Results 61 to 70 of about 8,627 (128)

A germline RET proto-oncogene mutation in multiple members of an Arab family with variable onset of MEN type 2A-associated clinical manifestations

open access: yesEgyptian Journal of Medical Human Genetics, 2017
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

open access: yesTurkish Journal of Anaesthesiology and Reanimation
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

open access: yesClinics, 2012
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

Vaginal delivery in a patient with pheochromocytoma, medullary thyroid cancer, and primary hyperparathyroidism (multiple endocrine neoplasia type 2A, Sipple′s syndrome)

open access: yesSaudi Journal of Anaesthesia, 2014
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

open access: yesMolecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.
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

Robot‐Assisted Laparoscopic Partial Adrenalectomy Utilizing Intraoperative Indocyanine Green Near‐Infrared Fluorescence Imaging for Pheochromocytoma: A Case Report

open access: yesIJU Case Reports
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

Coexistence of Medullary Thyroid Carcinoma and Bilateral Pheochromocytoma in MEN2A Syndrome: Atypical Presentation and Clinical Insights From a Case Report

open access: yesClinical Case Reports
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]

open access: yesCancers (Basel), 2023
Holm M   +16 more
europepmc   +1 more source

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