Karasavvidou Foteini, Barbanis Sotirios, Gravas Stavros, Ioannou Maria, Oeconomou Athanasios, Pappa Dimitra, Melekos Michael D, Koukoulis George
Department of Pathology, University Hospital, Larissa, Greece.
Onkologie. 2009 Apr;32(4):203-5. doi: 10.1159/000203335. Epub 2009 Mar 19.
Epithelioid hemangioendothelioma (EH) is a rare vascular neoplasm with an unpredictable malignant potential that has been described mainly in soft tissue, liver, and lung.
We report a case of a primary renal EH in a 54-year-old woman who presented with a 3-month history of abdominal pain. Abdominal ultrasound and computed tomography scan revealed a solitary mass of 4.0 x 3.2 cm in the outer surface of the right kidney. Nephron-sparing surgery was performed. On the basis of the histological and immunohistochemical findings, the diagnosis of EH was made. The patient was free of disease 6 months after surgery.
Although EH may have a histologically benign appearance and can be treated using a nephron-sparing approach, this neoplasm is potentially malignant urging the need for a long-term follow-up in these patients.
上皮样血管内皮瘤(EH)是一种罕见的血管肿瘤,其恶性潜能不可预测,主要见于软组织、肝脏和肺。
我们报告一例54岁女性原发性肾EH,患者有3个月腹痛病史。腹部超声和计算机断层扫描显示右肾外表面有一个4.0×3.2 cm的孤立肿块。实施了保留肾单位手术。根据组织学和免疫组化结果,诊断为EH。患者术后6个月无疾病。
尽管EH在组织学上可能表现为良性,可采用保留肾单位的方法治疗,但这种肿瘤具有潜在恶性,因此需要对这些患者进行长期随访。