Peutz-Jeghers相关论文
BACKGROUND Peutz-Jeghers syndrome(PJS)is a genetic disorder characterized by the development of gastrointestinal hamarto......
病例报告男，２４岁．缘于４岁时发现口唇有密集黑色素斑点，５岁时被家人发现在排便中肛门外有脱出物，经当地检查为息肉，未引起重视．成年后反复出现......
1 病例报告患儿女 ,13岁。因反复下腹痛 2年加剧 3天入院。两年来患儿常因饱食后诱发中下腹阵发性疼痛 ,能自行缓解 ,偶伴呕吐 ,......
Peutz-Jeghers综合征(PJS)是一种常染色体显性遗传病,现行的临床诊断条件为消化道2个或2个以上经组织学证实的错构瘤性息肉、皮肤......
目的检测Hedgehog信号通路中SHH蛋白及其下游转录因子GLI1蛋白在人Peutz-Jeghers综合征(PJS)息肉中的表达,探讨其在PJS发生及恶变......
目的:检测新疆地区口周色素沉着-肠道息肉综合征(PJS)2个家系6例患者及3例散发患者外周血及息肉组织致病基因STK11的突变,探讨新疆......
1 临床资料、患者女,9岁,因面黄、头晕、乏力一月于1992年12月14日入院。患者出生时发现小唇有一米粒大小的棕黑色色素斑,后缓慢......
目的 探讨Peutz-Jeghers综合征2个家系及3例散发病例外周血及息肉组织STK11基因的突变.方法 PCR扩增STK11基因前8个外显子及侧翼序......
Solitary Peutz-Jeghers type hamartomatous polyp is rare.It is considered to be related to a variant PeutzJeghers syndrom......
AIM: To investigate multiple polyps in a Chinese PeutzJeghers syndrome（PJS） infant. METHODS: A nine-month-old PJS infant w......
Peutz-Jeghers syndrome(PJS)is an inherited,autosomal dominant disorder distinguished by hamartomatous polyps in the gast......
Peutz-Jeghers syndrome(PJS) is a rare, autosomal dominant disease linked to a mutation of the STK 11 gene and is charact......
Laparoscopic restorative proctocolectomy with ileal pouch-anal anastomosis for Peutz-Jeghers syndrom
We report on a patient diagnosed with PeutzJeghers syndrome(PJS) with synchronous rectal cancer who was treated with lap......
AIM:To explore mutations in serine/threonine kinase 11(STK11) gene in Peutz-Jeghers syndrome(PJS) with gastrointestinal(......
AIM: To assess the usefulness of the balloon assisted enteroscopy in preventing surgical intervention in pa-tients with ......
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by the development of hamartomatous polypos......
Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by gastrointestinal hamarto......
目的探讨LKB1在Peutz-Jeghers综合征（PJS）错构瘤及肠上皮细胞中对上皮间质转化（EMT）调控作用。方法采用免疫组化法检测20例PJS错构瘤标......
目的通过经肛充气灌肠法探究多层螺旋CT对黑斑-息肉综合征(Peutz-Jeghers syndrome,PJS)患者小肠病变的检出率及其临床价值。方法......
Endoscopic snare papillectomy for a solitary Peutz-Jegherstypepolyp in the duodenum with ingrowth in
Solitary duodenal Peutz-Jeghers （PJ）-type hamartomatouspolyps are rare and considered a differentdisease entity than class......
Must Peutz-Jeghers syndrome patients have the LKB1/STK11 gene mutation?A case report and review of t
Peutz-Jeghers syndrome(PJS)is an autosomal dominant inherited disease,which is characterized by mucocutaneous pigmentati......
患者女性,43岁,经期延长3年,下腹疼痛1个月,于2018年8月入院。体检:患者嘴唇、四肢可见散在黑斑。子宫颈轻度糜烂,触血阳性。患者......
BACKGROUND Peutz-Jeghers syndrome(PJS) is an autosomal dominant inherited disease easily causing secondary malignant cha......
1病例报告患者(先证者)女,18岁.因口周及双侧指端众多点状黑斑,并渐增多而于2001年2月24日就诊.患者出生后不久先于上口唇出现散在......
BACKGROUND Peutz-Jeghers syndrome(PJS)is a rare disease with clinical manifestations of pigmented spots on the lips,muco......
BACKGROUND Peutz-Jeghers syndrome(PJS) and mesenteric fibromatosis(MF) are rare diseases,and PJS accompanying MF has not......
黑斑息肉综合征(Peutz-Jeghers syndrome,PJS)又称皮肤及黏膜黑色素斑-胃肠道息肉病综合征,是一种以皮肤及黏膜色素沉着、胃肠道多......
期刊
Colorectal cancer （CRC） is a major cause of morbidityand mortality around the world, and approximately 5%of them develop i......
<正>Peutz-Jeghers综合征(Peutz-Jeghers’s syndrome,PJS)又称黑斑息肉病,是常染色体显性遗传。1921年,Peutz第一个描述此综合征,......
<正>患者男,19岁,主因口周黑色素沉着19年,加重4年,发现结肠息肉3个月拟行内镜下电切于2008年4月3日入院。患者自幼口周及手掌、脚......
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<正>患者,男,2005年(18岁)在我院参加高考体检时,我科参检医生见其嘴唇及指间有斑点样色素沉着建议其行胃肠镜检查。高考结束后,患......
