Results 1 to 10 of about 8,627 (128)

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   +2 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

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   +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

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

Presentation of multiple endocrine neoplasia type 2A-associated ectopic cushing’s syndrome: case report and a systematic review [PDF]

Frontiers in Endocrinology
BackgroundMultiple endocrine neoplasia type 2 (MEN 2)-related ectopic Cushing’s syndrome (ECS) continues to present a clinical challenge due to its rarity and complexity.
Wei Wang, Wei-Ying Chen, Mei-Xian Zhang, Mei-Xian Zhang, Zhen-Yu Chen, Zhi-Lie Cao, Jun-Wei Wang, Wu-Gen Yao, Jian-Qiang Zhao, Fei-Ping Li, Hong-Yuan Yu, Jun Lu, Xiao-Ping Qi, Xiao-Ping Qi   +13 more
doaj   +2 more sources

Two sisters diagnosed with familial paraganglioma syndrome type 1 (FPGL1) and multiple endocrine neoplasia type 2A (MEN2A) [PDF]

World Journal of Surgical Oncology
Background In clinical practice, genetic testing has become standard for many cancerous diseases. While a diagnosis of a single hereditary syndrome is not uncommon, the coexistence of two genetic diseases, even with partially common symptoms, remains ...
Katarzyna Stawarz, Monika Durzynska, Adam Galazka, Monika Paszkowska, Karolina Bienkowska-Pluta, Jakub Zwolinski, Andrzej Tysarowski, Ewa Kwiatkowska, Agnieszka Podgorska   +8 more
doaj   +2 more sources

Efficacy of iodine-131-metaiodobenzylguanidine therapy for multiple endocrine neoplasia type 2A-associated metastatic pheochromocytoma: case report and literature review [PDF]

Endocrine Journal
Malignant transformation in multiple endocrine neoplasia type 2 (MEN2)-associated pheochromocytoma is rare, and there have been few reports of treatment with 131I-metaiodobenzylguanidine (MIBG) therapy.
Kentaro Suda, Noriko Kimura, Toshihiro Maeda, Shiro Watanabe, Sachiyo Nishida, Hiroaki Shima, Taro Sugawara, Shinya Uchino, Aki Ishikawa, Toshiaki Tanaka, Masato Furuhashi, Naoya Masumori, Akihiro Sakurai   +12 more
doaj   +2 more sources