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原发性肾上皮样血管内皮瘤

Primary renal epithelioid hemangioendothelioma.

作者信息

Karasavvidou Foteini, Barbanis Sotirios, Gravas Stavros, Ioannou Maria, Oeconomou Athanasios, Pappa Dimitra, Melekos Michael D, Koukoulis George

机构信息

Department of Pathology, University Hospital, Larissa, Greece.

出版信息

Onkologie. 2009 Apr;32(4):203-5. doi: 10.1159/000203335. Epub 2009 Mar 19.

Abstract

BACKGROUND

Epithelioid hemangioendothelioma (EH) is a rare vascular neoplasm with an unpredictable malignant potential that has been described mainly in soft tissue, liver, and lung.

CASE REPORT

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.

CONCLUSIONS

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.

摘要

背景

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。

病例报告

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。

结论

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。

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