Context: The clinical phenotype of multiple endocrine neoplasia type 4 (MEN4) is undefined due to a limited number of published cases. Knowledge on disease manifestation in MEN4 is essential for developing prevention programs and treatment. Objective: To expand current knowledge of the MEN4 phenotype including assessment of penetrance. Design: This is a case report and a brief review of previously published MEN4 cases. Patients: We report a large Danish family with multiple cases of endocrine tumors that segregated with a pathogenic variant in the CDKN1B gene. Main Outcome/Result: The medical history of the proband included primary hyperparathyroidism and Cushing disease. Genetic analysis identified a pathogenic variant in CDKN1B (c.121-122delTT, p.Leu41Asnfs∗83). Among the family members, another 12 individuals were identified as carriers of the same variant, which segregated with development of endocrine tumors. Hypercalcemia due to primary hyperparathyroidism occurred in all 13 of the available carriers of the genetic variant, and 4 patients also had functioning or nonfunctioning pituitary adenomas, whereas 1 patient had a metastatic neuroendocrine tumor (carcinoid). Loss-of-heterozygosity was detected in two of five parathyroid adenomas, supporting that CDKN1B acts as a tumor suppressor gene. Thirty cases representing 16 different CDKN1B variants have previously been reported, and these cases presented primarily with primary hyperparathyroidism and functioning and nonfunctioning pituitary tumors. Conclusion: Hypercalcemia due to primary hyperparathyroidism and pituitary tumors are common in MEN4. Gastrointestinal neuroendocrine tumors appear to be less prevalent in MEN4 than in MEN1.
Bibliografisk noteFunding Information:
M.F. was supported by a grant from the Danish Independent Research Council. R.V.T. is funded by a Wellcome Trust Investigator Award, a National Institute for Health Research Senior Investigator Award, and the National Institute for Health Research Oxford Biomedical Research Centre Program.
Financial Support: M.F. was supported by a grant from the Danish Independent Research Council. R.V.T. is funded by a Wellcome Trust Investigator Award, a National Institute for Health Research Senior Investigator Award, and the National Institute for Health Research Oxford Biomedical Research Centre Program.
© 2019 Endocrine Society.