Dev Retroperitoneal Hemanjioperisitoma: Vaka Sunumu

Hemangioperisitoma, kapiller perisitlerden köken alan, genellikle agresif seyreden, nüks-metastaz yapmaya meyilli ve nadir görülen bir yumuşak doku tümörüdür. Tümörün 5cm’den büyük olması, artmış mitotik aktivite, yüksek sellülarite, immatür veya pleomorfik tümör hücreleri, kanama ve nekroz odaklarının gözlenmesi malignitenin göstergeleridir. Temel tedavisi radikal cerrahidir. Bu olguda dev retroperitoneal hemanjioperisitoma nedeniyle opere edilen 48 yaşındaki erkek hastayı sunmayı amaçladık

Dev Retroperitoneal Hemanjioperisitoma: Vaka Sunumu

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