Griffin J H, Waters W B
Department of Urology, Loyola University Medical Center, Maywood, Illinois 60153, USA.
J Surg Oncol. 1996 Jun;62(2):148-52. doi: 10.1002/(SICI)1096-9098(199606)62:2<148::AID-JSO13>3.0.CO;2-4.
We report the thirteenth case of primary leiomyosarcoma of the ureter, as well as a summary of previous cases. It is the first case reported to be studied by computer tomography and immunohistochemical procedure. Further evaluation included intravenous pyelogram, cystoscopy with retrograde pyelogram, cell block for cytology, and electron microscopy. Leiomyosarcoma is a very rare disease that is difficult to diagnose. It has a very poor 5-year disease-specific survival.
我们报告了输尿管原发性平滑肌肉瘤的第13例病例，并对既往病例进行了总结。这是首例通过计算机断层扫描和免疫组织化学方法进行研究的病例。进一步评估包括静脉肾盂造影、膀胱镜检查及逆行肾盂造影、细胞块细胞学检查和电子显微镜检查。平滑肌肉瘤是一种非常罕见且难以诊断的疾病。其5年疾病特异性生存率非常低。
