Endocrinology, Diabetes & Metabolism Case Reports (Jul 2019)

An unusual cause of gynaecomastia in a male

  • Tejhmal Rehman,
  • Ali Hameed,
  • Nigel Beharry,
  • J Du Parcq,
  • Gul Bano

DOI
https://doi.org/10.1530/EDM-19-0060
Journal volume & issue
Vol. 1, no. 1
pp. 1 – 4

Abstract

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Beta-human chorionic gonadotropin (βhCG) is normally produced by syncytiotrophoblasts of the placenta during pregnancy and aids embryo implantation. However, it is also secreted in varying amounts in non-pregnant conditions commonly heralding a neoplastic process. We present a case of 50-year-old man, who presented with bilateral gynaecomastia with elevated testosterone, oestradiol, suppressed gonadotropins with progressively increasing levels of human chorionic gonadotropin (hCG). Biochemical and radiological investigations including ultrasonography of testes, breast tissue, MRI pituitary and CT scan full body did not identify the source of hCG. FDG PET scan revealed a large mediastinal mass with lung metastasis. Immunostaining and histological analysis confirmed the diagnosis of primary choriocarcinoma of the mediastinum. It is highly aggressive and malignant tumor with poor prognosis. Early diagnosis and management are essential for the best outcome.