Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe. (19th April 2013)

• Record Type: Journal Article
• Authors: Oriola, J; Biarnes, J; Hernandez, C; Simó, R
• Is Part Of: Clinical genetics. Volume 83:Number 4(2013:Apr.)
• Page Start: 384
• Page End: 387
• Publication Date: 2013-04-19
• Subjects: cancer -- endocrine -- MEN2 -- RET proto‐oncogene; Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/j.1399-0004.2012.01921.x
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract : Mutations in RET proto‐oncogene cause multiple endocrine neoplasia 2A (MEN2A). Mutations in codons 609 and 611 are not frequent. We identified two MEN2A families with the Cys609Phe RET mutation, which turned out to be the same family. This mutation has been described a couple of times with no clinical details. We have characterized the clinical phenotype of this large kindred. A 54‐year‐old woman, with a medullary thyroid carcinoma (MTC), and a 33‐year‐old woman, who was operated on for an adrenal pheochromocytoma, were the index cases. 35 relatives were studied. Sixteen turned out to be carriers and 12 of them have been operated on. This family showed eight patients with C‐cell hyperplasia, six patients affected by MTC and two showing pheochromocytoma. A papillary thyroid carcinoma was also found, together with the MTC, in one of the carriers. The phenotype in this large kindred is clearly of MEN2A. In carriers presenting the Cys609Phe mutation, the timing of the presentation of the syndrome is highly unpredictable. Therefore, a strict follow up of MTC must be carried out because of risk, and pheochromocytoma should not be ignored. These results reinforce the scarce data observed on this particular mutation.