Nejati P, Amirian F, Sadeghi M, Karami K, Ramezani M. Solitary Fibrous Tumor of Testis: A rare Case with Review of Literature. Iranian Journal of Blood and Cancer 2020; 12 (1) :34-37
URL:
http://ijbc.ir/article-1-922-en.html
1- Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran
2- Molecular Pathology Research Center, Imam Reza hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran
3- Students Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran
4- Molecular Pathology Research Center, Imam Reza hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran , mazaher_ramezani@yahoo.com
Abstract: (3232 Views)
Solitary fibrous tumors (SFTs) more commonly arise in the pleura but recently, they have been reported in several extrapleural organs. Urogenital localization is rare, and only small numbers of cases of paratesticular SFT have been reported. An 81-year-old male with a history of colon carcinoma and complaint of testis swelling was referred for evaluation of a right paratesticular mass. Physical examination revealed a 2 cm oval-shaped paratesticular mass and herniation of intestinal loops in the right inguinal region after cough and Valsalva maneuver. An ultrasound examination was found in the upper pole of testis a well-defined hypoechoic mass in favor of testicular mass. It also revealed moderate to severe bilateral hydrocele and calcified wall in favor of benign lesion. In conclusion, SFT should be considered in the differential diagnosis of paratesticular masses and needs to be confirmed by IHC. CD34 and CD99 biomarkers are useful for confirmation of SFT.
:
Case report |
Subject:
Adults Hematology & Oncology Received: 2019/08/9 | Accepted: 2020/04/19 | Published: 2020/05/2