Gland surgery · 2025
RET Y791F in MEN2: a variant presumed non-pathogenic, yet lacking conclusive evidence of insignificance.
СтатьяНазвание и аннотация: Перевод в очереди
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Binter Teresa, Niederle Martin Bruno, Arikan Melisa, Hargitai Lindsay, Schernthaner-Reiter Marie Helene, Baumgartner-Parzer Sabina, Niederle Bruno, Scheuba Christian, Riss Philipp
Аннотация
BACKGROUND: Patients with rearranged-during-transfection (RET) mutations may develop aggressive medullary thyroid carcinoma (MTC), pheochromocytoma (PCC) and primary hyperparathyroidism (PHPT) within the multiple endocrine neoplasia 2 (MEN2) syndrome, depending on the specific genotype. The Y791F variant has been subject to studies over time but opinions on how to deal with it differ. Pathogenicity could never be proven, nor entirely ruled out. This study aims to contribute to the assessment of its importance and necessity for clinical surveillance.
METHODS: Thirty-six patients with a pathogenic variant in codon Y791F were analysed in this retrospective clinical and biochemical follow-up study in terms of their clinical manifestation. The patients were diagnosed within a prospective calcitonin screening program of individuals with thyroid nodules, PCC and/or PHPT.
RESULTS: MTC was diagnosed in three index cases of patients aged between 56 and 69 years. Beside thyroid nodules, neoplastic C-cell hyperplasia (nCCH) was diagnosed in five index cases, aged between 48 and 69 years. One index patient presented with unilateral PCC at the age of 68 years and another with PHPT at the age of 54 years. The patients were longitudinally monitored for a median [min-max] of 101.5 [0-263] months from the time of mutation diagnosis to the last follow-up, thereby encompassing observation until reaching a median [min-max] age of 56.5 [18-82] years, assuming a lifelong condition.
CONCLUSIONS: Despite perceptions of clinical insignificance, ongoing uncertainties regarding potential clinical manifestations of MEN2 continue to surround the Y791F variant. There is an ambiguity between sporadic cases and MEN2 associated manifestations leaving the role of regular monitoring open for consideration.
METHODS: Thirty-six patients with a pathogenic variant in codon Y791F were analysed in this retrospective clinical and biochemical follow-up study in terms of their clinical manifestation. The patients were diagnosed within a prospective calcitonin screening program of individuals with thyroid nodules, PCC and/or PHPT.
RESULTS: MTC was diagnosed in three index cases of patients aged between 56 and 69 years. Beside thyroid nodules, neoplastic C-cell hyperplasia (nCCH) was diagnosed in five index cases, aged between 48 and 69 years. One index patient presented with unilateral PCC at the age of 68 years and another with PHPT at the age of 54 years. The patients were longitudinally monitored for a median [min-max] of 101.5 [0-263] months from the time of mutation diagnosis to the last follow-up, thereby encompassing observation until reaching a median [min-max] age of 56.5 [18-82] years, assuming a lifelong condition.
CONCLUSIONS: Despite perceptions of clinical insignificance, ongoing uncertainties regarding potential clinical manifestations of MEN2 continue to surround the Y791F variant. There is an ambiguity between sporadic cases and MEN2 associated manifestations leaving the role of regular monitoring open for consideration.