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罕见的结肠印戒细胞癌模拟幼年息肉。

A rare case of a signet ring cell carcinoma of the colon mimicking a juvenile polyp.

机构信息

Department of Internal Medicine, Armed Forces Daejeon Hospital, Daejeon, Korea.

出版信息

Gut Liver. 2012 Jan;6(1):129-31. doi: 10.5009/gnl.2012.6.1.129. Epub 2012 Jan 12.

Abstract

Primary signet ring cell carcinoma (SRC) of colon at early stage is quite rare. Only 26 cases were reported until now. We report an early stage of primary SRC which was misdiagnosed as a juvenile polyp and treated with polypectomy followed by surgical resection. A 21-year-old male was administered for hematochezia. Abdominopelvic enhanced computed tomography revealed a polyp with active bleeding at the proximal rectum just below the rectosigmoid junction. Colonoscopy examination revealed a colon polyp with 0.5 cm sized head. Polypectomy was performed with snare and the polyp was completely removed. Biopsy revealed SRC. Surgical resection was also performed and there were no residual tumor or lymph node metastasis in the surgical specimen.

摘要

早期结肠原发性印戒细胞癌(SRC)非常罕见。到目前为止,仅报告了 26 例。我们报告了一例早期原发性 SRC,该病例最初被误诊为幼年性息肉,并接受息肉切除术,随后进行了外科切除术。一名 21 岁男性因便血就诊。腹部盆腔增强 CT 显示直肠乙状结肠交界处近端直肠有一活动性出血的息肉。结肠镜检查发现一个 0.5cm 大小的息肉头。采用圈套器进行息肉切除术,息肉完全切除。活检显示 SRC。也进行了外科切除术,手术标本中无肿瘤残留或淋巴结转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9310/3286732/1147a1727859/gnl-6-129-g001.jpg

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