Results 11 to 20 of about 1,690 (123)
Preoperative Metyrosine Administration for Bilateral Pheochromocytomas Following Pheochromocytoma Crisis: A Case Report. [PDF]
IJU Case RepABSTRACT Introduction Pheochromocytoma crisis complicated by catecholamine‐induced cardiomyopathy is a life‐threatening condition requiring careful preoperative management. Although metyrosine has recently been approved in Japan for the perioperative management of pheochromocytoma, clinical experience remains limited.
Demizu N +9 more
europepmc +2 more sources
Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A
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 +7 more
doaj +1 more source
Robot-Assisted Laparoscopic Partial Adrenalectomy Utilizing Intraoperative Indocyanine Green Near-Infrared Fluorescence Imaging for Pheochromocytoma: A Case Report. [PDF]
IJU Case RepABSTRACT Introduction Indocyanine green (ICG) near‐infrared fluorescence (NIRF) imaging facilitates pheochromocytoma identification during adrenal surgery. Case Presentation We report a 21‐year‐old woman with multiple endocrine neoplasia type 2A and bilateral adrenal tumors who underwent ICG‐NIRF–guided, robot‐assisted partial adrenalectomy for ...
Takizawa N +5 more
europepmc +2 more sources
Endocrine Connections, 2021 Risk of metastatic disease in the cluster 2-related pheochromocytoma/paraganglioma (PPGL) is low. In MEN2 patients, identification of origin of met astases from pheochromocytoma (PCC) or medullary thyroid carcinoma (MTC) is challenging as both are of ...
Sandeep Kumar +10 more
doaj +1 more source
Non-invasive prenatal diagnosis of multiple endocrine neoplasia type 2A using COLD-PCR combined with HRM genotyping analysis from maternal serum. [PDF]
PLoS ONE, 2012 The multiple endocrine neoplasia type 2A (MEN2A) is a monogenic disorder characterized by an autosomal dominant pattern of inheritance which is characterized by high risk of medullary thyroid carcinoma in all mutation carriers.
Hada C Macher +7 more
doaj +1 more source
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 +11 more
doaj +1 more source
The role of prophylactic parathyroidectomy during thyroidectomy for MTC in patients with MEN2A syndrome [PDF]
Folia Medica, 2023 Aim: To define the role of prophylactic parathyroidectomy in the surgical treatment of medullary thyroid carcinoma (MTC) in multiple endocrine neoplasia type IIa (MEN2A) syndrome through a literature review.
Christos Kavazis +5 more
doaj +3 more sources
Life, 2023 Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant (AD) condition with very high penetrance and expressivity. It is characterized into three clinical entities recognized as MEN2A, MEN2B, and familial medullary thyroid carcinoma (FMTC ...
Vassos Neocleous +4 more
doaj +1 more source
P023-CYS618SER MUTASYONLU BİR MEN2A AİLESİ
Endocrinology Research and Practice, 2022 -
Ekrem Algün +5 more
doaj +6 more sources
BMC Cancer, 2021 Background Germline RET mutations and variants are involved in development of multiple endocrine neoplasia type 2 (MEN2). The present study investigated a spectrum of RET variants, analyzed genotype-phenotype relationships, and evaluated their effect on ...
Xiao-Ping Qi +9 more
doaj +1 more source