Bostanci Yakup, Ozden Ender, Akdeniz Ekrem, Kazzazi Amir, Kandemir Bedri, Yakupoglu Yarkin Kamil, Djavan Bob
Departmnet of Urology, New York University School of Medicine, New York, New York 19916, USA.
Can J Urol. 2013 Apr;20(2):6730-3.
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.
原发性睾丸平滑肌肉瘤是一种极其罕见的肿瘤,据我们所知,迄今为止文献中仅报道了20例成人病例。在此,我们报告一例68岁男性患者,其主诉左侧阴囊肿胀2个月。影像学检查显示左侧睾丸肿瘤,无其他器官转移。实施了左侧腹股沟睾丸切除术,组织病理学检查显示为睾丸内平滑肌肉瘤。该患者通过睾丸切除术成功治愈,未接受辅助治疗。在术后12个月的随访期间,疾病无复发或转移。