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Multiple endocrine neoplasia type 2A [PDF]

Kaohsiung Journal of Medical Sciences, 2012
Multiple endocrine neoplasia type 2A (MEN 2A) is an autosomal dominant inherited cancer syndrome that expresses nonendocrine and endocrine tumors.
Chiung-Tang Huang, Wen-Chi Yang, Sheng-Fung Lin   +2 more
doaj   +6 more sources

Preimplantation Genetic Testing of Multiple Endocrine Neoplasia Type 2A [PDF]

Frontiers in Endocrinology, 2020
Background: When discussing matters of reproduction, the 2015 revised guidelines for the management of medullary thyroid carcinoma recommend that patients diagnosed with multiple endocrine neoplasia type 2A (MEN 2A) are informed about the option of ...
Anders Würgler Hansen, Anders Würgler Hansen, Laura Kirstine Sønderberg Roos, Kristine Løssl, Christian Godballe, Christian Godballe, Jes Sloth Mathiesen, Jes Sloth Mathiesen   +7 more
doaj   +5 more sources

A Case Study of Multiple Endocrine Neoplasia Type 2A. [PDF]

Cureus, 2022
Multiple endocrine neoplasia type 2 is an autosomal dominant neoplastic syndrome with subtypes multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, and familial medullary thyroid carcinoma. Medullary thyroid carcinoma universally coincides with multiple endocrine neoplasia type 2.
Yang CM.
europepmc   +3 more sources

Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A [PDF]

Frontiers in Endocrinology, 2021
To the best of our knowledge, we report a case of MEN2A complicated by moyamoya syndrome. A 52-year-old woman presented with vertigo. Magnetic resonance angiography (MRA) revealed bilateral supraclinoid stenosis of the internal carotid artery and ...
Fumihiro Matano, Yasuo Murai, Atsushi Watanabe, Kazutaka Shirokane, Takehito Igarashi, Kazuo Shimizu, Takashi Shimada, Akio Morita   +7 more
doaj   +2 more sources

Progressive metastatic pheochromocytoma induced by multiple endocrine neoplasia type 2A with a lethal outcome [PDF]

IJU Case Reports, 2022
Introduction Patients with multiple endocrine neoplasia type 2A (MEN2A) harboring a pathological variant in the RET gene are characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and hyperparathyroidism.
Koshiro Nishimoto, Noriaki Lukas Santo, Masato Yonamine, Kazuhiro Takekoshi, Go Kaneko, Suguru Shirotake, Hisayo Fukushima, Yoshitaka Okada, Masanori Yasuda, Akihiro Sakurai, Masafumi Oyama, Kento Kanao   +11 more
doaj   +2 more sources

Left anterior descending artery disease in a 27-year-old with multiple endocrine neoplasia, type 2A: A case report [PDF]

SAGE Open Medical Case Reports, 2023
Multiple endocrine neoplasia 2A is an autosomal dominant disease characterized by medullary thyroid cancer, pheochromocytoma, and primary hyperparathyroidism. Coronary artery disease is associated with the disorder, but the mechanism is unclear.
Mohammed Omar Al Salihi, Murali K Iyyani, Sarina Koilpillai, Gerson Quintero, Jorge Parellada, SJ Carlan   +5 more
doaj   +2 more sources

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study [PDF]

Endocrine Connections, 2020
Objective: Multiple endocrine neoplasia type 2A (MEN 2A) is a rare syndrome caused by RET germline mutations and has been associated with primary hyperparathyroidism (PHPT) in up to 30% of cases.
Louise Vølund Larsen, Delphine Mirebeau-Prunier, Tsuneo Imai, Cristina Alvarez-Escola, Kornelia Hasse-Lazar, Simona Censi, Luciana A Castroneves, Akihiro Sakurai, Minoru Kihara, Kiyomi Horiuchi, Véronique Dorine Barbu, Francoise Borson-Chazot, Anne-Paule Gimenez-Roqueplo, Pascal Pigny, Stephane Pinson, Nelson Wohllk, Charis Eng, Berna Imge Aydogan, Dhananjaya Saranath, Sarka Dvorakova, Frederic Castinetti, Attila Patocs, Damijan Bergant, Thera P Links, Mariola Peczkowska, Ana O Hoff, Caterina Mian, Trisha Dwight, Barbara Jarzab, Hartmut P H Neumann, Mercedes Robledo, Shinya Uchino, Anne Barlier, Christian Godballe, Jes Sloth Mathiesen   +34 more
doaj   +2 more sources

Phaeochromocytoma recurrence in a patient with multiple endocrine neoplasia type 2A. [PDF]

J Surg Case Rep, 2020
Abstract Multiple endocrine neoplasia type 2A (MEN2A) is a hereditary syndrome associated with tumours of the endocrine system. Principally, it is characterized by medullary thyroid carcinoma (MTC) with some individuals also developing phaeochromocytoma and hyperparathyroidism.
Gupta R.
europepmc   +5 more sources

[Metastatic pheochromocytoma in multiple endocrine neoplasia type 2A]. [PDF]

Probl Endokrinol (Mosk)
Pheochromocytoma (PHEO) currently is considered to be malignant due to metastatic potential. One of the most common familial forms of PHEO is multiple endocrine neoplasia syndrome (MEN) type 2. The penetrance of PHEO in MEN2 syndrome is up to 50% of cases. It may be one- or two-sided, but metastases occur extremely rare.
Rebrova DV, Rusakov VF, Krasnov LM, Fedorov EA, Chinchuk IK, Vorokhobina NV, Shikhmagomedov SS, Semenov AA, Chernikov RA, Sleptsov IV, Gavton GI, Imyanitov EN.   +11 more
europepmc   +3 more sources

Pheochromocytoma arising from an ectopic adrenal tissue in multiple endocrine neoplasia type 2A [PDF]

Endocrinology, Diabetes & Metabolism Case Reports, 2019
A 21-year-old woman was referred to our hospital to treat bilateral pheochromocytomas (PCCs) after a diagnosis of multiple endocrine neoplasia type 2A (MEN2A). We performed bilateral laparoscopic adrenalectomy.
Haruyuki Ohsugi, Nae Takizawa, Hidefumi Kinoshita, Tadashi Matsuda   +3 more
doaj   +2 more sources