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Carcinosarcoma and sarcomatoid carcinoma of the bladder: clinicopathological study of 41 cases.

机译:膀胱癌肉瘤和肉瘤样癌:41例临床病理研究。

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PURPOSE: Carcinosarcoma of the bladder is a rare neoplasm characterized by an intimate admixture of carcinoma and malignant soft tissue neoplasm. The clinical usefulness of separating carcinosarcoma (carcinoma with sarcomatous component) from sarcomatoid carcinoma (carcinoma with spindle cell carcinomatous component) is uncertain, and it comprises the subject of this report. MATERIALS AND METHODS: We reviewed the clinical and pathological records of 10 men and 5 women a mean of 66 years old with carcinosarcoma, and 21 men and 5 women a mean of 66.5 years old with sarcomatoid carcinoma of the bladder, as documented in the files of the Mayo Clinic between 1936 and 1995. RESULTS: Of the 15 patients in the carcinosarcoma group 9 had urothelial carcinoma, small cell carcinoma, 3 had squamous cell carcinoma and 2 had more than 1 type. The sarcomatous component included chondrosarcoma in 3 cases, leiomyosarcoma in 3, malignant fibrous histiocytoma in 3, osteosarcoma in 2, fibrosarcoma in 1, rhabdomyosarcoma in 1 and more than 1 type in 2. All disease was high stage at presentation. Treatment included cystectomy in 11 patients with (4) and without (7) radiation therapy, and transurethral resection in 4 with (1) and without (3) radiation therapy. Mean followup available in 14 cases was 34 months (range 1 to 144). A total of 11 patients died of cancer at 1 to 48 months (mean 17.2) and 2 survived for 8 to 131 months. Of the 26 patients in the sarcomatoid carcinoma group 18 had urothelial carcinoma, 1 had squamous carcinoma, 2 had urothelial carcinoma combined with squamous cell carcinoma and 5 had spindle cells only with no recognizable epithelium. All but 1 case was high stage at diagnosis. Treatment included transurethral resection in 17 patients with (7) and without (10) radiation therapy, including 1 who also received chemotherapy, and only cystectomy in 5, including 2 who also underwent radiation therapy and 1 who also received chemotherapy. Mean followup available in 21 cases was 49 months (range 1 to 420). A total of 17 patients died of cancer at 1 to 73 months (mean 9.8), 1 was alive at 140 months and 3 died of unrelated causes. CONCLUSIONS: Carcinosarcoma and sarcomatoid carcinoma of the bladder are highly aggressive malignancies with a similar outcome regardless of histological findings and treatment. Pathological stage is the best predictor of survival.
机译:目的:膀胱癌肉瘤是一种罕见的肿瘤,其特征是癌与恶性软组织肿瘤紧密混合。将癌肉瘤(具有肉瘤成分的癌)与肉瘤样癌(具有梭形细胞癌成分的癌)分离的临床用途尚不确定,这是本报告的主题。材料与方法:我们回顾了10例平均66岁的男性和5名女性患有癌肉瘤,以及21例平均66.5岁的膀胱肉瘤样癌的临床和病理记录,结果:在1936年至1995年期间的梅奥诊所(Mayo Clinic)中。结果:在癌肉瘤组的15例患者中,9例患有尿路上皮癌,小细胞癌,3例患有鳞状细胞癌,2例患有1种以上类型。肉瘤成分包括软骨肉瘤3例,平滑肌肉瘤3例,恶性纤维组织细胞瘤3例,骨肉瘤2例,纤维肉瘤1例,横纹肌肉瘤1例和2型以上。治疗包括11例接受(4)和不接受(7)放射治疗的患者的膀胱切除术,以及经尿道切除术的4接受(1)和不接受(3)放射治疗的患者。 14例患者的平均随访时间为34个月(范围1至144)。共有11名患者在1至48个月内死于癌症(平均17.2),其中2例存活了8至131个月。在肉瘤样癌组的26例患者中,18例患有尿路上皮癌,1例患有鳞状癌,2例患有尿路上皮癌合并鳞状细胞癌,5例仅具有梭形细胞且无可辨认的上皮细胞。除1例外,其他所有病例均在诊断中处于晚期。治疗包括对17例接受(7)和不采用(10)放射治疗的患者行经尿道切除术,其中1例也接受了化疗,只有5例行膀胱切除术,其中2例也接受了放射治疗,1例也接受了化疗。 21例患者的平均随访时间为49个月(范围1至420)。共有17例患者在1到73个月时死于癌症(平均9.8),1例在140个月时还活着,而3例则死于无关原因。结论:膀胱癌肉瘤和肉瘤样癌是高度侵袭性的恶性肿瘤,无论组织学表现和治疗如何,其恶性程度均相似。病理阶段是生存的最佳预测指标。

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