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Srpski arhiv za celokupno lekarstvo 2018 Volume 146, Issue 3-4, Pages: 215-217
https://doi.org/10.2298/SARH170413135G
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Penile leiomyosarcoma

Grbić Dragan (Clinical Centre of Vojvodina, Department of Urology, Novi Sad)
Cantrell Alexander (University of California at Davis, Department of Urology, Sacramento, USA)
Šolajić Nenad ORCID iD icon (Institute of Oncology of Vojvodina, Department of Pathology, Sremska Kamenica + Medical Faculty, Novi Sad)
Dukić Mišo (Clinical Centre of Vojvodina, Department of Urology, Novi Sad)
Levakov Ivan (Clinical Centre of Vojvodina, Department of Urology, Novi Sad + Medical Faculty, Novi Sad)
Vojinov Saša (Clinical Centre of Vojvodina, Department of Urology, Novi Sad + Medical Faculty, Novi Sad)
Popov Mladen ORCID iD icon (Clinical Centre of Vojvodina, Department of Urology, Novi Sad + Medical Faculty, Novi Sad)
Levakov-Fejsa Aleksandra (Clinical Centre of Vojvodina, Center for Pathology and Histology, Novi Sad + Medical Faculty, Novi Sad)
Marušić Goran (Clinical Centre of Vojvodina, Department of Urology, Novi Sad + Medical Faculty, Novi Sad)

Introduction. Leiomyosarcoma of the penis (LSP) is an extremely rare form of penile tumor. LSP can be divided into two subtypes: deep and superficial. The goal of this manuscript is to present very rear case of LSP. Case outline. On exam, the patient presented with a slowly “growing penile bump“, for which an initial diagnosis of non-inflamed penile atheroma was given. Further diagnostic workup was omitted. Outpatient excisional biopsy was performed, and the tumor was sent for pathohistological examina-tion (PHE), which revealed LSP. The patient has not received any further treatment. The most recent follow up was 2.5 years after surgery, and the patient continues to do well without any complications. Conclusion. LSP is an extremely rare disease which can be cured if it is diagnosed in its early stage. PHE is necessary for diagnosis of LSP.

Keywords: penile tumor, penile atheroma, penile fibroma, penile leiomysarcoma