Indolent peripheral T-cell lymphoma resembling Kimura's disease: a new variant of T-cell Lymphoma?

IF 0.9 Q4 HEMATOLOGY
Hui Sun , Jia Feng , Yaping Zhang , Jianguo Zhang , Shaolei Lu , Yifei Liu
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引用次数: 0

Abstract

Kimura's disease (KD) is a rare chronic inflammatory disorder of unknown etiology prevalent in middle-aged Asian males. Kimura's disease transforming to T-cell lymphoma or coexisting with T-cell lymphoma have not been reported in the scientific literature except two cases of Kimura's disease resembling peripheral T-cell lymphoma morphologically. There was no corresponding entity included in the current WHO classification (5th ed., 2022). It might be a new variant of peripheral T-cell lymphoma. Here, we present the first reported case of coexisting KD and indolent peripheral T-cell lymphoma in a 55-year-old Chinese man.
类似木村病的惰性外周t细胞淋巴瘤:一种新的t细胞淋巴瘤变体?
木村病(KD)是一种罕见的慢性炎症性疾病,病因不明,常见于亚洲中年男性。木村病转化为t细胞淋巴瘤或与t细胞淋巴瘤共存,除两例形态学上类似外周t细胞淋巴瘤的木村病外,尚未见科学文献报道。目前的世卫组织分类(第5版,2022年)中没有相应的实体。它可能是一种新的外周t细胞淋巴瘤。在这里,我们报告了一例55岁的中国男性并发KD和惰性外周t细胞淋巴瘤的病例。
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
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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