Paratesticular leiomyosarcoma is very rare. We report a 72-year-old man with this scrotal tumor. The mass had been painless for eight years, but become painful and larger recently. A non-tender, firm, elastic mass was palpable on the right hemiscrotal wall, measuring 6 centimeters in diameter. The mass was not adhering to the testis or to the vas deferens. We performed a wide excision of the mass. The pathological diagnosis was compatible with a grade-2 leiomyosarcoma. The patient refused postoperative radiotherapy, of which the role remains controversial. He was doing well at nine months of follow-up. Local recurrence and/or distant metastasis have been reported for paratesticular leiomyosarcoma, though this rare tumor is often mistaken as...
Copyright © 2014 Ioannis Anastasiou et al. This is an open access article distributed under the Crea...
Herein we present 82-year-old man with leiomyosarcoma arising from the spermatic cord with scalp met...
We have read with great interest the article written by Ko and colleagues on a particularly rare typ...
Paratesticluar myxoid liposarcoma is rare, and it shares the similar clinical presentation with hydr...
Copyright © 2014 Shankar Haran et al.This is an open access article distributed under the Creative C...
We have read with great interest the article written by Ko et al. [1] on a particularly rare type of...
Paratesticular soft tissue sarcomas are very rare malignant mesenchymal tumors. With only few cases ...
Soft tissue sarcomas of the genitourinary tract are rare. Paratesticular sarcomas are extremely rare...
Paratesticular sarcomas are rare. Most cases reported in the literature are depending on retrospecti...
Paratesticularleiomyosarcomas are rare neoplasms. Radical orchidectomy and high ligation of cord fol...
Paratesticularleiomyosarcomas are rare neoplasms. Radical orchidectomy and high ligation of cord fol...
Soft-tissue sarcomas of the genitourinary tract account for only 1-2 % of urological malig-nancies a...
Paratesticular soft tissue tumours are remarkably rare entities, with malignant subtypes accounting ...
Sarcomas represent large and diverse group of malig-nant tumours, originating from mesenchymal cells...
Herein we present 82-year-old man with leiomyosarcoma arising from the spermatic cord with scalp met...
Copyright © 2014 Ioannis Anastasiou et al. This is an open access article distributed under the Crea...
Herein we present 82-year-old man with leiomyosarcoma arising from the spermatic cord with scalp met...
We have read with great interest the article written by Ko and colleagues on a particularly rare typ...
Paratesticluar myxoid liposarcoma is rare, and it shares the similar clinical presentation with hydr...
Copyright © 2014 Shankar Haran et al.This is an open access article distributed under the Creative C...
We have read with great interest the article written by Ko et al. [1] on a particularly rare type of...
Paratesticular soft tissue sarcomas are very rare malignant mesenchymal tumors. With only few cases ...
Soft tissue sarcomas of the genitourinary tract are rare. Paratesticular sarcomas are extremely rare...
Paratesticular sarcomas are rare. Most cases reported in the literature are depending on retrospecti...
Paratesticularleiomyosarcomas are rare neoplasms. Radical orchidectomy and high ligation of cord fol...
Paratesticularleiomyosarcomas are rare neoplasms. Radical orchidectomy and high ligation of cord fol...
Soft-tissue sarcomas of the genitourinary tract account for only 1-2 % of urological malig-nancies a...
Paratesticular soft tissue tumours are remarkably rare entities, with malignant subtypes accounting ...
Sarcomas represent large and diverse group of malig-nant tumours, originating from mesenchymal cells...
Herein we present 82-year-old man with leiomyosarcoma arising from the spermatic cord with scalp met...
Copyright © 2014 Ioannis Anastasiou et al. This is an open access article distributed under the Crea...
Herein we present 82-year-old man with leiomyosarcoma arising from the spermatic cord with scalp met...
We have read with great interest the article written by Ko and colleagues on a particularly rare typ...