{"title":"Peutz-Jeghers综合征的诊断和治疗进展","authors":"Quan-Li Zhu, Wei Wu, Peng Chen, Diarra mohamed Diaty","doi":"10.3760/CMA.J.ISSN.1008-6315.2019.04.019","DOIUrl":null,"url":null,"abstract":"Peutz-Jeghers syndrome (PJS) is a rare syndrome characterized by multiple polyps of gastrointestinal tract and black spots of mucosa.The etiology is unclear yet.The main clinical manifestations are digestive tract symptoms and pigmentation of skin and mucosa.The diagnosis mainly depends on clinical manifestations and auxiliary examinations.Multiple gastrointestinal polyps can often be found by endoscopy.Gene testing can often detect mutations of serine/threonine kinase 11 (STK11) or liver kinase B1 (LKB1), which has high diagnostic accuracy.At present, PJS is rarely reported, and there is still a lack of systematic understanding.This paper reviews the incidence, clinical manifestations, auxiliary examinations, diagnosis, treatment and progress of PJS. \n \n \nKey words: \nPeutz-Jeghers Syndrome; Diagnosis and treatment","PeriodicalId":10365,"journal":{"name":"中国综合临床","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Advances in the diagnosis and treatment of Peutz-Jeghers syndrome\",\"authors\":\"Quan-Li Zhu, Wei Wu, Peng Chen, Diarra mohamed Diaty\",\"doi\":\"10.3760/CMA.J.ISSN.1008-6315.2019.04.019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Peutz-Jeghers syndrome (PJS) is a rare syndrome characterized by multiple polyps of gastrointestinal tract and black spots of mucosa.The etiology is unclear yet.The main clinical manifestations are digestive tract symptoms and pigmentation of skin and mucosa.The diagnosis mainly depends on clinical manifestations and auxiliary examinations.Multiple gastrointestinal polyps can often be found by endoscopy.Gene testing can often detect mutations of serine/threonine kinase 11 (STK11) or liver kinase B1 (LKB1), which has high diagnostic accuracy.At present, PJS is rarely reported, and there is still a lack of systematic understanding.This paper reviews the incidence, clinical manifestations, auxiliary examinations, diagnosis, treatment and progress of PJS. \\n \\n \\nKey words: \\nPeutz-Jeghers Syndrome; Diagnosis and treatment\",\"PeriodicalId\":10365,\"journal\":{\"name\":\"中国综合临床\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中国综合临床\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1008-6315.2019.04.019\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国综合临床","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1008-6315.2019.04.019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Advances in the diagnosis and treatment of Peutz-Jeghers syndrome
Peutz-Jeghers syndrome (PJS) is a rare syndrome characterized by multiple polyps of gastrointestinal tract and black spots of mucosa.The etiology is unclear yet.The main clinical manifestations are digestive tract symptoms and pigmentation of skin and mucosa.The diagnosis mainly depends on clinical manifestations and auxiliary examinations.Multiple gastrointestinal polyps can often be found by endoscopy.Gene testing can often detect mutations of serine/threonine kinase 11 (STK11) or liver kinase B1 (LKB1), which has high diagnostic accuracy.At present, PJS is rarely reported, and there is still a lack of systematic understanding.This paper reviews the incidence, clinical manifestations, auxiliary examinations, diagnosis, treatment and progress of PJS.
Key words:
Peutz-Jeghers Syndrome; Diagnosis and treatment
期刊介绍:
Clinical Medicine of China is an academic journal organized by the Chinese Medical Association (CMA), which mainly publishes original research papers, reviews and commentaries in the field.
Clinical Medicine of China is a source journal of Peking University (2000 and 2004 editions), a core journal of Chinese science and technology, an academic journal of RCCSE China Core (Extended Edition), and has been published in Chemical Abstracts of the United States (CA), Abstracts Journal of Russia (AJ), Chinese Core Journals (Selection) Database, Chinese Science and Technology Materials Directory, Wanfang Database, China Academic Journal Database, JST Japan Science and Technology Agency Database (Japanese) (2018) and other databases.