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ADRENOKORTİKAL ADENOMDA MYELOLİPOMATÖZ DEĞİŞİKLİKLER

CANAN FIRAT, SEDA ERYİĞİT, SERKAN YENER, TEVFİK DEMİR, OZAN BOZKURT, ÖMER DEMİR, BURÇİN TUNA, KUTSAL YÖRÜKOĞLU

Cukurova Medical Journal - 2019;44(3):1135-1138

Dr. Suat Seren Chest Diseases and Thorasic Surgery, Education and Research Hospital, Department of Pathology, İzmir, Turkey

 

Myelolipoma is a rare benign tumor which is generally detected incidentally. The tumor consists of mature fat tissue and hematopoietic cells that resemble bone marrow. The coexistence of myelolipoma and non-functional adrenocortical adenoma in the same gland is exceedingly rare. We herein present two cases of adrenal myelolipoma in association with non-functional adrenocortical adenoma in left adrenal gland of a 62-year-old woman and non-functional adrenocortical adenoma combined with myelolipoma and endothelial cyst, in right adrenal gland of a 73-years-old man. Microscopically, in the central of the tumor, there was a myelolipomatous area composed of adipocytes and hematopoietic cells surrounded by sheets of adenoma cells. The histopathological diagnosis was “myelolipomatous changes within a non-functional adrenocortical adenoma”. The cases are presented here with their rarity and pathological differential diagnosis.