Laugier-Hunziker syndrome: an important differential diagnosis for Peutz-Jeghers syndrome. J Med Genet 2003;40:e77.Lampe AK,Hampton PJ,Woodford-Richens K,et al.Laugier-Hunziker syndrome:an important differential diagnosis for Peutz-Jeghers syndrome[J].J Med Genet,2003,40(6):77....
pigmentation varying in color from bluish black to dark brown to blue; lesions may fade over time Differential diagnosis Familial adenomatous polyposis; Cowden disease; juvenile polyposis; Ruvalcaba-Myhre-Smith; Turcot syndrome; Carney's syndrome; Cronkhite-Canada syndrome Therapy No treatment for mucocu...
STK11 adnexal tumor is a novel malignant neoplasm of uncertain histogenesis frequently arising in a para-adnexal location and associated with Peutz-Jeghers syndrome in 50% of patients. Its broad morphologic spectrum and nonspecific immunohistochemical profile has resulted in misclassification in the past ...
pigmentation varying in color from bluish black to dark brown to blue; lesions may fade over time Differential diagnosis Familial adenomatous polyposis; Cowden disease; juvenile polyposis; Ruvalcaba-Myhre-Smith; Turcot syndrome; Carney's syndrome; Cronkhite-Canada syndrome Therapy No treatment for mucocu...
MCCUSICK (Peutz-Jeghers syndrome), Dr. GORLIN (LEOPARD syndrome), Dr. CARNEY (Carney complex). This represents a unique blend of clinical and basic ... Alan S. Penzias,R Gobbelé,TD Waberski,... - 《Hormone & Metabolic Research》 被引量: 68发表: 1998年 ...
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
This combination can be so impressive that the diagnosis of Peutz-Jeghers syndrome since its first description more than 80 years ago could be regarded as a ?diagnosis at a glance". The genetic defect underlying the Peutz-Jeghers syndrome has been discovered 4 years ago. Since 1998 molecular ...
Given the clinical presentation, endoscopic and histopathological findings, a diagnosis of Peutz-Jeghers syndrome (PJS) was made.Hammad,H.T.Division of Gastroenterology 1 Hospital DriveColumbia MO United StatesFrazier,S.R.Division of Gastroenterology 1 Hospital DriveColumbia MO United StatesHolly,J.S....
Laugier-Hunziker syndromePeutz-Jeghers syndromeOral pigmentation is seen fairly commonly in dermatologic practice. Oral pigmentation associated with Laugier-Hunziker syndrome (LHS) is an uncommon condition that shares some dermatologic features with Peutz-Jeghers syndrome (PJS). It is benign and ...
Peutz-Jeghers syndromeSTK11 geneMutationGynecological cancerSummaryBackground: Peutz-Jeghers syndrome (PJS), a rare hereditary disorder, is characterized by the occurrence of gastrointestinal hamartomatous polyps associated with mucocutaneous pigmentation. Patients are at an increased cancer risk not only for...