Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2012) 28 P275

SFEBES2012 Poster Presentations Pituitary (43 abstracts)

Aggressive prolactinoma treated with a large dose of dopamine agonist and radiotherapy

Sami Kenz & Peter Trainer


Endocrinology, Christie Hospital, Manchester, United Kingdom.


Introduction: Prolactinomas account for approximately 40% of all pituitary adenomas, with an estimated prevalence of 100 prolactinomas per million adults. Dopamine agonists currently represent the mainstay of treatment. Nevertheless, increasing dopamine-agonist dosage, surgery, and radiotherapy may be necessary in some cases, such as aggressive, dopamine-agonist resistant or atypical prolactinomas.

Case: We report the case of a 55 year old man who was incidentally found to have a large pituitary macroadenoma on MRI scan, during his investigations for persistent frontal headache. He was otherwise asymptomatic. MRI scan showed a large pituitary tumour 3.9×5.2 cm, extending from pituitary fossa filling the sphenoidal sinus, abutting the right carotid and encasing the left carotid artery and displacing the left temporal lobe. He was initially referred to the neurosurgeon and had a transsphenoidal biopsy, which confirmed the prolactinoma. He was then discussed at the MDT with the endocrinologists. His initial prolactin was >300,000 mU/L, T4 12,5 pmol/L TSH 2,98 mU/L Cortisol 248 nmol/l Testosterone 13,5 nmol/l. He was started on Cabergoline 0.5 mg per week, prolactin came down to 3000 mU/L with slight reduction in the size of the tumour. Unfortunately, despite perfect compliance his prolactin levels have risen and his tumour expanded. Prolactin levels rose to 21,000 mU/L, he has also complained of numbness in his face. His case re-discussed at the MDT, the consensus was little to be gained by debulking surgery. Cabergoline was gradually increased to 1.5 mg/day, and he completed 6 weeks cycle of radiotherapy. His symptoms have resolved completely with further reduction in the size of the tumour, his prolactin came down to 8000 mU/L.

Conclusion: Dopamine agonists are considered the gold standard of treatment in the majority of patients with prolactinomas. Only a small proportion of patients (10% in cabergoline-treated patients) do not respond successfully to dopamine agonists. Absence of prolactin control and of tumour shrinkage indicates resistance to dopamine agonists, which represents a challenging condition. Increasing dopamine agonist dosage and Radiotherapy are recommended as an alternative to surgery.

Declaration of interest: There is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.

Funding: No specific grant from any funding agency in the public, commercial or not-for-profit sector.

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