碰撞性腺癌-溃疡性结肠炎引起的直肠类癌

Nobuyoshi Yamazaki , Yuji Nishizawa , Motohiro Kojima , Nobuhiro Sugano , Akihiro Kobayashi , Masaaki Ito , Norio Saito
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引用次数: 0

摘要

溃疡性结肠炎(UC)致直肠碰撞性类癌1例。患者为78岁男性,直肠肿瘤,70岁时被诊断为UC。经内镜诊断为深粘膜下浸润性直肠癌。患者行经肛门局部切除术。苏木精-伊红染色切片病理检查显示两种不同的组织学类型:一种是常规的粘膜下浸润的高分化管状腺癌,另一种是由细胞核均匀的小细胞和呈小梁状排列的嗜酸性颗粒状细胞质组成。免疫组织化学染色显示,这些细胞嗜铬粒蛋白A和CD56阳性。这些细胞Ki-67指数低于2%,有丝分裂低于1/10 HPF。这些地区有明显的边界。因此,考虑该肿瘤为碰撞癌-类癌。最终,患者在局部切除2年后因复发死亡。由溃疡性结肠炎引起的碰撞癌-类癌肿瘤极为罕见。总的来说,我们认为碰撞瘤的行为是相对具有侵略性的。更仔细地监测结直肠碰撞或复合癌-类癌肿瘤是必要的,即使是在早期或类癌很小的时候。
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Collision adenocarcinoma–carcinoid tumor of the rectum arising in ulcerative colitis

A case of a collision carcinoma–carcinoid tumor of the rectum that arose in ulcerative colitis (UC). The patient was a 78-year-old man with a rectal tumor, who was diagnosed as having UC at 70 years of age. The tumor was diagnosed by endoscopy as a deep submucosal invasive rectal carcinoma. The patient underwent trans-anal local excision. Pathological examination of Hematoxylin–Eosin stained slides showed two different histological types: a conventional well differentiated tubular adenocarcinoma with submucosal invasion, and another that was composed of small cells with uniform nuclei and eosinophilic granular cytoplasm arranged in a trabecular pattern. Immnohistochemically, these cells were positive for chromogranin A and CD56. These cells exhibited a Ki-67 index that was less than 2% and mitosis in less than 1/10 HPF. These areas showed clear margins. Therefore, this tumor was considered to be a collision carcinoma–carcinoid tumor. Ultimately, the patient died 2 years after the local excision due to recurrence. Collision carcinoma–carcinoid tumors arising in ulcerative colitis are extremely rare. Collectively, it is considered that the behavior of the collision tumor is relatively aggressive. More careful surveillance of colorectal collision or composite carcinoma–carcinoid tumors is necessary, even when the carcinoma is early stage or the carcinoid is small.

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