Your browser doesn't support javascript.
loading
Primary and metastatic renal hemangiopericytoma.
Martín Martín, Sergio; Torrecilla Garcia-Ripoll, Juan Ramón; Trueba Arguiñarena, Francisco Javier; Cortiñas Gonzalez, Jose Ramon.
Afiliación
  • Martín Martín S; Urology Department. Hospital Clínico Universitario Valladolid. Spain.
Arch Esp Urol ; 67(8): 704-7, 2014 Oct.
Article en En, Es | MEDLINE | ID: mdl-25306989
ABSTRACT

OBJECTIVE:

Haemangiopericytoma is an uncommon perivascular tumor that occurs more frequently in soft tissues and is extremely rare in the kidney.

METHODS:

We report two cases The first one is the case of a 57-year-old man with bilateral metastatic renal haemangiopericytoma which appeared 18 years after removal of a meningeal haemangiopericytoma. The second is a 29-year-old woman with a primary kidney haemangiopericytoma that was casually found in a nephrectomy piece.

RESULTS:

In the first case, radical left nephrectomy and right renal mass radiofrequency ablation were performed. The patient had an uneventful postoperatory recovery. He remained disease-free 22 months after surgery but two new lesions appeared that were treated with radiofrequency ablation. The second case was a casual finding, a small tumor that had been totally resected.

CONCLUSIONS:

Haemangiopericytoma is a rare tumor with an uncertain clinical behaviour. Long-term follow up is important as local recurrences and metastases can develop years after initial treatment.
Asunto(s)
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hemangiopericitoma / Neoplasias Renales Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En / Es Revista: Arch Esp Urol Año: 2014 Tipo del documento: Article
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hemangiopericitoma / Neoplasias Renales Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En / Es Revista: Arch Esp Urol Año: 2014 Tipo del documento: Article