Goudarzipour Kourosh, Farahmandi Farzaneh, Mohammadi Ahmad, Taherian Reza
Student Research Committee, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Iran J Kidney Dis. 2018 May;12(3):190-192.
Ewing sarcoma/peripheral primitive neuroectodermal tumor (ES/PNET) typically occurs in long or flat bones, soft tissues, or less often, solid organs. Ewing sarcoma/peripheral primitive neuroectodermal tumor arising from the adrenal gland is extremely rare, especially in children, and only limited cases are reported previously. Herein, we review a case of a 22-month-old girl who presented to our department with abdominal pain, bulging of the left flank, and a nonfunctioning adrenal lesion which was found to be an adrenal ES/PNET. The patient was successfully treated with surgery and adjuvant chemotherapy. Since delayed diagnosis may result in metastatic lesions, this case underscores the importance of considering ES/PNET in the differential diagnosis of large adrenal masses.
尤因肉瘤/外周原始神经外胚层肿瘤(ES/PNET)通常发生于长骨或扁骨、软组织,较少发生于实体器官。起源于肾上腺的尤因肉瘤/外周原始神经外胚层肿瘤极为罕见,尤其是在儿童中,此前仅有有限的病例报道。在此,我们回顾了一例22个月大的女童,她因腹痛、左侧腰部膨隆就诊于我科,检查发现肾上腺有一个无功能病变,结果为肾上腺ES/PNET。该患者通过手术及辅助化疗成功治愈。由于延迟诊断可能导致转移性病变,该病例强调了在肾上腺大肿块的鉴别诊断中考虑ES/PNET的重要性。