Tsuji Kentaro, Ito Atsushi, Kurokawa Shinsuke, Nakaya Takeo, Yoshimoto Taichiro, Kawata Hirotoshi, Tamba-Sakaguchi Mio, Fukushima Noriyoshi, Oshiro Hisashi
Department of Diagnostic Pathology, Jichi Medical University Hospital.
Department of Urology, Jichi Medical University School of Medicine, Shimotsuke, Tochigi, Japan.
Medicine (Baltimore). 2019 Aug;98(32):e16643. doi: 10.1097/MD.0000000000016643.
Primary carcinosarcoma of the upper urinary tract is rare. Ureteral duplication is one of the most common urinary tract malformations. Additionally, the association between ureteral duplication and malignancy is unknown. To the best of our knowledge, no cases of malignant tumors diagnosed as carcinosarcoma with ureteral duplication have been reported. We herein report the case of a patient with carcinosarcoma of the ureteropelvic junction associated with incomplete ureteral duplication.
A 60-year-old Japanese woman presented with painless gross hematuria. She had a history of total hysterectomy and chemotherapy for endometrioid carcinoma 5 years before. She had no history of occupational chemical exposure.
Radiographic imaging revealed right incomplete ureteral duplication, hydronephrosis, and a polypoid tumor in the ureteropelvic junction of the lower moiety of the right kidney. Urine cytology showed a small amount of degenerated atypical epithelial and nonepithelial cells. The transureteral biopsy specimen showed dysplastic urothelial cells and atypical myoid spindle cells. These findings were indefinite for malignancy.
The patient underwent right nephroureterectomy. Pathological examination of the resected tumor showed a biphasic neoplasm composed of carcinomatous and sarcomatous components. The sarcomatous component was immunohistochemically positive for vimentin, desmin, h-caldesmon, and α-SMA and negative for pancytokeratin (AE1/AE3), low molecular weight cytokeratin (CAM 5.2), EMA, E-cadherin, GATA3, uroplakin 2, and p63. Based on these findings, we diagnosed the tumor as carcinosarcoma.
The postoperative course was uneventful. No additional therapy was administered. The patient has remained alive without recurrence for 21 months since surgery.
Carcinosarcoma can arise from ureteral duplication. Although the majority of carcinosarcomas of the upper urinary tract are diagnosed at an advanced stage and have a poor prognosis, some can have a less aggressive course. Further studies are needed to determine the association between ureteral duplication and malignancy.
上尿路原发性癌肉瘤罕见。输尿管重复畸形是最常见的泌尿系统畸形之一。此外,输尿管重复畸形与恶性肿瘤之间的关联尚不清楚。据我们所知,尚未有诊断为癌肉瘤且伴有输尿管重复畸形的恶性肿瘤病例报道。我们在此报告一例输尿管肾盂交界处癌肉瘤合并不完全性输尿管重复畸形的患者。
一名60岁的日本女性,表现为无痛性肉眼血尿。她5年前有子宫内膜样癌全子宫切除及化疗史。她无职业化学物质接触史。
影像学检查显示右侧不完全性输尿管重复畸形、肾积水,右肾下部分输尿管肾盂交界处有一息肉样肿瘤。尿细胞学检查显示少量退变的非典型上皮细胞和非上皮细胞。经输尿管活检标本显示发育异常的尿路上皮细胞和非典型肌样梭形细胞。这些发现不能明确为恶性肿瘤。
患者接受了右侧肾输尿管切除术。切除肿瘤的病理检查显示为一种双相性肿瘤,由癌性和肉瘤性成分组成。肉瘤性成分免疫组化显示波形蛋白、结蛋白、h - 钙调蛋白和α - 平滑肌肌动蛋白阳性,而全细胞角蛋白(AE1/AE3)、低分子量细胞角蛋白(CAM 5.2)、上皮膜抗原、E - 钙黏蛋白、GATA3、尿桥蛋白2和p63阴性。基于这些发现,我们将肿瘤诊断为癌肉瘤。
术后过程顺利。未给予额外治疗。自手术以来,患者已存活21个月,无复发。
癌肉瘤可起源于输尿管重复畸形。虽然大多数上尿路癌肉瘤在晚期被诊断,预后较差,但有些可能病程侵袭性较小。需要进一步研究以确定输尿管重复畸形与恶性肿瘤之间的关联。