Author(s)

Youness Chakir​^*, El Mahdi Graiouid, Jandou Issam, Mohamed Dakir, Adil Debbagh, Rachid Aboutaieb

Department of Urology, UHC Ibn Rochd, Casablanca, Morocco.

Adrenal myelolipoma is a benign, non-secreting tumor composed of adipose and myeloid tissue that can be complicated by retroperitoneal pain or hemorrhage. Its diagnosis is carried by the computed tomography (CT) and confirmed histologically. Surgery may be necessary in case of large volume, symptomatic mass or complication. We report the case of a 36-year-old patient who has a combination of myelolipoma and hereditary spherocytosis, which is extremely rare in the world literature. Computed tomography guided the diagnosis and surgical excision was performed because of the volume of the mass and its symptomatic nature. The evolution at two years was without recurrences.

Non-Secreting Tumor, Adipose Tissue, Myeloid Tissue, Adrenal Myelolipoma

Chakir​, Y. , Graiouid, E. , Issam, J. , Dakir, M. , Debbagh, A. and Aboutaieb, R. (2019) Adrenal Myelolipoma Associated with Spherocytosis: An Extremely Rare Case. Case Reports in Clinical Medicine, 8, 281-284. doi: 10.4236/crcm.2019.811034.