Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2021) 73 AEP399 | DOI: 10.1530/endoabs.73.AEP399

1Jagiellonian University Medical College, Department of Endocrinology, Kraków, Poland; 2M. Sklodowska-Curie Memorial Institute — Cancer Centre, Gliwice Branch, Department of Nuclear Medicine and Endocrine Oncology, Gliwice, Poland


Background

Multiple neuroendocrine neoplasia type 1 is a rare, heterogeneous genetic disorder with an autosomal dominant inheritance, predisposing to benign and malignant tumors. The phenotype of MEN1 syndrome varies between patients in terms of tumor localisation, age of onset and clinical aggressiveness, even between affected members of the same family. We report a heterogenic phenotype of the MEN1 variant c.[781C > T] (LRG_509t1) previously reported only once in a family with isolated hyperparathyroidism.

Methods

A large Polish kindred with suspicion of MEN1 syndrome underwent clinical evaluation and genetic testing.

Results

A heterozygous missense variant in exon 4 of the gene was identified in the sequence of the MEN1 gene (LRG_509t1), i.e. c.781C > T, leading at protein level to the amino acid change p.Leu261Phe in three-generation family. In the screened family, 5/6 affected members already developed hyperparathyroidism. In the index patient and two other family members, aggressive course of the disease, with dissemination of pancreatic-neuroendocrine tumor (insulinoma and non-functioning neuroendocrine tumors) was observed. In the index patient, late diagnosis and slow progression of the dissemination process was observed during 24 years of follow-up.

Conclusion

The very rare variant of MEN1, LRG_509t1 c.781C > T /p.Leu261Phe (LRG_509t1) diagnosed within a three -generation family has heterogenic clinical presentation. Further follow-up of the family members should be performed to confirm the spectrum and exact time of clinical presentation of this alteration.

Volume 73

European Congress of Endocrinology 2021

Online
22 May 2021 - 26 May 2021

European Society of Endocrinology 

Browse other volumes

Article tools

My recent searches

No recent searches.