Results 21 to 30 of about 26,682 (180)

The Hirschsprung's-multiple endocrine neoplasia connection

Clinics, 2012
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 ...
Sam W. Moore, Monique Zaahl
doaj   +1 more source

Clinical case: multiple endocrine neoplasia type 1 (MEN 1)

Ожирение и метаболизм, 2012
Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands.

doaj   +1 more source

Bilateral pheochromocytoma with ganglioneuroma component associated with multiple neuroendocrine neoplasia type 2A: a case report

Journal of Medical Case Reports, 2017
Background Composite pheochromocytoma/paragangliomas are very rare tumors composed of ordinary pheochromocytoma paragangliomas associated with neurogenic tumors. Several hereditary susceptibility disorders are known to be associated with pheochromocytoma/
Boubacar Efared, Gabrielle Atsame-Ebang, Soufiane Tahirou, Khalid Mazaz, Nawal Hammas, Hinde El Fatemi, Laila Chbani   +6 more
doaj   +1 more source

Fast-growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1: a case report

Journal of Medical Case Reports, 2008
Introduction Predictive genetic screening and regular screening programs in patients with multiple endocrine neoplasia type 1 are intended to detect and treat malignant tumors at the earliest stage possible. Malignant neuroendocrine pancreatic tumors are
Waldmann Jens, Habbe Nils, Fendrich Volker, Slater Emily P, Kann Peter H, Rothmund Matthias, Langer Peter   +6 more
doaj   +1 more source

Multiple endocrine neoplasia type 2 – solving the puzzle

Journal of Family Medicine and Primary Care, 2023
Multiple endocrine neoplasia (MEN) are tumors that involve two or more endocrine glands. It can also involve other organs and tissues as well. Out of the four types of MEN type 2 is the most common.
Ajay K. Jha, Ashok Sunder, Sridhar Pradhan   +2 more
doaj   +1 more source

Primary hyperparathyroidism in multiple endocrine neoplasia type 1: when to perform surgery?

Clinics
Primary hyperparathyroidism is a common endocrinological disorder. In rare circumstances, it is associated with familial syndromes, such as multiple endocrine neoplasia type 1.
Francesca Giusti, Francesco Tonelli, Maria Luisa Brandi   +2 more
doaj   +1 more source

Multimodality appearance of multiple endocrine neoplasia type 1: A case report

Radiology Case Reports, 2019
Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells.
John Monge, MD, Daniel Homuth, DO, Loren Zuiderveld, MD   +2 more
doaj   +1 more source

Central Nervous System Tumors Among Infants in Canada: A Report From CYP‐C

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Central nervous system (CNS) tumors in infants are rare, pose unique clinical challenges, and lack large‐scale evidence‐based data to guide management. This study seeks to describe CNS tumors in Canadian infants and to compare their outcomes with those of older children.
Samuel Sassine, Hallie Coltin, Sylvia Cheng, Lucie Lafay‐Cousin, Vanan Issai Magimairajan, Craig Erker, Stéphanie Vairy, Lynette Bowes, Adam Fleming, Donna Johnston, Sarah McKillop, Roona Sinha, Julie Bennett, Christina Coleman, Laura Wheaton, Shayna Zelcer, Samuele Renzi, Thai Hoa Tran   +17 more
wiley   +1 more source

A Rare Combination: Multiple Endocrine Neoplasia Type 1 and Follicular Thyroid Carcinoma

Endocrinology Research and Practice, 2020
Multiple endocrine neoplasia Type 1 (MEN-1) is an inherited syndrome characterized by the development of endocrine tumors of the pancreas, parathyroid, and pituitary glands.
Ahmet GÖRGEL, Sacit Nuri GÖRGEL, Mustafa DEMİRPENÇE, Mitat BAHÇECİ   +3 more
doaj   +1 more source

Employment Trajectories of Patients With Systemic Lupus Erythematosus and Factors Driving Transitions Between States

Arthritis Care &Research, EarlyView.
Objective Systemic lupus erythematosus (SLE) significantly impacts employment capacity. This study aimed to investigate the impact of burden of disease activity, damage, and treatment on employment outcomes and transitions in patients with SLE. Methods Using data from a single center, we analyzed employment transitions, adjusted mean disease activity ...
Javier Mencia‐Ledo, Zahi Touma, Laura Whittall Garcia, Dafna D. Gladman, Behdin Nowrouzi‐Kia   +4 more
wiley   +1 more source