Department of Urology, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
J Pediatr Surg. 2011 Sep;46(9):1849-51. doi: 10.1016/j.jpedsurg.2011.06.034.
Primary renal synovial sarcoma is a rare entity with fewer than 40 cases reported in the literature. Its clinical presentation and radiographic features, namely, its often complex cystic appearance, make it difficult to differentiate from other benign or malignant renal lesions. Although there are certain consistent morphological and immunohistochemical features, diagnosis ultimately depends on molecular studies. Prognosis is poor, and there currently exists no defined treatment protocol. Herein, we describe the youngest reported case of primary renal synovial sarcoma in the literature.
原发性肾脏滑膜肉瘤是一种罕见的实体瘤,文献中报道的病例不足 40 例。其临床表现和影像学特征,即其常呈现复杂的囊性外观,使其难以与其他良性或恶性肾脏病变区分。尽管存在某些一致的形态学和免疫组织化学特征,但最终诊断仍依赖于分子研究。预后较差,目前尚无明确的治疗方案。本文描述了文献中报道的年龄最小的原发性肾脏滑膜肉瘤病例。