نتایج جستجو برای: myxoma carney complex multiple endocrine neoplasia

تعداد نتایج: 1529822  

Journal: :Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2014
Eniko Havrankova Emoke Stenova Ingrid Olejarova Katarina Sollarova Sona Kinova

Cardiac myxomas make up approximately 50% of all benign cardiac tumors and represented 86% of all surgically treated cardiac tumors. Most of them originated from the left atrium, in some cases from both of atria. We report a case of male patient with biatrial myxomas and other extra-cardiac involvement: hypophyseal adenoma, enlargement of thyroid gland, tubular adenoma polyp of colon and bilate...

Journal: :The Journal of clinical endocrinology and metabolism 2006
A F Daly M-L Jaffrain-Rea A Ciccarelli H Valdes-Socin V Rohmer G Tamburrano C Borson-Chazot B Estour E Ciccarelli T Brue P Ferolla P Emy A Colao E De Menis P Lecomte F Penfornis B Delemer J Bertherat J L Wémeau W De Herder F Archambeaud A Stevenaert A Calender A Murat F Cavagnini A Beckers

CONTEXT Familial pituitary adenomas occur rarely in the absence of multiple endocrine neoplasia type 1 (MEN1) and Carney complex (CNC). OBJECTIVE Our objective was to characterize the clinical and genealogical features of non-MEN1/CNC familial isolated pituitary adenomas (FIPA). DESIGN AND SETTING We conducted a retrospective study of clinical and genealogical characteristics of FIPA cases ...

Journal: :World Journal of Endocrine Surgery 2014

Journal: :Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion 2011
Eladio José Losada Grande Daniel Al Kassam Martínez Margarita González Boillos

Carney complex (CNC) is an autosomal dominantly inherited syndrome characterized by spotty skin pigmentation, cardiac and cutaneous myxoma, and endocrine overactivity. Skin pigmentation includes lentigines and blue nevi. Myxomas may occur in breast, skin and heart. Cardiac myxomas may be multiple and occur in any cardiac chamber, and are more prone to recurrence. The most common endocrine gland...

2017
Sung Joon Han Woosik Han Min-Woong Kang Jae Hyeon Yu Shinkwang Kang Myung Hoon Na

Herein, we report on a family with Carney complex. Four members of the family underwent a total of 11 open heart operations as well as 9 other operations to treat extrathoracic masses. All the family members met at least 2 major clinical criteria and 1 supplemental criterion. We analyzed their genomic loci, including the protein kinase A regulatory subunit 1 gene. The results revealed no specif...

Journal: :Australian and New Zealand Journal of Medicine 2000

Journal: :Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2003
Jun Amano Tetsuya Kono Yuko Wada Tianshu Zhang Naohiko Koide Minoru Fujimori Ken-ichi Ito

Cardiac myxoma is most common among primary cardiac tumors, and its origin and tumor characteristics have been gradually elucidated by recent advances in molecular biology. Prichard's structure in the interatrial septum which was reported to be a candidate for the origin of cardiac myxoma, was revealed to be age-related changes. In hereditary cardiac myxoma "Carney complex", chromosomal abnorma...

Journal: :The Journal of clinical endocrinology and metabolism 1999
C A Stratakis J A Carney L S Kirschner H S Willenberg S Brauer M Ehrhart-Bornstein S R Bornstein

Carney complex (CNC) is characterized by lentiginosis and myxomatosis together with a variety of endocrine, neural crest-derived, and other tumors, including primary pigmented nodular adrenocortical disease (PPNAD). PPNAD is characterized by lipofuscin-containing, autonomously functioning, cortisol-producing nodules surrounded by mostly atrophic adrenocortical and normal adrenomedullary tissue....

2014
Shweta Birla Sameer Aggarwal Arundhati Sharma Nikhil Tandon

UNLABELLED Carney complex (CNC) is a rare autosomal dominant syndrome characterized by pigmented lesions of the skin and mucosae along with cardiac, endocrine, cutaneous, and neural myxomatous tumors. Mutations in the PRKAR1A gene have been identified in ∼70% of the CNC cases reported worldwide. A 30-year-old male was referred to the endocrinology clinic with suspected acromegaly. He had a hist...

2012
Luis V. Syro Bernd W. Scheithauer Kalman Kovacs Rodrigo A. Toledo Francisco J. Londoño Leon D. Ortiz Fabio Rotondo Eva Horvath Humberto Uribe

We briefly review the characteristics of pituitary tumors associated with multiple endocrine neoplasia type 1. Multiple endocrine neoplasia type 1 is an autosomal-dominant disorder most commonly characterized by tumors of the pituitary, parathyroid, endocrine-gastrointestinal tract, and pancreas. A MEDLINE search for all available publications regarding multiple endocrine neoplasia type 1 and p...

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