Demir Aslan, Yazici Cenk M, Eren Funda, Türkeri Levent
Department of Urology, Marmara University School of Medicine, Marmara University Hospital, Altunizade, Istanbul, Turkey.
Int Urol Nephrol. 2007;39(1):7-10. doi: 10.1007/s11255-005-4025-4.
Sarcomas represent 1-2% of all malignant renal tumors in adults, with an incidence that increases with advancing age. Renal sarcoma is less common, but more lethal than sarcoma of any other genitourinary site. The common signs and symptoms associated with renal sarcoma in adults include palpable mass, abdominal or flank pain and hematuria similar to those seen with large, rapidly growing renal cell carcinomas. Usually, radical nephrectomy remains the treatment of choice for these tumors, which exhibits an aggressive biological behavior and an unfavorable prognosis. We describe an unusual case of renal leiomyosarcoma that underwent nephron sparing surgery, in a 55-year-old white woman, who had a renal mass for 3 years. The size of the renal mass did not change during this period and no distant metastasis occurred. The patient is still alive without any symptoms of relapse.
肉瘤占成人所有恶性肾肿瘤的1%-2%,其发病率随年龄增长而增加。肾肉瘤较为少见,但比其他任何泌尿生殖部位的肉瘤更具致命性。成人肾肉瘤的常见体征和症状包括可触及的肿块、腹部或侧腹疼痛以及血尿,与大型、快速生长的肾细胞癌所见症状相似。通常,根治性肾切除术仍是这些肿瘤的首选治疗方法,这些肿瘤表现出侵袭性生物学行为和不良预后。我们描述了一例不寻常的肾平滑肌肉瘤病例,该病例为一名55岁白人女性,患有肾肿块3年,接受了保留肾单位手术。在此期间,肾肿块大小未变,也未发生远处转移。患者仍存活,无任何复发症状。