| Literature DB >> 2655361 |
L De Vriese1, M De Coster, D Noyez.
Abstract
Angiosarcomatous tumours of the spleen are rather rare. We report such a tumor in a 46 year old male. The pathology is described as well as a review of the literature. The pathogenesis is unknown, the symptomatology indistinct but spontaneous rupture is a rare event. Definite diagnosis is only possible with exploratory laparotomy and splenectomy. The prognosis is poor.Entities:
Mesh:
Year: 1989 PMID: 2655361
Source DB: PubMed Journal: Acta Chir Belg ISSN: 0001-5458 Impact factor: 1.090