原发性肠系膜类癌。

Journal of the Korean Surgical Society Pub Date : 2013-02-01 Epub Date: 2013-01-29 DOI:10.4174/jkss.2013.84.2.114
In-Soo Park, Bong-Hyeon Kye, Hyun-Sil Kim, Hyung-Jin Kim, Hyeon-Min Cho, Changyoung Yoo, Seong Su Hwang
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引用次数: 18

摘要

虽然继发性肠系膜受累是常见的,但原发性肠系膜类癌非常罕见,据报道为40%至80%。当肿瘤大小大于2 cm时,远处转移率为80% ~ 90%。我们报告一例罕见的原发性肠系膜类癌,虽然体积较大,但表现为良性。患者到韩国天主教大学圣文森特医院就诊,腹部肿块明显增加。在剖腹手术中,发现一个包被良好的肿块,起源于靠近Treitz韧带的肠系膜,未见邻近器官侵犯或远处转移。肿块大小为8.2 × 7.3 cm,组织病理学表现为良性。随访11个月,患者无复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary mesenteric carcinoid tumor.

Primary mesenteric carcinoid tumor.

Primary mesenteric carcinoid tumor.

Primary mesenteric carcinoid tumor.

Primary mesenteric carcinoid tumor is very rare, although secondary mesenteric involvement is common, reported as 40% to 80%. And distant metastasis rate reported as 80% to 90%, when the size is larger than 2 cm. We present a case of very rare primary mesenteric carcinoid tumor showing benign character though large size. The patient visited St. Vincent's Hospital, The Catholic University of Korea with increasing palpable abdominal mass. At laparotomy, a well encapsulated mass arising from the mesentery near the ligament of Treitz was found without any adjacent organ invasion or distant metastasis. The mass was measured as 8.2 × 7.3 cm and histopathologically benign character. At 11 months of follow up, the patient was recurrence free.

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