Boo Yoon-Jung, Fisher Jason C, Haley Mary Jo, Cowles Robert A, Kandel Jessica J, Yamashiro Darrell J
Division of Pediatric Surgery, Department of Surgery, Korea University College of Medicine, Seoul 136-705, Korea.
J Pediatr Surg. 2009 Oct;44(10):2031-6. doi: 10.1016/j.jpedsurg.2009.06.023.
Clear cell sarcoma of the kidney (CCSK) is uncommon pediatric renal tumor and can present a significant therapeutic challenge in those patients whose tumors spread beyond the kidney. Thus, identifying potential novel targets for treatment may be clinically important. Clear cell sarcoma of the kidney is characterized by a unique vascular pattern, in which nests of tumor cells are separated by regularly-spaced, fine fibrovascular septa. This distinctive histopathology raises the possibility that understanding the factors which drive angiogenesis in CCSK tumors may suggest new therapeutic targets. Here, we describe a case of CCSK and present immunohistochemical studies of its vasculature.
肾透明细胞肉瘤(CCSK)是一种罕见的儿科肾脏肿瘤,对于那些肿瘤已扩散至肾脏以外的患者而言,它可能构成重大的治疗挑战。因此,识别潜在的新型治疗靶点可能具有重要的临床意义。肾透明细胞肉瘤的特征是具有独特的血管模式,其中肿瘤细胞巢被规则间隔的细纤维血管间隔分隔开。这种独特的组织病理学特征增加了一种可能性,即了解驱动CCSK肿瘤血管生成的因素可能会提示新的治疗靶点。在此,我们描述了一例CCSK病例,并展示了对其脉管系统的免疫组织化学研究。