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Background Steroid cell tumours of the ovary account for approximately 0.1% of all ovarian tumours. Association of these tumours with Von Hippel–Lindau syndrome is an extremely rare phenomenon. Case A 24-year-old female, diagnosed with Von Hippel–Lindau syndrome, with previous surgeries for cervical haemangioblastomas and pheochromocytoma was evaluated in the Reproductive Medicine Unit for secondary...
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