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首页> 外文期刊>Journal of Gastrointestinal Oncology >Indolent T cell lymphoproliferative disorder of the gastrointestinal tract: an uncommon case with lymph node involvement and the classic Hodgkin’s lymphoma
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Indolent T cell lymphoproliferative disorder of the gastrointestinal tract: an uncommon case with lymph node involvement and the classic Hodgkin’s lymphoma

机译:嗜毒T细胞淋巴血管疾病的胃肠道:含淋巴结受累的罕见案例和经典的霍奇金淋巴瘤

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Here we describe an unusual case of an indolent CD8+ T-cell lymphoproliferative disorder in the gastrointestinal tract (ITCLD-GT) accompanied by neck lymph node infiltration and new onset of classic Hodgkin’s lymphoma after two years follow-up. Previously, this 42-year-old Asian man suffered from diarrhea and abdominal pain for two years. Intestinal biopsies showed a group of small to intermediate-sized lymphocytes which were monomorphic as well as arranged in a nodular pattern with no clear boundary and were diagnosed as ITCLD-GT. He did not receive chemotherapy or have any disease progression in the gastrointestinal tract (GIT) during the follow-up until a development of neck lymphadenopathy, which led to an eventual mixed cellularity type of Hodgkin’s lymphoma, one type of classic HL diagnosis. Interestingly, besides the Hodgkin’s cells, the same pathological T-cells in the GIT were present in the Hodgkin’s lymphoma lesions. These two pathological T cells in GIT and neck lymph node had the identical histopathological and molecular abnormalities that confirmed the abenteric distant infiltration of ITCLD-GT to the neck lymph node in this patient. This is the first case of ITCLD-GT that has a definite distant lymph node invasion. ITCLD-GT usually has a relatively good prognosis but patients with ITCLD-GT may have abenteric distant infiltration. Thus, long-term follow-up and further study of the underlying mechanisms of this process are necessary.
机译:在这里,我们描述了胃肠道(ITCLD-GT)中的惰性CD8 + T细胞淋巴抑制性疾病的一种不寻常的情况,伴随着颈部淋巴结渗透和经典霍奇金淋巴瘤的新发生后续随访。此前,这位42岁的亚洲男子患有腹泻和腹痛两年。肠道活组织检查显示一组小于中等大小的淋巴细胞,其是单体的,并且以透明边界的结节图案排列,并且被诊断为ITCLD-GT。他在随访期间没有收到化疗或在胃肠道(Git)中有任何疾病进展,直到颈部淋巴结发育,这导致了最终混合细胞类型的霍奇金淋巴瘤,一种经典HL诊断。有趣的是,除了霍奇金的细胞外,Git中的相同病理T细胞存在于霍奇金淋巴瘤病变中。 Git和颈淋巴结中的这两种病理T细胞具有相同的组织病理学和分子异常,其证实ITCLD-GT对该患者的颈部淋巴结的逐渐渗透。这是ITCLD-GT的第一种案例,具有明确的淋巴结入侵。 ITCLD-GT通常具有相对良好的预后,但ITCLD-GT的患者可能具有脑室距离渗透。因此,需要长期随访和进一步研究该过程的潜在机制。

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