Primary Angiosarcoma of spleen –A rare case report from rural hospital
Journal Title: Indian Journal of Pathology and Oncology - Year 2017, Vol 4, Issue 2
Abstract
Primary angiosarcoma of the spleen is a very rare malignant neoplasm. It comprises less than 1% of all splenic sarcomas. It may present with non-traumatic spontaneous rupture of the spleen and lethal hemorrhage. It is difficult to diagnose clinically and has a variable morphological spectrum. It is a highly aggressive malignant tumor having poor prognosis. It is usually found in adults above 40 years of age. A 22 year old female presented with abdominal pain and mass of four month duration. Physical examination revealed splenomegaly and diffuse tenderness all over the abdomen. Following computed tomography scan a possible clinical diagnosis of giant cavernous hamangioma of the spleen was made. Histopathology following splenectomy revealed angiosarcoma. We report this rare case along with review of literature.
Authors and Affiliations
Varsha Pandey, V. Sudarshan, Shiv Chandraker, K. S. Chandrakar
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