Indolfi Paolo, Donofrio Vittoria, Fusco Claudia, Di Martino Martina, Di Pinto Daniela, Indolfi Cristiana, Scanderbech Agostino Maioli Castriota, Casale Fiorina
Pediatric Department, Pediatric Oncology Service, Second University of Naples, Naples, Italy.
J Pediatr Hematol Oncol. 2010 Jul;32(5):e195-8. doi: 10.1097/MPH.0b013e3181e15c9e.
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive, vascular spindle-cell proliferation, with resemblance to Kaposi sarcoma. Usually, this tumor occurs in the skin and the retroperitoneum. We described a girl with a kidney localization and extension into the inferior vena cava and even into the right atrium. The case presented here is unique in 2 ways. First, kidney involvement of KHE has never been described in the literature until now. Second, and most remarkably, extensive tumor thrombosis suggests surgical excision even with cardiopulmonary bypass. The KHE of the kidney is a rare tumor but should be taken into account in the differential diagnosis with other pediatric renal neoplasms.
卡波西样血管内皮瘤(KHE)是一种罕见的、局部侵袭性的血管梭形细胞增殖性病变,与卡波西肉瘤相似。通常,这种肿瘤发生于皮肤和腹膜后。我们报道了一名女孩,肿瘤位于肾脏,并延伸至下腔静脉甚至右心房。此处报道的病例在两个方面具有独特性。首先,迄今为止,文献中从未描述过KHE累及肾脏的情况。其次,也是最显著的一点,广泛的肿瘤血栓形成提示即使需要体外循环也应进行手术切除。肾脏KHE是一种罕见肿瘤,但在与其他小儿肾肿瘤的鉴别诊断中应予以考虑。