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一名日本男性患者患腹腔疾病合并I型肠病相关T细胞淋巴瘤的病例。

A case of celiac disease with type I enteropathy-associated T-cell lymphoma in a Japanese male patient.

作者信息

Hiraga Hiroto, Sakuraba Hirotake, Tanaka Nahoko, Watanabe Rina, Akemoto Yui, Ota Shinji, Kikuchi Hidezumi, Sawaya Manabu, Hiraga Noriko, Chinda Daisuke, Hanabata Norihiro, Mikami Tatsuya, Shimoyama Tadashi, Takahata Takenori, Tanaka Masanori, Fukuda Shinsaku

机构信息

Department of Gastroenterology and Hematology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

Department of Medical Oncology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.

出版信息

Immunol Med. 2019 Sep;42(3):142-147. doi: 10.1080/25785826.2019.1673031. Epub 2019 Oct 11.

Abstract

A 45-year-old Japanese male patient who was diagnosed with celiac disease (CeD) developed type I enteropathy-associated T-cell lymphoma (EATL). In 2013, the patient was admitted to our hospital with worsening of diarrhea and weight loss. Pathological examination of biopsy specimens from the duodenum and ileum led to a diagnosis of suspected EATL. A previous total colonoscopy (TCS) indicated villous atrophy in the terminal ileum. The patient was changed to a gluten-free diet, and the nutritional status gradually improved. In September 2014, he experienced acute right lower abdominal pain. He underwent urgent surgery, and a perforation was identified in the ileum. A diagnosis of type I EATL was made following histopathological examination. After eight courses of CHOP therapy, the patient entered complete remission. TCS and esophagogastroduodenoscopy with magnifying narrow-band imaging performed in 2015 identified villous regrowth in the distal ileum and duodenum. Capsule endoscopy also found villous regrowth in the entire small intestine. To our knowledge, this is the first case of type I EATL following CeD with villous atrophy before EATL occurrence in a Japanese HLA-DQ2 carrier. The possibility of type I EATL occurring after CeD should be recognized, although CeD is quite rare in Japan.

摘要

一名45岁的日本男性患者被诊断为乳糜泻(CeD),随后发展为I型肠病相关T细胞淋巴瘤(EATL)。2013年,该患者因腹泻加重和体重减轻入住我院。十二指肠和回肠活检标本的病理检查结果诊断为疑似EATL。此前的全结肠镜检查(TCS)显示末端回肠有绒毛萎缩。患者改为无麸质饮食,营养状况逐渐改善。2014年9月,他出现急性右下腹疼痛。他接受了紧急手术,术中发现回肠穿孔。组织病理学检查后确诊为I型EATL。经过8个疗程的CHOP治疗后,患者进入完全缓解期。2015年进行的TCS以及带放大窄带成像的食管胃十二指肠镜检查发现远端回肠和十二指肠有绒毛再生。胶囊内镜检查也发现整个小肠有绒毛再生。据我们所知,这是日本首例HLA-DQ2携带者在发生EATL之前出现CeD伴绒毛萎缩后发生的I型EATL病例。尽管CeD在日本相当罕见,但仍应认识到CeD后发生I型EATL的可能性。

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