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Endocrine Abstracts (2023) 94 P126 | DOI: 10.1530/endoabs.94.P126

SFEBES2023 Poster Presentations RET (5 abstracts)

Characterising the natural history of Multiple Endocrine Neoplasia 2B caused by M918T RET pathogenic variants in children and young people

Sinead McGlacken-Byrne 1 , Colin Butler 2 , Tarek Abdel Aziz 2 , Louise Izatt 3 , Caroline Brain 1 & Tom Kurzawinski 2


1Department of Paediatric Endocrinology, Great Ormond Street Hospital, London, United Kingdom. 2Department of Endocrine Surgery, University College London Hospitals NHS Foundation Trust, London, United Kingdom. 3South East Thames Regional Genetics Service, Guy’s and St Thomas’ NHS Foundation Trust, London, United Kingdom


Aim: We describe the natural history, treatment, and clinical outcomes of Multiple Endocrine Neoplasia type 2B (MEN2B) caused by the M918T RET pathogenic variant.

Methods: Retrospective case notes review of all young people <18 years presenting to a quaternary paediatric endocrinology referral centre in the UK between 2005-2023 who have MEN2B caused by the M918T pathogenic variant in the RET proto-oncogene.

Results: Twelve children (7F, 58.3%, median age at genetic diagnosis 3.5yrs, range 0.1-16) with a confirmed heterozygous c.2753T>C M918T RET pathogenic variant (de novo in 66.7% (n=8), maternally inherited in 25% (n=3), and of unknown inheritance in 8.3% (n=1)) were included. Eleven (91.7%) had gastrointestinal manifestations: constipation (83.3%, n=10), intestinal ganglioneuromatosis (50%, n=6), and gallstones (25%, n=3). Mucosal neuromas were found in 58.3% (n=7) and alacrima in 25% (n=3). Three children (25%) had clinically palpable disease. All had thyroidectomy with central lymphadenectomy (median age 4.5yrs, range 0.3-16); two had lateral neck dissections. Preoperative calcitonin was 85ng/l (range 23-7120) with an undetectable calcitonin achieved postoperatively in 33.3% (n=4). Medullary thyroid cancer was confirmed on histopathology in 91.7% (n=11); one child had c-cell hyperplasia. Four children (33.3%) had nodal involvement. One child had metastasis to surrounding mediastinal structures and received adjuvant EBRT. Three children had later biochemical and/or clinical recurrence requiring reoperation (n=1) and/or selpercatinib or vandetinib treatment (n=3, treated for a range of 1-3 years). No child developed a phaeochromocytoma during the study surveillance period. One child died of a respiratory arrest unrelated to thyroid pathology.

Conclusions: Early diagnosis and thyroidectomy are essential for children with M918T-associated MEN2B. Gastrointestinal manifestations are characteristic and should raise diagnostic suspicion of this rare disease. Selective RET tyrosine kinase inhibitors show therapeutic efficacy in progressive disease.

Volume 94

Society for Endocrinology BES 2023

Glasgow, UK
13 Nov 2023 - 15 Nov 2023

Society for Endocrinology 

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