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回肠横结肠吻合术后53年回肠盲袢内腺癌

Adenocarcinoma in a Blind Loop of the Ileum 53 Years After an Ileotransversostomy Procedure.

作者信息

Takei Ryohei, Onishi Ichiro, Zaimoku Ryosuke, Makita Naoki, Yagi Yasumichi, Kayahara Masato

机构信息

Department of Surgery, National Hospital Organization Kanazawa Medical Center, Kanazawa, Ishikawa, Japan.

出版信息

Am J Case Rep. 2018 Feb 6;19:133-136. doi: 10.12659/ajcr.907144.

DOI:10.12659/ajcr.907144
PMID:29402880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5810614/
Abstract

BACKGROUND Primary small bowel cancer is a rare malignancy; the common histopathological types are carcinoid and adenocarcinoma. Inflammatory bowel diseases and familial adenomatous polyposis are known risk factors for small bowel cancer. Additionally, cases of surgery-induced small bowel adenocarcinoma are sometimes reported after ileostomy. CASE REPORT A 84-year-old woman, who had undergone ileotransversostomy for intestinal obstruction due to postoperative adhesion following appendectomy at the age of 31 years, was referred to our hospital for further examination after experiencing abdominal pain in the right lower quadrant for 2 weeks. Laboratory data showed elevated serum levels of carcinoembryonic antigen (CEA, 102.9 ng/ml) and carbohydrate antigen 19-9 (CA19-9, 104 U/ml). Enhanced computed tomography (CT) revealed a 10-cm mass in the terminal ileum and a distention of the ileum and colon in the blind loop, with retention of feces. The patient was suspected of having ileal cancer by preoperative examination; therefore, right hemicolectomy with en bloc resection was performed. The tumor was histopathologically diagnosed as a well-differentiated and mucinous adenocarcinoma of the ileum. At over 12 months after surgery, tumor recurrence had not been observed. CONCLUSIONS Difficulties in diagnosis can cause delays in treatment and lead to poor prognosis, mainly because tumors in the small bowel rarely cause clinical symptoms. Adenocarcinoma of the ileum should be considered in postoperative patients with ileotransversostomy.

摘要

背景 原发性小肠癌是一种罕见的恶性肿瘤;常见的组织病理学类型为类癌和腺癌。炎症性肠病和家族性腺瘤性息肉病是已知的小肠癌危险因素。此外,回肠造口术后有时会报告手术诱发的小肠腺癌病例。病例报告 一名84岁女性,31岁时因阑尾切除术后粘连导致肠梗阻而接受了回肠横结肠造口术,在右下腹痛2周后被转诊至我院进行进一步检查。实验室数据显示血清癌胚抗原(CEA,102.9 ng/ml)和糖类抗原19-9(CA19-9,104 U/ml)水平升高。增强计算机断层扫描(CT)显示回肠末端有一个10厘米的肿块,盲袢处回肠和结肠扩张,伴有粪便潴留。术前检查怀疑该患者患有回肠癌;因此,进行了根治性右半结肠切除术。肿瘤经组织病理学诊断为回肠高分化黏液腺癌。术后12个月以上未观察到肿瘤复发。结论 诊断困难会导致治疗延误并导致预后不良,主要是因为小肠肿瘤很少引起临床症状。回肠横结肠造口术后患者应考虑回肠腺癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/5f277112408b/amjcaserep-19-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/25573c87e979/amjcaserep-19-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/6cd2ea5c2450/amjcaserep-19-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/5f277112408b/amjcaserep-19-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/25573c87e979/amjcaserep-19-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/6cd2ea5c2450/amjcaserep-19-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b9/5810614/5f277112408b/amjcaserep-19-133-g003.jpg

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