黑斑息肉综合征(Peutz-Jeghers syndrome, PJS)又称家族性黏膜皮肤色素沉着胃肠道息肉病,是一种常染色体显性遗传病,以皮肤黏膜色素沉着、胃肠道多发息肉为主要特点。患病率为1/200000~1/8000。患者胃肠道息肉发生癌变风险较高,需要定期监测、规律随诊、及时治疗。黑斑息肉综合征是一种常染色体显性遗传疾病,大部分与...
The meaning of PEUTZ-JEGHERS SYNDROME is a familial polyposis inherited as an autosomal dominant trait and characterized by numerous polyps in the stomach, small intestine, and colon and by melanin-containing spots on the skin and mucous membranes especi
消化道多发性息肉综合征(Peutz-Jeghers Syndrome)本综合征是指在唇部和颊部粘膜出现色素斑点合并有胃肠息肉并有家族史.这是一种特殊疾患,早已为人们所熟悉.色素斑:在皮肤及粘膜出现0.5~10毫米大,棕色或蓝棕色,圆形或不规则形,境界明显的色素斑.本综合征不可缺少的及在诊断上有价值的是发生在唇红部和颊部的色素...
#手术室日常 #医学科普 黑斑息肉综合征(Peutz-Jeghers syndrome, PJS)又称家族性黏膜皮肤色素沉着胃肠道息肉病,是一种常染色体显性遗传病,以皮肤黏膜色素沉着、胃肠道多发息肉为主要特点。患病率为1/200000~1 - 青岛妇儿任医生于20211011发布在抖音,已经收获了17.3万
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波伊茨-耶格综合征(Peutz-Jeghers syndrome,PJS),也被称为黑斑息肉综合征,是常染色体显性遗传的综合征,是一类伴有黏膜、皮肤色素沉着的全胃肠道多发性息肉病。2018年5月该疾病被列入国家卫生健康委员会等5部门联合制定的《第一批罕见病目录》。 PJS发病率约 1...
Peutz-Jeghers SyndromeHereditary hamartosis Peutz-Jeghers; Hutchinson–Weber–Peutz syndrome; Lentiginosis polyposa Peutz; Peutz–Touraine syndrome; PJS Peutz–Jeghers syndrome is an autosomal dominantly inherited...doi:10.1007/978-3-642-16483-5_4482Tilman VogelBritish Journal of Cancer...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by melanotic macules, intestinal polyps, and an increased cancer risk. It is caused by mutations in the serine/threonine kinase 11 gene (LKB1, STK11). About 1 in 100,000 ind
网络黑斑息肉综合征;黑斑息肉病 网络释义
Cancer and the Peutz-Jeghers syndrome. Among 72 patients with the Peutz-Jeghers syndrome malignant tumours have developed in 16 (22%) of whom all but one have died. There were nine gastrointesti... AD Spigelman,V Murday,RK Phillips - Gut 被引量: 1745发表: 0年 Feminizing sex cord tumor...