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家族性腺瘤性息肉病外科手术方式的选择 被引量:2
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作者 程应东 罗云生 单志堂 《临床外科杂志》 2000年第2期81-83,共3页
目的 探讨家族性腺瘤性息肉病 (FAP)手术方式的选择和效果。方法 对 17例 FAP的临床资料进行回顾性分析。结果  17例病人中良性 13例 ,癌变 4例。全部病人均施行了全结肠切除 ,采用回肠造口 1例 ,回直肠吻合 2例 ,直肠切除、回肠肛... 目的 探讨家族性腺瘤性息肉病 (FAP)手术方式的选择和效果。方法 对 17例 FAP的临床资料进行回顾性分析。结果  17例病人中良性 13例 ,癌变 4例。全部病人均施行了全结肠切除 ,采用回肠造口 1例 ,回直肠吻合 2例 ,直肠切除、回肠肛管吻合或回肠储袋、回肠肛管吻合 7例 ,部分直肠切除、直肠粘膜剥脱经直肠肌鞘回肠肛管吻合 7例。并发症 2例 (肠坏死 1例 ,吻合口瘘 1例 )。随访 2~ 2 0年 ,良性病人术后均存活 ,其中 2例发生储袋炎 ,1例术后 5年发生癌变。4例癌变病人中 2例因广泛转移死亡 ,另 2例仍存活。排便功能以回肠造口术较差 ,保留直肠的术式较好。结论 比较各种术式的利弊 ,选择全结肠切除 ,保留直肠肌鞘 ,回肠储袋 。 展开更多
关键词 家族 腺瘤性息肉瘤 外科手术 结肠切除
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家族性腺瘤性息肉病研究进展
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作者 张建铎 马法运 《医学综述》 1999年第8期364-365,共2页
家族性腺瘤性息肉病(Familial adenomatouspo-lyposis,FAP)乃常染色体显性遗传性疾病。该病外显率高,并有极高的结肠癌发病率。本文拟对FAP及其几种变异体的临床特点、遗传学、筛检方法、治疗等最新研究进展进行简要综述。
关键词 家族 腺瘤性息肉瘤 临床特点 遗传学
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家族性腺瘤性息肉病8例报告 被引量:1
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作者 钱井华 邵桂清 《中国综合临床》 北大核心 2001年第2期122-122,共1页
目的探讨家族性腺瘤性息肉病的病因、临床特征及治疗。方法结合文献进行分析经治疗的 8例家族性腺瘤性息肉病。结果 8例中 5例有明确的家族史 ,均有慢性腹泻史、便血。病变均侵及直肠 ,行手术治疗 ,术后随访 1~ 10年 ,均健在。结论本... 目的探讨家族性腺瘤性息肉病的病因、临床特征及治疗。方法结合文献进行分析经治疗的 8例家族性腺瘤性息肉病。结果 8例中 5例有明确的家族史 ,均有慢性腹泻史、便血。病变均侵及直肠 ,行手术治疗 ,术后随访 1~ 10年 ,均健在。结论本病是一种常染色体显性遗传性综合征。凡可疑本病者 。 展开更多
关键词 腺瘤性息肉瘤 遗传 家族 肠肿瘤 诊断 治疗 外科手术
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Serrated neoplasia of the colorectum 被引量:4
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作者 Nathan T Harvey Andrew Ruszkiewicz 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第28期3792-3798,共7页
Serrated polyps of the colorectum form a group of related lesions which include aberrant crypt foci (ACF), conventional hyperplastic polyps, mixed (admixed) polyps, serrated adenomas and sessile serrated adenomas. In ... Serrated polyps of the colorectum form a group of related lesions which include aberrant crypt foci (ACF), conventional hyperplastic polyps, mixed (admixed) polyps, serrated adenomas and sessile serrated adenomas. In recent years the molecular differences between these morphologically similar lesions have been highlighted, and their differing biological potential has been realised. In particular, the sessile serrated adenoma has become recognised as the precursor lesion to a group of sporadic colorectal carcinomas characterised by morphological and molecular features distinct from conventional adenomas. These recent findings have challenged the long held paradigm that all colorectal carcinomas arise via the traditional adenoma-carcinoma sequence. In addition, they present a major challenge for the early detection and management of colorectal cancer, which is no longer regarded as a homogeneous entity. 展开更多
关键词 Serrated adenoma Serrated neoplasia Serrated adenocarcinoma Hyperplastic polyps Microsatellite instability
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Gardner's syndrome:Genetic testing and colonoscopy are indicated in adolescents and young adults with cranial osteomas:A case report 被引量:7
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作者 Dubravko Smud Goran Augustin +3 位作者 Tihomir Kekez Emil Kinda Mate Majerovic Zeljko Jelincic 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第28期3900-3903,共4页
We present a case of a 25-year-old female with diagnosed familial adenomatous polyposis and elevated carcinoembryonic antigen with negative family history. The suspicion of Gardner's syndrome was raised because ex... We present a case of a 25-year-old female with diagnosed familial adenomatous polyposis and elevated carcinoembryonic antigen with negative family history. The suspicion of Gardner's syndrome was raised because extirpation of an osteoma of the left temporo-occipital region was made 10 years ago. Restorative procto-colectomy and ileal pouch anal anastomosis was made but histology delineated adenocarcinoma of the rectum (Dukes C stage). We conclude that cranial osteomas often precede gastrointestinal manifestations of familial adenomatous polyposis or Gardner's syndrome and such patients should be evaluated with genetic testing followed by colonoscopy if results are positive to prevent the development of colorectal carcinoma. If the diagnosis is positive all family members should be evaluated for familial adenomatous polyposis. 展开更多
关键词 Gardner's syndrome Familial adenomatous polyposis Restorative proctocolectomy Ileal pouch anal anastomosis Cranial osteoma
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