نتایج جستجو برای: myxoma carney complex multiple endocrine neoplasia

تعداد نتایج: 1529822  

2016
Shohei Kataoka Masato Otsuka Masayuki Goto Mitsuru Kahata Asako Kumagai Koji Inoue Hiroshi Koganei Kenji Enta Yasuhiro Ishii

Cardiac tumors are rare, and multiple myxomas are even rarer. The latter phenomenon is mostly associated with the Carney complex, a dominantly inherited disease characterized by multiple primary cardiac myxomas, endocrinopathy, and spotty pigmentation of the skin. We report the rare case of a patient who did not have the Carney complex but had multiple primary cardiac tumors. A 78-year-old woma...

Journal: :Journal of clinical pathology 1997
L Masmiquel M Castro-Forns I de Torres A García M T Vidal R Simó

The aim was to evaluate Leu-M1 immunoreactivity as a prognostic factor in phaeochromocytoma. Anti-Leu-M1 monoclonal antibodies were used to determine the Leu-M1 immunoreactivity in 17 histologically confirmed phaeochromocytomas from 15 patients, using an avidin-biotin technique. Ten patients had a sporadic phaeochromocytoma, and five had multiple endocrine neoplasia type 2A (MEN 2A). Malignancy...

Journal: :Dicle Medical Journal / Dicle Tip Dergisi 2012

2014
C. Yuste M. Rapalai B.A. Pritchard T.J. Jones B. Tucker S.B. Ramakrishna

We present a case report of a 37-year-old woman with multiple sclerosis (MS) who developed nephrotic-range proteinuria secondary to membrano proliferative glomerulonephritis (MPGN)-like disease with mesangial C3 deposition without evidence of immune-complex deposition in the context of long-term interferon-β (IFN-β) therapy. The complete remission of proteinuria following cessation of IFN-β, st...

2016
Blandine Tramunt Alexandre Buffet Solange Grunenwald Delphine Vezzosi Antoine Bennet Eric Huyghe Slimane Zerdoud Philippe Caron

In a patient with multiple endocrine neoplasia type 2A (MEN2A), an inverted physiological ratio between urinary normetanephrines and metanephrines is an early marker of recurrence in epinephrine-secreting pheochromocytoma, and 131I MIBG treatment appears to be a useful therapeutic option in order to avoid multiple invasive surgical procedures in pheochromocytomatosis.

2012
Ezzat Tarek Rajeev Paramesawaran Ben Phillips Greg Sadler

Patients with multiple endocrine neoplasia (MEN) type 2A develop medullary thyroid cancer, which is associated with poor prognosis in its metastatic stage. Hyperparathyroidism is a common finding in both MEN 1 and 2. We report a 68-year-old patient diagnosed clinically with MEN 1 based on the presence of hyperparathyroidism and pituitary Cushing's disease with no supporting genetic evidence. T...

Journal: :World Journal of Endocrine Surgery 2014

2012
Sam W. Moore Monique Zaahl

The risk of patients with Hirschsprung's disease later developing multiple endocrine neoplasia remains a matter of concern. The multiple endocrine neoplasia 2-Hirschsprung's disease association has been shown to cosegregate in Hirschsprung's disease patients with both short- and long-segment aganglionosis, although patients with long-segment aganglionosis a to carry the greatest risk. The Hirsc...

Journal: :Cancer research 1997
L V Debelenko M R Emmert-Buck P Manickam M Kester S C Guru E M DiFranco S E Olufemi S Agarwal I A Lubensky Z Zhuang A L Burns A M Spiegel L A Liotta F S Collins S J Marx S C Chandrasekharappa

Multiple endocrine neoplasia type 1 (MEN1) is an inherited syndrome characterized by development of multiple endocrine tumors in affected individuals. The gene responsible for the disease has been mapped to chromosome 11q13 by linkage analysis, but the gene itself has not yet been identified. We allelotyped 33 affected individuals from an extensive MEN1 kindred using eight polymorphic markers l...

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