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[加德纳综合征中的梗阻性尿路病。腹腔内硬纤维瘤]

[Obstructive uropathy in Gardner's syndrome. Intra-abdominal desmoid tumor].

作者信息

Olivier Gómez C M, Carballido Rodríguez J A

出版信息

Actas Urol Esp. 1989 Sep-Oct;13(5):329-38.

PMID:2688366
Abstract

Desmoid tumours are benign neoplasias manifesting themselves clinically as aggressive fibromatoses. They may be sited both in mesenteric and retroperitoneal fat. Owing to the great size they reach and to their local infiltrative character they occasionally lead to the development of intestinal occlusive syndromes and, in exceptional cases, to obstructive uropathy of the upper urinary tract. Their incidence of presentation in the general population is low, however they develop more frequently in patients suffering from colonic polyposis in the family and they form part of the extracolonic manifestations of Gardner's syndrome. In 1987 we treated a young patient, a genetic carrier of familiar colonic polyposis who had presented relapse of a previous desmoid. The location of the tumour in narrow pelvis made its clinical debut as a intestinal pseudo-occlusion and determined a bilateral ureteral obstruction and the formation of a major urinoma. The joint utilization of instrumental maneuvers and surgical approaches enabled us to solve the intestinal and urological commitment satisfactorily. We carry out an overall review and analyse the data published on the incidence, prognosis and treatment of obstructive uropathy in Gardner's syndrome. We also carry out an updating on the biology of the desmoid tumour.

摘要

硬纤维瘤是一种良性肿瘤,临床上表现为侵袭性纤维瘤病。它们可位于肠系膜和腹膜后脂肪中。由于其体积巨大且具有局部浸润性,它们偶尔会导致肠梗阻综合征的发生,在特殊情况下,还会导致上尿路梗阻性肾病。它们在普通人群中的发病率较低,但在患有家族性结肠息肉病的患者中更常见,并且是加德纳综合征的结肠外表现之一。1987年,我们治疗了一名年轻患者,他是家族性结肠息肉病的基因携带者,之前的硬纤维瘤复发。肿瘤位于狭窄骨盆,临床首发表现为肠道假性梗阻,并导致双侧输尿管梗阻和巨大尿瘤形成。器械操作和手术方法的联合应用使我们能够令人满意地解决肠道和泌尿系统问题。我们对加德纳综合征中梗阻性肾病的发病率、预后和治疗方面发表的数据进行了全面回顾和分析。我们还对硬纤维瘤的生物学进行了更新。

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