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- Keywords Dacryon polyposis;Relevant factors;Incidence rate; 泪点息肉;患病率;相关因素;
- Dacryon polyposis 泪点息肉
- Juvenile polyposis syndrome is a rare hamartomatous disorder. 摘要幼年型息肉症是很罕见的缺陷瘤。
- Colonic carcinomas arising in patients with familial polyposis of the colon are frequently multiple. 家族性息肉症患者发生的结肠癌常常是多发的。
- Diagnosis revealed the presence of fundic gland polyps which suggested gastric polyposis in the fundus and body. 胃有无数小型、半圆，颜色如同正常黏膜密布于胃底及胃体的胃腺体息肉。
- 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
- Peutz-Jeghers, also known as Hereditary Intestinal Polyposis Syndrome, is an autosomal dominant genetic disease. 什么是'黑斑息肉综合征-多生长在肠道'?
- 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。
- Result:Adenocarcinoma, polyposis and angioma that did not be found before operation existed in abdomen of the patients. 方法:对31例剖腹术中不明确肠道病灶部位的患者介入纤维内镜寻找;
- Here is another example of polyposis with numerous small polyps covering the colonic mucosa. 息肉病，结肠黏膜覆盖有很多小息肉。
- The characteristics of gastric polyps and familial polyposis coli were reviewed carefully. 本文中并研讨此两种息肉症的关连及临床意义。
- After ESS, 77.7% of our chronic sinusitis patients with or without polyposis felt they had improved. 接受内视镜鼻窦手术后，77.;7%25的慢性鼻窦炎病患不管合并或不合并鼻息肉觉得他们的鼻窦炎症状有改善。
- 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
- Definition: Multiple pigmented( melanin) macules of the skin and mouth mucosa and multiple polyposis of the small intestine. 遗传性胃肠道息肉病伴粘膜皮肤色素沉着征，或简称黑斑-息肉综合征。指胃肠道有散在息肉，息肉较大，而且可有蒂及分叶状；同时皮肤粘膜有多发性黑色素痣，罕见疾病。
- When this mucus blanket is altered in amount or composition, rhinorrhea, nasal obstruction, polyposis, and sinusitis may develop. 当粘液层发生质或量的改变时，可导致鼻塞、鼻息肉、鼻窦炎等疾病症状。
- Purpose:To study the early molecular pathological changes in 14 adenomas of 10 familial adenomatous polyposis (FAP)patients. 目的 :研究来自 10个家族性多发性肠息肉症 (FAP)患者 14个腺瘤的早期分子病理学变化。
- 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。
