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一例胆管原发性结外NK/T细胞淋巴瘤(结外NK/T细胞淋巴瘤)尸检病例。

An autopsy case of primary extranodal NK/T cell lymphoma (extranodal NK/T-cell lymphoma) of the bile duct.

作者信息

Ito Hiroyuki, Hiraiwa Shin-Ichiro, Sugiyama Tomoko, Tajiri Takuma, Yamaji Yoko, Kaneko Motoki, Tsuda Shingo, Ichikawa Hitoshi, Nagata Junko, Kojima Seiichiro, Takashimizu Shinji, Shirai Takayuki, Watanabe Norihito

机构信息

Department of Gastroenterology, Tokai University Hachioji Hospital, Tokyo, Japan.

Department of Pathology, Tokai University Hachioji Hospital, Tokyo, Japan.

出版信息

Clin J Gastroenterol. 2019 Jun;12(3):209-212. doi: 10.1007/s12328-018-00931-1. Epub 2019 Jan 2.

DOI:10.1007/s12328-018-00931-1
PMID:30603836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6543026/
Abstract

We reported the case of a 50-year-old man diagnosed with extrinsic NK/T-cell lymphoma. He was initially diagnosed with locally advanced unresected pancreatic duct carcinoma and was treated with combination chemotherapy using gemcitabine and nabpaclitaxel. One month after treatment, he developed bleeding. Upper gastrointestinal endoscopy showed a deep ulcer lesion from the duodenal bulb to the inner wall of the descending section that was not observed before treatment. Coil embolization was performed, but the necrotic area widened after treatment; the patient died of disseminated intravascular coagulation after 1 week. Autopsy showed a soft white-tone lesion that extended from the ulcer wall to the gallbladder wall and around the intrahepatic bile duct. Lesions were also found in the spleen, lungs, kidney, and bone marrow, and immunohistochemistry confirmed extrinsic NK/T-cell lymphoma (extranodal NK/T-cell lymphoma, nasal type). In conclusion, histological diagnosis of NK/T-cell lymphoma is difficult at an early stage, and the clinical course often shows rapid tumor progression, particularly bleeding in the digestive organs or widespread perforation and penetration. NK/T-cell lymphoma should be ruled out in patients with bile duct and pancreatic tumors in whom tissue diagnosis via biopsy cannot be performed.

摘要

我们报告了一例50岁男性,被诊断为外周NK/T细胞淋巴瘤。他最初被诊断为局部晚期不可切除的胰腺导管癌,并接受了吉西他滨和白蛋白结合型紫杉醇联合化疗。治疗一个月后,他出现了出血症状。上消化道内镜检查显示,十二指肠球部至降部内壁有一个治疗前未观察到的深部溃疡病变。进行了线圈栓塞治疗,但治疗后坏死区域扩大;患者在1周后死于弥散性血管内凝血。尸检显示,有一个软质白色病变,从溃疡壁延伸至胆囊壁及肝内胆管周围。在脾脏、肺、肾和骨髓中也发现了病变,免疫组织化学证实为外周NK/T细胞淋巴瘤(结外NK/T细胞淋巴瘤,鼻型)。总之,NK/T细胞淋巴瘤的早期组织学诊断困难,临床病程常显示肿瘤进展迅速,尤其是消化器官出血或广泛穿孔和浸润。对于无法通过活检进行组织诊断的胆管和胰腺肿瘤患者,应排除NK/T细胞淋巴瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/eb79db4ed459/12328_2018_931_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/16311b1586de/12328_2018_931_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/e6552fe7540a/12328_2018_931_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/eb79db4ed459/12328_2018_931_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/16311b1586de/12328_2018_931_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/e6552fe7540a/12328_2018_931_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4d/6543026/eb79db4ed459/12328_2018_931_Fig3_HTML.jpg

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