转移至膀胱:肾细胞癌复发的罕见部位。

Case Reports in Urology Pub Date : 2022-06-17 eCollection Date: 2022-01-01 DOI:10.1155/2022/4339270
Amanda Smart, Michael Wynne, Ezra Baraban, Yasser Ged, Armine Smith
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引用次数: 0

摘要

肾细胞癌(RCC)被认为是最致命的泌尿系统癌症,肾切除术后的转移率和复发率都很高。RCC 几乎可以转移到任何器官,但最常见的是转移到肝、肺、脑和骨。迄今为止,仅有约 40 例 RCC 单发膀胱转移的报道。以下报告为这一有限的数据集做出了贡献:RCC 患者单发转移至膀胱。一名 69 岁的男性患者出现偶发性毛细血尿,发现左肾肿块浸润集合系统。输尿管镜活检显示患者为透明细胞 RCC,随后患者接受了左肾根治性切除术。肾切除术后八个月,患者因严重血尿就诊。诊室膀胱镜检查显示,膀胱内的结节性病变来自左侧输尿管口。患者接受了经尿道膀胱肿块切除术,病理结果显示为透明细胞型红斑狼疮。随后的影像学检查未发现转移性疾病。经尿道切除术五个月后,患者被发现左侧输尿管远端有肿块,于是接受了左侧输尿管切除术和部分膀胱切除术。病理再次显示为透明细胞 RCC。单发转移至膀胱的 RCC 比较罕见,目前还没有针对性的治疗指南建议。根据治疗标准,有无痛性血尿和恶性肿瘤危险因素的患者应接受膀胱镜检查。对于有 RCC 病史的患者,在鉴别诊断时应考虑膀胱转移。RCC转移至膀胱的患者应进行全面检查,以确定是否有其他转移部位。对于在肾切除术后出现可进行切除的单发膀胱转移瘤的 RCC 患者,目前缺乏指导治疗的证据,因此需要进行多学科讨论。不过,如果肿瘤可以切除,转移灶切除术是一种合理的治疗方法,可提高患者的生活质量,并为病情缓解提供机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma.

Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma.

Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma.

Metastasis to the Bladder: A Rare Site of Recurrence of Renal Cell Carcinoma.

Renal cell carcinoma (RCC) is considered to be the deadliest urologic cancer with high rates of metastasis and recurrence after nephrectomy. RCC can metastasize to nearly any organ but most commonly metastasizes to the liver, lung, brain, and bone. To date, there are only about 40 reported cases of RCC with solitary bladder metastasis. The following report contributes to this limited data set of patients with RCC who develop solitary metastasis to the bladder. A 69-year-old male presented with occasional gross hematuria and was found to have a left renal mass infiltrating the collecting system. Ureteroscopic biopsy revealed clear cell RCC, and the patient subsequently underwent radical left nephrectomy. Eight months after nephrectomy, the patient presented to the clinic with gross hematuria. In-office cystoscopy demonstrated a nodular lesion in the bladder arising from the left ureteral orifice. The patient underwent transurethral resection of the bladder mass and pathology demonstrated clear cell RCC. Subsequent imaging showed no evidence of metastatic disease. Five months after transurethral resection, the patient was found to have a left distal ureteral mass and underwent left ureterectomy with partial cystectomy. Pathology again demonstrated clear cell RCC. RCC with solitary metastasis to the bladder is rare, and there are no targeted guideline recommendations for management. Per standard of care, patients with painless hematuria and risk factors for malignancy should undergo cystoscopy. In patients with a history of RCC, metastasis to the bladder should be considered in the differential diagnosis. Patients with metastatic RCC to the bladder should undergo a thorough work-up for additional sites of metastasis. In patients with RCC who develop solitary bladder metastasis amenable to resection following nephrectomy, there is a lack of evidence to guide therapy and a multidisciplinary discussion is warranted. However, if the tumor is amenable to resection, metastasectomy is a reasonable therapeutic approach and offers the patient an improved quality of life and an opportunity for remission.

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