| Literature DB >> 31538490 |
Luigi Albano1, Marco Losa1, Giorgio Spatola2, Pietro Panni1, Maria Rosa Terreni3, Lina Raffaella Barzaghi1, Pietro Mortini1.
Abstract
Sellar melanocytomas represent a small subgroup of primary melanocytic tumors arising from leptomeningeal melanocytes. They are benign, slow-growing tumors with a high risk of recurrence. We report two cases of sellar melanocytoma treated at the same institute. A 35-year-old woman presented with amenorrhea and an intrasellar mass with suprasellar extension simulating a hemorrhagic pituitary adenoma. The second case is a 51-year-old man with progressive visual loss and a recurrence of primary sellar and suprasellar melanocytoma. The first patient underwent gross total resection and the second patient underwent subtotal resection. Neither of them was treated with postoperative adjuvant therapies. The second patient had tumor regrowth 75 months after surgery; he therefore underwent gamma knife radiosurgery. Both patients are alive and well at the last follow-up (140 and 93 months, respectively).Entities:
Keywords: Sellar melanocytoma; leptomeningeal melanocytes; pituitary tumor; primary melanocytic brain tumors; transsphenoidal surgery
Year: 2019 PMID: 31538490 DOI: 10.1080/02688697.2019.1667485
Source DB: PubMed Journal: Br J Neurosurg ISSN: 0268-8697 Impact factor: 1.596