[Liposarcoma of spermatic cord. A rare urologic tumor]
- PMID: 1444619
[Liposarcoma of spermatic cord. A rare urologic tumor]
Abstract
Malignant paratesticular tumors are uncommon. Of these, liposarcoma of the spermatic cord constitutes a rare tumor type with a good prognosis. It has a high rate of survival over 5 years. Inguinal orchiectomy generally suffices, although patients should be followed closely since local recurrence is not uncommon. The present study briefly reviews the literature on spermatic cord liposarcoma and reports an additional case that was treated exclusively by radical orchiectomy. Four years postoperatively the patient continues to be tumor-free.
Similar articles
-
[Liposarcoma of the spermatic cord: a report of a new case and a review of the literature].Actas Urol Esp. 1999 May;23(5):447-54. Actas Urol Esp. 1999. PMID: 10427822 Review. Spanish.
-
Liposarcoma of the spermatic cord: report of 6 cases and review of the literature.J Urol. 1995 Jan;153(1):154-7. doi: 10.1097/00005392-199501000-00055. J Urol. 1995. PMID: 7966755 Review.
-
[Liposarcoma of the spermatic cord in the left scrotum and inguinal region: a case report].Hinyokika Kiyo. 2000 May;46(5):349-51. Hinyokika Kiyo. 2000. PMID: 10876762 Japanese.
-
[Paratesticular tumor. Liposarcoma of the spermatic cord].Actas Urol Esp. 1993 Jun;17(6):392-6. Actas Urol Esp. 1993. PMID: 8368109 Review. Spanish.
-
[Liposarcoma of the spermatic cord. Review of the literature. Apropos of a case of myxoid liposarcoma].J Urol (Paris). 1989;95(2):107-10. J Urol (Paris). 1989. PMID: 2659676 Review. French.
Cited by
-
Myxoid liposarcoma of the spermatic cord: a case report and review of the literature.Int Urol Nephrol. 2003;35(3):369-72. doi: 10.1023/b:urol.0000022908.59378.8d. Int Urol Nephrol. 2003. PMID: 15160541 Review.