review aims to summarize the clinicopathologic findings of EATL and current approaches to management.
机译:肠病相关的T细胞淋巴瘤(EATL)是肠道上皮内T淋巴细胞的一种罕见的非霍奇金T细胞淋巴瘤。 EATL常表现为肠穿孔,溃疡或胃肠道空肠和回肠近端肿块,预后较差,缺乏明确的治疗方案。根据不同的临床特征和组织病理学发现,WHO可以识别EATL的两个不同变体,即I型/经典变体和II型/单态变体。 I型EATL在腹腔疾病流行率较高的地理区域(例如北欧)中发病率较高,在亚洲人群中很少见,在亚洲人群中腹腔疾病也很罕见。 EATL II型可以偶发发生,在亚洲人群中发病率较高,与乳糜泻没有明确的关联。这篇综述旨在总结EATL的临床病理学发现和当前的治疗方法。

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