نتایج جستجو برای: multiple endocrine neoplasia

تعداد نتایج: 818926  

Journal: :Cancer control : journal of the Moffitt Cancer Center 2003
Melissa Alsina

Journal: :Neurology 2016
Aaron E Miller Daniel Pelletier

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...

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: :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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