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原发性阑尾腺癌因肿瘤侵犯乙状结肠而出现便血。

Primary Appendiceal Adenocarcinoma Presenting with Hematochezia due to the Invading Tumor in the Sigmoid Colon.

作者信息

Suzuki Tatsuya, Yamamoto Yasuhiro, Torigoe Toshihiko, Mizukami Shoichiro, Shigehara Kengo

机构信息

Department of Surgery, Kobayashi Hospital, 4-2, Kita-3-Jonishi, Kitami, Hokkaido 090-8567, Japan.

Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, Hokkaido 060-8556, Japan.

出版信息

Case Rep Surg. 2020 Sep 7;2020:8833573. doi: 10.1155/2020/8833573. eCollection 2020.

Abstract

Primary appendiceal tumors are rare malignancies; some cases have been described to invade other organs, and this represents a very rare clinical condition. We report a case of appendiceal adenocarcinoma invading the sigmoid colon and a review of similar cases. A 69-year-old woman with complaints of hematochezia was admitted to the hospital. Colonoscopy revealed a tumor in the sigmoid colon, which was a well-differentiated tubular adenocarcinoma. A computed tomography scan showed an appendiceal mass that involved the sigmoid colon, suggesting an appendiceal cancer invading the sigmoid colon. Ileocecal resection with extended lymphadenectomy and en bloc resection of the sigmoid colon was performed. The appendiceal tumor involved the sigmoid colon and the terminal ileum. The ileocecal part which included the tumor and the involved sigmoid colon was resected in total. Macroscopic findings showed that the appendiceal tumor made a fistula with the sigmoid colon. Pathological examination revealed that the tumor was a well-differentiated tubular adenocarcinoma that invaded the sigmoid colon. The final pathological stage was T4bN0M0, stage IIC. The patient was discharged from the hospital uneventfully. She was alive without relapse after a 20-month follow-up. Although an appendiceal tumor invading the rectosigmoid region is rare, a preoperative diagnosis can be obtained that facilitates the planning of a suitable surgical procedure: en bloc resection of the ileocecal part and the rectosigmoid part.

摘要

原发性阑尾肿瘤是罕见的恶性肿瘤;已有一些病例被描述为侵犯其他器官,这是一种非常罕见的临床情况。我们报告一例阑尾腺癌侵犯乙状结肠的病例,并对类似病例进行综述。一名69岁有便血症状的女性入院。结肠镜检查发现乙状结肠有一个肿瘤,为高分化管状腺癌。计算机断层扫描显示阑尾有一个肿块累及乙状结肠,提示阑尾癌侵犯乙状结肠。进行了包括扩大淋巴结清扫的回盲部切除术和乙状结肠整块切除术。阑尾肿瘤累及乙状结肠和回肠末端。将包括肿瘤和受累乙状结肠的回盲部全部切除。大体检查发现阑尾肿瘤与乙状结肠形成瘘管。病理检查显示肿瘤为侵犯乙状结肠的高分化管状腺癌。最终病理分期为T4bN0M0,II C期。患者顺利出院。经过20个月的随访,她存活且无复发。尽管阑尾肿瘤侵犯直肠乙状结肠区域很罕见,但可以获得术前诊断,这有助于规划合适的手术方案:回盲部和直肠乙状结肠部分的整块切除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b4/7492942/421c6889d2e0/CRIS2020-8833573.001.jpg

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