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PITUITARY EXTRAMEDULLARY PLASMACYTOMA WITHOUT ANY SYSTEMIC INVOLVEMENT: A RARE CASE REPORT

RAFİYE ÇİFTCİLER, PINAR KARABAĞLI, MERT ŞAHİNOĞLU, HAKAN KARABAĞLI

Journal of Current Hematology & Oncology Research - 2025;3(1):15-17

Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Selçuk University, Konya, Turkiye

 

Extramedullary plasmacytoma (EMP) is a rare soft tissue plasma cell disorder without systemic involvement like multiple myeloma (MM). It develops outside of the bone marrow. It happens seldom for a plasma cell neoplasm to manifest as an intracranial or cranial tumor, and it is much less common for it to resemble a pituitary adenoma. In patients with sellar area plasmacytomas, headaches, cranial nerve deficits, visual abnormalities, bloody nasal discharge, and discomfort in the eyes and craniofacial regions are common presentations. A biopsy is required to make the diagnosis. For parasellar plasmacytomas to be successfully managed, an accurate diagnosis is essential. Overall, patient survival is excellent, although it might be lowered if they go on to develop overt MM. Suppose there is no known history of MM. In that case, it is advised to do a thorough workup to identify any underlying MM or to closely monitor any MM development in the future. In this study, we aimed to report a rare case who presented with loss of vision without systemic involvement of MM and whose pituitary biopsy was a plasmacytoma.