DOI: https://doi.org/10.5281/zenodo.17910451
VOLUME 2, DECEMBER ISSUE 10
Rania El Mouhib*, Walid Chair, Amine Maazouz, Imad El Azzaoui, Mahmoud Dabbagh, Mohammed Najih, Hakim El Kaoui, Sidi Mohamed Bouchentouf and Mountassir Moujahid
ABSTRACT
Adrenal cystic lymphangioma (ACL) is an exceptionally rare benign tumor resulting from a developmental malformation of lymphatic vessels within the adrenal gland. We report two cases managed in our department, highlighting the clinical, radiological, histopathological, and therapeutic features of this unusual entity. Diagnosis relies on imaging and is confirmed by histopathological examination. Complete surgical excision remains the treatment of choice, ensuring a favorable outcome and excellent prognosis.
Keywords:
Adrenal gland, cystic lymphangioma, benign tumor, imaging, adrenalectomy, retroperitoneum.