Suppr超能文献

[膀胱肉瘤样尿路上皮癌,包括骨肉瘤成分]

[Sarcomatoid Urothelial Carcinoma of the Bladder Including an Osteosarcoma Element].

作者信息

Tanuma Kouzaburou, Kawai Koji, Tsuchiya Haruki, Matsumoto Yoshitaka, Kandori Shuya, Kojima Takahiro, Kimura Tomokazu, Joraku Akira, Miyazaki Jun, Nishiyama Hiroyuki, Sakata Akiko

机构信息

The Department of Urology, Faculty of Medicine, University of Tsukuba.

The Department of Pathology, Hitachi General Hospital.

出版信息

Hinyokika Kiyo. 2017 Nov;63(11):487-492. doi: 10.14989/ActaUrolJap_63_11_487.

Abstract

A 68-year-old Japanese man was referred to Tsukuba University Hospital for bladder cancer treatment. He had undergone a transurethral resection of a bladder tumor (TURBT) at a local hospital, but the pathological specimen did not contain muscle layer. Abdominal computed tomography (CT) and magnetic resonance imaging revealed a 3 cm non-papillary bladder tumor with muscle invasion, but there was no apparent calcification. The patient underwent re-TURBT at our hospital for diagnosis and staging. A non-papillary pedunculated tumor was identified in the bladder dome, and it contained a small papillary part. The non-papillary part was stony hard and difficult to cut with electrocautery, whereas the small papillary part was easily cut. Histologically, the non-papillary part was composed of sarcomatous elements including osteosarcoma, chondrosarcoma, and spindle cell sarcoma. The papillary part was composed of high-grade urothelial carcinoma and spindle cell sarcoma. Muscularis propria was not present in the specimen. Since the staging study with CT was negative for metastases, we performed a total cystectomy with an ileal conduit under the clinical diagnosis of muscle-invasive sarcomatoid urothelial carcinoma. The pathological findings were identical to those of the re-TURBT specimens, and our diagnosis was pTxN0 sarcomatoid urothelial carcinoma. The patient received adjuvant chemotherapy with two courses of gemcitabine and cisplatin. There was neither recurrence nor metastases during the 20-month follow-up. Reports of sarcomatoid urothelial carcinoma of the bladder with an osteosarcoma element are rare, and only eight other cases hane been reported in the Japanese literature.

摘要

一名68岁的日本男性因膀胱癌治疗被转诊至筑波大学医院。他曾在当地医院接受经尿道膀胱肿瘤切除术(TURBT),但病理标本中未包含肌层。腹部计算机断层扫描(CT)和磁共振成像显示一个3厘米的非乳头状膀胱肿瘤伴肌层浸润,但未见明显钙化。患者在我院接受再次TURBT以进行诊断和分期。在膀胱顶部发现一个非乳头状带蒂肿瘤,其中包含一个小的乳头状部分。非乳头状部分质地坚硬如石,用电灼难以切割,而小的乳头状部分则易于切割。组织学上,非乳头状部分由包括骨肉瘤、软骨肉瘤和梭形细胞肉瘤在内的肉瘤成分组成。乳头状部分由高级别尿路上皮癌和梭形细胞肉瘤组成。标本中未见固有肌层。由于CT分期检查未发现转移,我们在临床诊断为肌层浸润性肉瘤样尿路上皮癌的情况下进行了全膀胱切除术并回肠代膀胱术。病理结果与再次TURBT标本相同,我们的诊断为pTxN0肉瘤样尿路上皮癌。患者接受了两疗程吉西他滨和顺铂的辅助化疗。在20个月的随访期间既无复发也无转移。膀胱肉瘤样尿路上皮癌伴骨肉瘤成分的报道罕见,日本文献中仅另有8例报道。

相似文献

7
[A case report of sarcomatoid carcinoma of the urinary bladder].[一例膀胱肉瘤样癌的病例报告]
Nihon Hinyokika Gakkai Zasshi. 2007 Mar;98(3):576-9. doi: 10.5980/jpnjurol1989.98.576.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验