Open Access
RESIDENT’S CORNER
Primary testicular leiomyosarcoma
Yakup Bostanci1, Ender Ozden2, Ekrem Akdeniz2,
Amir Kazzazi1, Bedri Kandemir2, Yarkin Kamil Yakupoglu2,
Bob Djavan1
1
Department of Urology, New York University School of Medicine, New York, New York, USA
2
Departments of Urology and Pathology, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey
Address correspondence to Dr. Yakup Bostanci, Department
of Urology, New York University School of Medicine, 150
East 32nd Street, New York, NY 10016 USA
Canadian Journal of Urology 2013, 20(2), 6730-6733.
Abstract
Primary testicular leiomyosarcoma is an extremely rare
tumor, and, to the best of our knowledge, only 20 cases in
adults have been reported in the literature to date. Herein,
we present a case of a 68-year-old man who complained
of left scrotal swelling for 2 months. Radiological
examination revealed a left testicular tumor with no
metastases to other organs. A left inguinal orchiectomy
was carried out and histopathologic examination revealed
an intratesticular leiomyosarcoma. The patient was treated
successfully by orchiectomy and received no adjuvant
therapy. During follow up until 12 months after surgery,
there has been no recurrence or metastases of the disease.
Keywords
leiomyosarcoma, sarcoma, testicular neoplasm
Cite This Article
APA Style
Bostanci, Y., Ozden, E., Akdeniz, E., Kazzazi, A., Kandemir, B. et al. (2013). Primary testicular leiomyosarcoma. Canadian Journal of Urology, 20(2), 6730–6733.
Vancouver Style
Bostanci Y, Ozden E, Akdeniz E, Kazzazi A, Kandemir B, Yakupoglu YK, et al. Primary testicular leiomyosarcoma. Can J Urology. 2013;20(2):6730–6733.
IEEE Style
Y. Bostanci et al., “Primary testicular leiomyosarcoma,” Can. J. Urology, vol. 20, no. 2, pp. 6730–6733, 2013.
Copyright © 2013 The Canadian Journal of Urology.