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The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A

Date

2010

Authors

Schulte, Klaus-Martin
Machens, Andreas
Fugazzola, Laura
McGregor, Alan
Diaz-Cano, Salvador J.
Izatt, Louise
Aylwin, Simon
Talat, N.
Beck-Peccoz, Paolo
Dralle, Henning

Journal Title

Journal ISSN

Volume Title

Publisher

Endocrine Society

Abstract

Background: Germline missense mutations of the RET protooncogene cause a clinical spectrum called multiple endocrine neoplasia (MEN) type 2. A strong genotype-phenotype correlation results in major implications for the clinical approach. More information on less common mutations is needed to advance specific guidance. Patients and Methods: We report individualized patient information on 36 carriers of the intracellular RET gene mutation S891A from three centers and clustered data of 38 former patients reported in the literature in nine additional studies. Results: S891A mutation accounts for up to 5% of all patients to date reported with RET mutations and 16% of those hitherto reported with intracellular mutations. S891A mutation caused medullary thyroid cancer (MTC) in 69.4%, pheochromocytoma in 2.8%, and parathyroid hyperplasia in 8.3% of the 36 patients of this case series and in 63.5, 4.1, and 4.1%, respectively, for the entire groups of 74 patients. The youngest age of onset for MTC in this group was 17 yr (median, 46 yr; range, 17-80 yr), for pheochromocytoma 46 yr (median, 46 yr), and for parathyroid hyperplasia 17 yr (median, 20 yr, range, 17-46 yr). Persistence of MTC was described in 14.3% of patients with available follow-up. Additional findings included corneal nerve thickening in three of 74 patients (4.1%). Conclusion: This intracellular mutation can initiate the full spectrum of MEN2a, initiates MTC at an early age, and causes recurrence and death if undertreated. We recommend stringent adherence to established guidance in MEN2a in this rare mutation.

Description

Keywords

protein Ret, alanine, protein Ret, RET protein, human, serine, cornea thickness, gene mutation, heterozygote, major clinical study, male, onset age, parathyroid hyperplasia

Citation

Source

Journal of Clinical Endocrinology and Metabolism

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.1210/jc.2010-0375

Restricted until

2099-12-31