Results 61 to 70 of about 8,627 (128)
Background: Multiple endocrine neoplasia type 2A (MEN2A) is a rare cancer associated-syndrome, inherited in an autosomal dominant fashion and caused by germline mutation in RET proto-oncogene.
Makia Marafie +4 more
doaj +1 more source
Challenging Perioperative Management of a MEN2A Syndrome Patient Complicated by Eisenmenger Syndrome
Multiple endocrine neoplasia type 2A (MEN2A), is associated with pheochromocytoma and medullary carcinoma of the thyroid. A surgical procedure in these patients can be complicated if they have any congenital heart disease (CHD).
Amit Rastogi +4 more
doaj +1 more source
RET codon 609 mutations: a contribution for better clinical managing
Medullary thyroid carcinoma currently accounts for 5-8% of all thyroid cancers. The clinical course of this disease varies from extremely indolent tumors that can go unchanged for years to an extremely aggressive variant that is associated with a high ...
Caterina Mian +4 more
doaj +1 more source
Multiple endocrine neoplasia 2A (MEN 2A), or Sipple′s syndrome is a rare inherited dominant syndrome, characterised by medullary thyroid carcinoma, adrenal pheochromocytoma and hyperparathyroidism, due to specific RET proto-oncogene mutations.
Muhammad Anas Muzannara +5 more
doaj +1 more source
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley +1 more source
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 ...
Nae Takizawa +5 more
doaj +1 more source
A Case Study of Multiple Endocrine Neoplasia Type 2A. [PDF]
Yang CM.
europepmc +1 more source
MEN2A may present with bilateral pheochromocytoma a decade before medullary thyroid carcinoma. This case highlights that high‐risk RET mutations must dictate surgical management regardless of benign cytology.
Juan Carlos Vallejo‐Soto +5 more
doaj +1 more source
Primary Hyperparathyroidism in Multiple Endocrine Neoplasia Type 2A in Denmark 1930–2021: A Nationwide Population-Based Retrospective Study [PDF]
Holm M +16 more
europepmc +1 more source
Anesthesia and Outcome of 33 Surgeries in 24 Multiple Endocrine Neoplasia Type 2A (MEN2A) Patients: A National Rare Disease Center's Experience. [PDF]
Li Y, Jin D, Shen L, Huang Y.
europepmc +1 more source

