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SM Journal of Sarcoma Research

Malignant Solitary Fibrous Tumor: Case Report

[ ISSN : 3068-0700 ]

Abstract
Details

Received: 28-Jun-2019

Accepted: 12-Aug-2019

Published: 14-Aug-2019

Case Report | Volume 3 - Issue 1 | Article DOI :

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Giselle Almeida¹* (ICAVC), Lucas Jacometo Coelho de Castilho¹ (ICAVC), Gisele Aparecida da Costa Gonçalves Pires¹ (ICAVC), Priscila Souza Schinzari² (UNISA) and Isabela Moraes Bernal² (UNISA)

¹Instituto do Câncer Dr Arnaldo Vieira de Carvalho
²Universidade de Santo Amaro

Corresponding Author:

Giselle Almeida, Cancer Institute Dr. Arnaldo Vieira de Carvalho, São Paulo, Brazil, Email: gisa.almeida@gmail.com

Keywords

Soft tissue sarcomas; Raretumors; Case Report

Abstract

Soft tissue sarcomas (Sts) are rare tumors that make up about 1% of malignant neoplasms. In addition to their histological diversity, Stscan occur anywhere on the body but present predominance in end areas. We aim to describe a case of soft tissue sarcoma because it is a rare malignant neoplasm. We report the case of a male patient, 60 years old, with a previous history of lung adenocarcinoma that started with diffuse abdominal pain with progressive worsening requiring surgical approach presenting histopathological findings compatible with malignant solitary fibrous tumor. He underwent adjuvant chemotherapy but evolved with disease progression. Another surgical approach was performed but due to the extension of the disease, complete resection was not possible and local IMRT radiotherapy was then chosen. The patient has been in clinical follow-up since 2015 considering that the disease has been presenting a slight reduction in its size in the imaging studies.

Citation

Almeida G, Castilho LJCD , Pires GADCG, Schinzari PS and Bernal IM. Malignant Solitary Fibrous Tumor: Case Report. SM J Sarcoma Res. 2019; 3(1): 1014.