Endocrinology, Diabetes & Metabolism Case Reports (Sep 2020)

Identification of a TMEM127 variant in a patient with paraganglioma and acromegaly

  • Beryl Stütz,
  • Marta Korbonits,
  • Karl Kothbauer,
  • Werner Müller,
  • Stefan Fischli

DOI
https://doi.org/10.1530/EDM-20-0119
Journal volume & issue
Vol. 1, no. 1
pp. 1 – 5

Abstract

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The coincidence of a pheochromocytoma or paraganglioma and a pituitary adenoma in the same patient is a rare condition. In the last few years SDHx and MAX mutations have been identified and discussed as a potential causal connection in cases of coincidence. We describe a case of a middle-aged female patient which presented with acromegaly, a growth hormone-secreting pituitary adenoma and a symptomatic neck paraganglioma. The patient was cured by surgery from both the pituitary tumour and the paraganglioma and is well after ten years follow-up. Due to the unusual coexistence of two neuroendocrine tumours, further molecular genetic testing was performed which revealed a variant in the TMEM127 gene (c245-10C>G).

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