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非特指的肠道 T 细胞淋巴瘤,表现为息肉样病变:一例报告。

Intestinal T-cell lymphomas NOS presenting as a polypoidal lesion: A case report.

机构信息

The Second People's Hospital of Shaanxi Province, Xi'an, Shaanxi Province, China.

出版信息

Medicine (Baltimore). 2024 Jun 7;103(23):e38465. doi: 10.1097/MD.0000000000038465.

DOI:10.1097/MD.0000000000038465
PMID:38847694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11155561/
Abstract

RATIONALE

Intestinal T-cell lymphomas are exceedingly rare diseases. Intestinal T-cell lymphoma NOS, as a "wastebasket" category, is difficult to diagnosis. Endoscopy can identify abnormal mucosa in most patients at a reasonably early stage. Therefore, it is crucial to increase the understanding of endoscopists in terms of the endoscopic characteristics of ITCL.

PATIENT CONCERNS

A 74-year-old male alone with wasting as the major complaint, had multiple polypoid lesions in the large intestine. The patient then had endoscopic care.

DIAGNOSES

Only 1 polypoid lesion on white-light endoscopy in the sigmoid colon was pathologically diagnosed as intestinal T-cell lymphomas, not otherwise specified (ITCL-NOS).

INTERVENTIONS

The patient underwent intensity-reduced CHOP therapy.

OUTCOMES

The patient is still with controlled disease but developed chemotherapy-related side effects.

LESSONS

In the individual with unexplained anemia and waste, endoscopy should not be delayed. For each of polypoid lesion on white-light endoscopy, the endoscopist need to remain cautious, because every lesion in the same patient can exhibit the independence of histopathological features. Meanwhile, we suggest that endoscopists should routinely observe the terminal ileum, even take biopsy samples if necessary.

摘要

背景

肠 T 细胞淋巴瘤是极为罕见的疾病。肠 T 细胞淋巴瘤非特指型作为一个“分类垃圾桶”,诊断困难。内镜检查可使大多数患者在相当早的阶段发现异常黏膜。因此,提高内镜医生对 ITCL 内镜特征的认识至关重要。

患者关注

一名 74 岁男性,因消瘦为主诉,大肠内有多个息肉样病变。患者随后进行了内镜检查。

诊断

乙状结肠白光内镜下仅发现 1 个息肉样病变,经病理诊断为肠 T 细胞淋巴瘤,非特指型(ITCL-NOS)。

干预

患者接受了强度降低的 CHOP 治疗。

结果

患者疾病仍处于控制中,但出现了化疗相关的副作用。

教训

对于原因不明的贫血和消瘦患者,不应延迟进行内镜检查。对于白光内镜下的每个息肉样病变,内镜医生都需要保持警惕,因为同一患者的每个病变都可能表现出独立的组织病理学特征。同时,我们建议内镜医生应常规观察末端回肠,如果必要,还应进行活检取样。

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本文引用的文献

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Endoscopic and Histopathological Characteristics of Gastrointestinal Lymphoma: A Multicentric Study.胃肠道淋巴瘤的内镜及组织病理学特征:一项多中心研究
Diagnostics (Basel). 2023 Aug 26;13(17):2767. doi: 10.3390/diagnostics13172767.
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Update on the Pathogenesis of Enteropathy-Associated T-Cell Lymphoma.肠病相关T细胞淋巴瘤发病机制的最新进展
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Clinical and Histopathological Features of an Italian Monocentric Series of Primary Small Bowel T-Cell Lymphomas.
意大利单中心原发性小肠T细胞淋巴瘤系列病例的临床和组织病理学特征
Cancers (Basel). 2023 May 13;15(10):2743. doi: 10.3390/cancers15102743.
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Classification and challenges in the histopathological diagnosis of peripheral T-cell lymphomas, emphasis on the WHO-HAEM5 updates.外周T细胞淋巴瘤组织病理学诊断的分类与挑战,重点介绍世界卫生组织血液和淋巴组织肿瘤分类第5版更新内容
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CD30 + Primary intestinal T-cell lymphoma (unclassified) masquerading as chronic inflammation: a case report.CD30+原发性肠道 T 细胞淋巴瘤(未分类)伪装为慢性炎症:一例报告。
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Blood. 2022 Sep 15;140(11):1229-1253. doi: 10.1182/blood.2022015851.
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Targeted Next-generation Sequencing Reveals a Wide Morphologic and Immunophenotypic Spectrum of Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma.靶向下一代测序揭示了单一表型上皮嗜肠道 T 细胞淋巴瘤的广泛形态学和免疫表型谱。
Am J Surg Pathol. 2022 Sep 1;46(9):1207-1218. doi: 10.1097/PAS.0000000000001914. Epub 2022 May 12.
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