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Kaposiform Hemangioendothelioma of the Kidney: An Unusual Presentation of a Rare Vascular Neoplasm

Authors :
Claudia Fusco
Cristiana Indolfi
Paolo Indolfi
Agostino Maioli Castriota Scanderbech
Fiorina Casale
Daniela Di Pinto
Vittoria Donofrio
Martina Di Martino
Source :
Journal of Pediatric Hematology/Oncology. 32:e195-e198
Publication Year :
2010
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2010.

Abstract

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.

Details

ISSN :
10774114
Volume :
32
Database :
OpenAIRE
Journal :
Journal of Pediatric Hematology/Oncology
Accession number :
edsair.doi.dedup.....657878c63122b0cc0c2e051cf8799de1
Full Text :
https://doi.org/10.1097/mph.0b013e3181e15c9e