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克-特综合征中的结肠弥漫性海绵状血管瘤。

Diffuse cavernous hemangioma of the colon in the Klippel-Trenaunay syndrome.

作者信息

Ghahremani G G, Kangarloo H, Volberg F, Meyers M A

出版信息

Radiology. 1976 Mar;118(3):673-8. doi: 10.1148/118.3.673.

Abstract

Large, infiltrative cavernous hemangiomas of the distal colon were present in 3 children with the Klippel-Trenaunay syndrome, 2 of whom are the subject of this report. The lesion is manifested clinically as intermittent rectal bleeding starting in the first 5 years of life. The radiographic features include (a) varicose lesions in the wall of the rectosigmoid, ranging from a network of distended submucosal veins to nodular defects, (b) narrowing of the rectum by the surrounding extramural portion of the hemangioma, and (c) phleboliths within the lesion. Inferior mesenteric angiography and sigmoidoscopy are useful for preoperative confirmation. The occurrence of visceral hemangiomas in the Klippel-Trenaunay syndrome and its relevant diagnostic and therapeutic implications are discussed.

摘要

3例患有克-特综合征的儿童存在远端结肠的巨大浸润性海绵状血管瘤,其中2例为本报告的研究对象。该病变在临床上表现为生命最初5年内开始出现的间歇性直肠出血。影像学特征包括:(a)直肠乙状结肠壁上的静脉曲张病变,范围从扩张的黏膜下静脉网到结节状缺损;(b)血管瘤的周围壁外部分使直肠变窄;(c)病变内的静脉石。肠系膜下血管造影和乙状结肠镜检查有助于术前确诊。本文讨论了克-特综合征中内脏血管瘤的发生情况及其相关的诊断和治疗意义。

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