Results 1 to 10 of about 26,682 (180)

Multiple endocrine neoplasia 2: an overview

Therapeutic Advances in Chronic Disease, 2022
This review article discusses the diagnosis and treatment of patients with multiple endocrine neoplasia type 2 (MEN2). The most common tumors associated with MEN2 are those of the parathyroid, thyroid, and adrenal glands.
B Saravana-Bawan, JD Pasternak
doaj   +2 more sources

Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2

Clinics, 2012
Multiple endocrine neoplasia type 2 is an inherited cancer syndrome characterized by tumors of thyroid and adrenal tissues. Germline mutations of the REarranged during Transfection (RET) proto-oncogene, leading to its unregulated activation, are the ...
Simona M. Wagner, ShuJun Zhu, Adrian C. Nicolescu, Lois M. Mulligan   +3 more
doaj   +3 more sources

Multiple endocrine neoplasia syndrome

Український радіологічний та онкологічний журнал, 2021
Background. Multiple endocrine neoplasia type 1 is a rare inherited disease that combines heterogeneous autosomal inherited disorders, the pathogenesis of which is based on hyperplasia or tumor transformation of several neuro- endocrine glands.
М. В. Красносельський, А. В. Свинаренко, Н. С. Підченко, А. С. Сімбірьова   +3 more
doaj   +1 more source

Lady Surrounded by Multiple Endocrine Neoplasia (MEN) [PDF]

Bengal Physician Journal, 2023
Secondary adrenal insufficiency (SAI) had been diagnosed in a nondiabetic lady with recurrent hypoglycemia having low morning cortisol and low-normal adrenocorticotropic hormone.
Partha Pratim Chakraborty, Spandan Saha, Sriparna Das, Saumik Datta   +3 more
doaj   +1 more source

Pituitary tumors in patients with MEN1 syndrome

Clinics, 2012
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 ...
Luis V. Syro, Bernd W. Scheithauer, Kalman Kovacs, Rodrigo A. Toledo, Francisco J. Londoño, Leon D. Ortiz, Fabio Rotondo, Eva Horvath, Humberto Uribe   +8 more
doaj   +1 more source

Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1

Clinics, 2012
Primary hyperparathyroidism associated with multiple endocrine neoplasia type I (hyperparathyroidism/multiple endocrine neoplasia type 1) differs in many aspects from sporadic hyperparathyroidism, which is the most frequently occurring form of ...
Delmar M. Lourenço Jr., Flavia L. Coutinho, Rodrigo A. Toledo, Tatiana Denck Gonçalves, Fabio L. M. Montenegro, Sergio P. A. Toledo   +5 more
doaj   +1 more source

Variable clinical expression in patients with a germline MEN1 disease gene mutation: clues to a genotype-phenotype correlation

Clinics, 2012
Multiple endocrine neoplasia type 1 is an inherited endocrine tumor syndrome, predominantly characterized by tumors of the parathyroid glands, gastroenteropancreatic tumors, pituitary adenomas, adrenal adenomas, and neuroendocrine tumors of the thymus ...
Cornelis J. Lips, Koen M. Dreijerink, Jo W. Höppener   +2 more
doaj   +1 more source

Multiple Endocrine Neoplasia or Accidental Association?

European Journal of Case Reports in Internal Medicine, 2020
Pheochromocytoma, papillary thyroid carcinoma and hyperparathyroidism have rarely been reported together. Whether this association is coincidental or results from an unknown genetic predisposition is difficult to ascertain.
Georgiana Cristina Taujan, Felicia Baleanu, Linda Spinato, Ruth Duttmann, Rafik Karmali, Laura Iconaru   +5 more
doaj   +1 more source

Multiple endocrine neoplasia type 1

Orphanet Journal of Rare Diseases, 2006
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very high penetrance and an equal sex ...
Luzi Ettore, Gozzini Alessia, Sala Silvia, Monte Francesca, Falchetti Alberto, Marini Francesca, Brandi Maria   +6 more
doaj   +1 more source

Thymic atypical carcinoid tumors with elevated mitotic counts in a patient with multiple endocrine neoplasia: A case report

Thoracic Cancer, 2023
Thymic neuroendocrine tumors associated with multiple endocrine neoplasia are only defined as carcinoid and are not associated with large‐cell neuroendocrine carcinoma (LCNEC).
Shuntaro Hiro, Shuhei Teranishi, Tomoe Sawazumi, Satoshi Nagaoka, Chihiro Sugimoto, Hirokazu Nagayama, Wataru Segawa, Yukihito Kajita, Chihiro Maeda, Sousuke Kubo, Kenichi Seki, Ken Tashiro, Nobuaki Kobayashi, Masaki Yamamoto, Makoto Kudo, Takeshi Kaneko   +15 more
doaj   +1 more source