Al Haddabi Ibrahim, Al Bahri Maiya, Burney Ikram
Department of Pathology, College of Medicine, Sultan Qaboos University, Sultanate of Oman.
Indian J Pathol Microbiol. 2012 Oct-Dec;55(4):569-71. doi: 10.4103/0377-4929.107826.
Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) of the prostate is extremely rare. Here, we report a case of ES/PNET of prostate in a 24-year-old man presenting with dysuria and pelvic discomfort. Computed tomography scan revealed a heterogeneous mass involving the prostate without evidence of distant metastases. Histologically, the tumor was composed of small round blue cells strongly and diffusely positive for CD99 and epithelial markers. Fluorescence in situ hybridization confirmed rearrangement of the Ewing's sarcoma region on chromosome 22.
前列腺尤因肉瘤/原始神经外胚层肿瘤(ES/PNET)极为罕见。在此,我们报告一例24岁男性前列腺ES/PNET病例,该患者表现为排尿困难和盆腔不适。计算机断层扫描显示前列腺有一个不均匀肿块,无远处转移迹象。组织学上,肿瘤由小圆形蓝色细胞组成,CD99和上皮标记物呈强弥漫性阳性。荧光原位杂交证实22号染色体上尤因肉瘤区域发生重排。