Year: 2024
Type: article
Study design: Case Report
Abstract: INTRODUCTION/BACKGROUNDEctopic pituitary adenomas are extremely rare tumours which develop outside the sella turcica. The most common locations are the sphenoid sinus, clivus, suprasellar space, nasopharynx and cavernous sinus. Due to their rarity, these tumours are frequently misdiagnosed as other skull lesions such as chordoma, chondrosarcoma, meningioma or astrocytoma. We present a case of ectopic giant prolactinoma mimicking as clival chordoma. CASEA 38-year-old nulliparous female presented with oligomenorrhoea since the age of 20 and secondary amenorrhea at the age of 38 associated with galactorrhoea. Otherwise, she denied headache, symptoms of increased ICP or blurring of vision. There were no other symptoms to suggest pituitary hyper- or hypofunction. Her initial hormonal work-up showed hyperprolactinemia (>8000 ng/mL) with hypogonadotropic hypogonadism. MRI of the brain was signed out as clival chordoma measuring 2.3 x 3.6 x 4.1 cm displacing the pituitary gland and infundibulum. She underwent a biopsy of the lesion and the HPE confirmed pituitary lactotroph adenoma. She was started on cabergoline and her prolactin levels reduced significantly. CONCLUSIONEctopic pituitary adenomas occurring in the clivus are very rare. The main differential diagnosis to be considered is chordoma. Other than radiological imaging, additional endocrinological workup may be useful as well to establish the diagnosis. Biopsy of the lesion should be performed whenever the diagnosis is in doubt, as medical treatment with cabergoline often yields favourable outcomes in cases of ectopic prolactinoma which leads to a reduction in tumour size and prolactin level.
Authors: Kai Xuan Teh, Hwee Ching Tee, Jin Hui Ho
Institution: Hospital Tengku Ampuan Afzan
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W4411575720