Ali Syed Asad, Muhammad Agha Taj, Soomro Abdul Ghani, Siddiqui Akmal Jamal
Department of Surgery, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
J Ayub Med Coll Abbottabad. 2010 Jul-Sep;22(3):228-9.
The case of 20 years old boy with an extra osseous Ewing's sarcoma is described. He was initially diagnosed as a case of infiltrative malignant tumour of left suprarenal gland on the basis of preoperative workup but postoperative biopsy of surgically excised specimen confirmed Extra-osseous Ewing's Sarcoma (EES) suprarenal gland with no evidence of malignancy on skeletal scintiscan, bone marrow aspirate and histopathology Suprarenal location of primary EES is unknown and probably has not been reported in literature. We report a unique case of EES.
本文描述了一名20岁患有骨外尤文肉瘤的男孩的病例。根据术前检查，他最初被诊断为左肾上腺浸润性恶性肿瘤，但手术切除标本的术后活检证实为肾上腺骨外尤文肉瘤（EES），骨骼闪烁扫描、骨髓穿刺和组织病理学检查均未发现恶性证据。原发性EES的肾上腺定位尚不清楚，可能在文献中也未被报道。我们报告了一例独特的EES病例。
