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- polyposis adenomatous 腺瘤性息肉病
- Objective To investigate the surgical treatment of familial adenomatous polyposis(FAP). 目的 探讨家族性腺瘤样息肉病 (familialadenomatouspolyposis ,FAP)的外科治疗。
- Severe dysplasia in children with familial adenomatous polyposis:Rare or simply overlooked? 家族性腺瘤样息肉病患儿的重度不典型增生:是否罕见或仅是被忽略
- As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant. 家族性腺瘤息肉病的遗传方式是常染色体显性遗传。
- The conditions were familial adenomatous polyposis, myotonic dystrophy, multiple endocrine neoplasia, hereditary motor and sensory neuropathy. 这些疾病包括家族腺瘤息肉
- Objective To assess the clinical efficacy of sulindac on familial adenomatous polyposis (FAP) and its possible mechanism. 目的 观察舒林酸对家族性腺瘤息肉病 (FAP)的临床疗效 ,并探讨其可能的作用机制。
- The APC gene was identified in 1991 at chromosome 5 q 21. which is responsible for the familial adenomatous polyposis (FAP). APC基因是1991年被发现的一类肿瘤抑制基因,它被定位于人第5号染色体5q21处。
- This is familial polyposis in which the mucosal surface of the colon is essentially a carpet of small adenomatous polyps. 图示的是家族性结肠息肉病，在乙状结肠的表面可见较多的小的息肉状腺瘤。
- Conclusion: Congenital hypertrophy of retinal pigment epithelium (CHRPE) associated with familiar adenomatous polyposis has been described before. 结论：家族性大肠肉症之肠胃道以外的临床表现，以视网膜色素上皮肥大为常见之病灶。
- Objective:To discuss the value of congenital hypertrophy retinal pigment epithelium(CHRPE) in diagnosis of familial adenomatous polyposis(FAP). 目的:探讨先天性视网膜色素上皮细胞肥大(CHRPE)在家族性腺瘤性息肉病诊断中的意义。
- However, adenomatous hyperplasia is premalignant. 但是腺瘤状内膜增生可进展为癌。
- Objective: To discuss the value of congenital hypertrophy retinal pigment epithelium (CHRPE) in diagnosis of familial adenomatous polyposis (FAP). 摘要目的：探讨先天性视网膜色素上皮细胞肥大(CHRPE)在家族性腺瘤性息肉病诊断中的意义。
- Here are multiple adenomatous polyps of the cecum. 盲肠的多发性腺瘤息肉。
- Familial adenomatous polyposis (FAP) is an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine. 什么是'家族性腺瘤性息肉-继承条件多生长在大肠癌'?
- The patient had a villous adenoma. 这个病人曾长过绒毛状腺瘤。
- Six cases were misdiagnosed as pleomorphic adenoma. 误诊以多形性腺瘤最多见,达6例。
- The authors reported their retrospective analysis of peri-operation n ursing of 8 patients with familial adenomatous polyposis after panproctocolectom y under abdominoscope. 笔者回顾分析8例家族性腺瘤性息肉病病人经腹腔镜下全结肠直肠切除术治疗的围手术期护理。
- Juvenile polyposis syndrome is a rare hamartomatous disorder. 摘要幼年型息肉症是很罕见的缺陷瘤。
- Objective To evaluate long term outcome of ileal pouch anal anastomosis(IPAA )and ileorectal anastomosis(IRA) in patients with familial adenomatous polyposis(FAP). 目的探讨家族性腺瘤性息肉病采用回肠贮袋肛管吻合术与回肠直肠吻合术两种术式的手术效果。
- All the cases were confirmed by histopathologic examination, including 13 cases of patients with single or multiple polyps and 10 cases of adenomatous polyposis. 全部病例均经病理组织学检查证实，伴单发或多发性息肉13例，其中腺瘤性息肉10例。
