التفاصيل البيبلوغرافية
العنوان:
A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene
المؤلفون:
M. Vernez , O. Gugerli , N. Halkic , P. Hutter , Hanifa Bouzourene , C. Monnerat
المصدر:
Familial Cancer, vol. 6, no. 1, pp. 141-145
سنة النشر:
2006
مصطلحات موضوعية:
Adenoma , Adult , Cancer Research , Pathology , medicine.medical_specialty , Skin Neoplasms , Proline , Sebaceous Gland Neoplasm , DNA Mutational Analysis , Mutation, Missense , Cholangiocarcinoma , Neoplasms, Multiple Primary , Germline mutation , Polyps , Muir–Torre syndrome , Neoplastic Syndromes, Hereditary , Genetics , medicine , Serine , Missense mutation , Humans , Sebaceous Gland Neoplasms , Genetics (clinical) , Intrahepatic Cholangiocarcinoma , Germ-Line Mutation , business.industry , Brain Neoplasms , Carcinoma , Liver Neoplasms , Syndrome , medicine.disease , Adenocarcinoma, Mucinous , Colorectal Neoplasms, Hereditary Nonpolyposis , Adenocarcinoma, Mucinous/genetics , Adenocarcinoma, Mucinous/surgery , Adenoma/genetics , Adenoma/surgery , Brain Neoplasms/genetics , Brain Neoplasms/secondary , Carcinoma/genetics , Carcinoma/surgery , Cholangiocarcinoma/genetics , Cholangiocarcinoma/secondary , Colorectal Neoplasms, Hereditary Nonpolyposis/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/surgery , DNA Probes , DNA-Binding Proteins , Endometrial Neoplasms/surgery , Female , Liver Neoplasms/genetics , Liver Neoplasms/surgery , Microsatellite Instability , MutS Homolog 2 Protein/deficiency , Neoplasms, Multiple Primary/genetics , Neoplasms, Multiple Primary/surgery , Neoplastic Syndromes, Hereditary/genetics , Neoplastic Syndromes, Hereditary/surgery , Polyps/surgery , Proline/genetics , Sebaceous Gland Neoplasms/genetics , Sebaceous Gland Neoplasms/surgery , Serine/genetics , Skin Neoplasms/genetics , Skin Neoplasms/secondary , digestive system diseases , Endometrial Neoplasms , MutS Homolog 2 Protein , Oncology , MSH2 , Cancer research , Adenocarcinoma , business
الوصف:
Muir-Torre syndrome (MTS) is a rare cancer-predisposing syndrome that is autosomal dominantly inherited and characterized by the development of sebaceous skin lesions (adenomas, epitheliomas, basaliomas and carcinomas). These lesions are typically associated with tumors that belong to the spectrum of hereditary nonpolyposis colorectal cancer (HNPCC) (i.e., tumors of the colorectum, endometrium, stomach or ovary). Biliary malignancy in association with MTS has only rarely been reported. We report a case of Muir-Torre syndrome associated with intrahepatic cholangiocarcinoma, a location not previously described, and associated with a novel missense mutation of the MSH2 gene (c.2026T > C), predicted to disrupt the function of the gene.
وصف الملف:
application/pdf
تدمد:
1389-9600
URL الوصول:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5938883bf5826766a13f0d7e2e2601 https://pubmed.ncbi.nlm.nih.gov/17051350
حقوق:
OPEN
رقم الأكسشن:
edsair.doi.dedup.....5e5938883bf5826766a13f0d7e2e2601
قاعدة البيانات:
OpenAIRE
