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膀胱癌肉瘤及肉瘤样癌:41例临床病理研究

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

作者信息

Lopez-Beltran A, Pacelli A, Rothenberg H J, Wollan P C, Zincke H, Blute M L, Bostwick D G

机构信息

Department of Pathology, Cordoba University Medical School, Spain.

出版信息

J Urol. 1998 May;159(5):1497-503. doi: 10.1097/00005392-199805000-00023.

Abstract

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.

摘要

目的

膀胱癌肉瘤是一种罕见的肿瘤,其特征是癌组织与恶性软组织肿瘤紧密混合。将癌肉瘤(伴有肉瘤成分的癌)与肉瘤样癌(伴有梭形细胞癌成分的癌)区分开来的临床实用性尚不确定,这也是本报告的主题。

材料与方法

我们回顾了梅奥诊所1936年至1995年档案中记录的10例男性和5例女性平均年龄66岁的癌肉瘤患者,以及21例男性和5例女性平均年龄66.5岁的膀胱肉瘤样癌患者的临床和病理记录。

结果

癌肉瘤组的15例患者中,9例为尿路上皮癌、小细胞癌,3例为鳞状细胞癌,2例有不止一种类型。肉瘤成分包括3例软骨肉瘤、3例平滑肌肉瘤、3例恶性纤维组织细胞瘤、2例骨肉瘤、1例纤维肉瘤、1例横纹肌肉瘤,2例有不止一种类型。所有病例初诊时均为晚期。治疗方法包括11例患者行膀胱切除术(4例接受放疗,7例未接受放疗),4例患者行经尿道切除术(1例接受放疗,3例未接受放疗)。14例患者的平均随访时间为34个月(范围1至144个月)。共有11例患者在1至48个月(平均17.2个月)死于癌症,2例存活8至131个月。肉瘤样癌组的26例患者中,18例为尿路上皮癌,1例为鳞状癌,2例为尿路上皮癌合并鳞状细胞癌,5例仅为梭形细胞,无明显上皮成分。除1例病例外,所有病例诊断时均为晚期。治疗方法包括17例患者行经尿道切除术(7例接受放疗,10例未接受放疗,其中1例还接受了化疗),5例患者仅行膀胱切除术(2例还接受了放疗,1例还接受了化疗)。21例患者的平均随访时间为49个月(范围1至420个月)。共有17例患者在1至73个月(平均9.8个月)死于癌症,1例在140个月时存活,3例死于无关原因。

结论

膀胱癌肉瘤和肉瘤样癌是侵袭性很强的恶性肿瘤,无论组织学表现和治疗方法如何,预后相似。病理分期是生存的最佳预测指标。

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