Delamarre J, Capron J P, Dupas J L, Descombes P, Lesage J P, Deschepper B
Service de Radiologie, Centre Hospitalier Universitaire Nord, Amiens.
Gastroenterol Clin Biol. 1988 Jun-Jul;12(6-7):579-82.
The authors report 3 cases of fundic gland polyposis associated with Gardner's syndrome. Control endoscopies revealed fundic gland polyposis disappearance 14, 14, and 7 years respectively after discovery, and colectomy performed at ages 29, 30, and 32, respectively. This regression, described in autonomous fundic gland polyposis, is poorly documented in Gardner's syndrome. This phenomenon is not related to colectomy. However no explanation is currently available, and further studies are necessary to determine the factors related to the natural history of fundic gland polyposis in familial adenomatosis coli/Gardner's syndrome.
作者报告了3例与加德纳综合征相关的胃底腺息肉病。对照内镜检查显示，胃底腺息肉分别在发现后14年、14年和7年消失，患者分别在29岁、30岁和32岁时接受了结肠切除术。这种在自主性胃底腺息肉病中出现的消退现象，在加德纳综合征中鲜有记录。这种现象与结肠切除术无关。然而，目前尚无解释，需要进一步研究以确定与家族性腺瘤性息肉病/加德纳综合征中胃底腺息肉病自然史相关的因素。
