An Unusual Location for a Nonurachal Bladder Adenocarcinoma.

Case Reports in Urology Pub Date : 2021-09-23 eCollection Date: 2021-01-01 DOI:10.1155/2021/5827120
George Khludenev, Akshay Reddy, Sinan Akosman, Michael J Whalen
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Abstract

Malignant bladder neoplasms represent a significant disease burden not only for urologists but also the broader medical community. While the majority of bladder tumors are urothelial in origin, up to two percent are found to be adenocarcinomas. Among bladder adenocarcinomas, roughly one-tenth are urachal and are frequently located at the dome of the bladder where urachal remnants can often be found. We describe a case of bladder adenocarcinoma that presented at the dome of the bladder but ultimately exhibited a nonurachal histology. A 65-year-old male with a history of myocardial infarction and cerebrovascular accident with residual right-sided hemiparesis and aphasia was referred to our clinic for evaluation of a bladder mass discovered in the setting of painless gross hematuria. Diagnostic cystoscopy demonstrated a large mass at the dome of the bladder, and subsequent transurethral resection revealed stage T1 mucinous adenocarcinoma arising in a villous adenomatous lesion without the presence of muscle in the specimen. The patient underwent a robotic-assisted laparoscopic partial cystectomy with extended bilateral pelvic lymph node dissection. Postoperatively, the patient experienced short-lived paralytic ileus and was discharged on postoperative day 5. Follow-up surveillance imaging at 6 months with CT chest, abdomen, and pelvis, repeat office cystoscopy, and negative tumor markers postoperatively indicated no evidence of disease recurrence. Characterization of bladder adenocarcinomas into urachal and nonurachal subtypes is critical in differentiating the operative management and oncologic outcomes of the respective neoplasms. However, given the paucity of literature describing treatment approaches to bladder adenocarcinoma in general, existing methods have largely mirrored genetically similar neoplasms, including ovarian and colon adenocarcinomas. Although there is still much to be understood regarding the potential mechanisms of carcinogenesis of nonurachal adenocarcinomas, further investigation may pave the way for a more standardized treatment paradigm and provide insight into the potential utility of modern immunotherapies.

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非尿管膀胱腺癌的异常部位。
恶性膀胱肿瘤不仅是泌尿科医生的重要疾病负担,也是更广泛的医学界的负担。虽然大多数膀胱肿瘤起源于尿路上皮,但高达2%的肿瘤是腺癌。在膀胱腺癌中,大约十分之一是尿管癌,并且经常位于膀胱穹窿,在那里经常可以发现尿管残余。我们描述了一例膀胱腺癌,在膀胱穹窿出现,但最终表现为非尿管组织学。一位65岁男性患者,有心肌梗死及脑血管意外病史,并伴有右侧偏瘫及失语,因无痛性肉眼血尿发现膀胱肿块而被转介至本诊所。诊断性膀胱镜检查显示膀胱穹部有一个大肿块,随后经尿道切除术显示T1期粘液腺癌出现在绒毛状腺瘤病变中,标本中没有肌肉存在。患者接受了机器人辅助的腹腔镜部分膀胱切除术和扩大的双侧盆腔淋巴结清扫。术后患者出现短暂麻痹性肠梗阻,于术后第5天出院。随访6个月的胸部、腹部和骨盆CT、复查膀胱镜检查和术后阴性肿瘤标志物显示无疾病复发迹象。将膀胱腺癌分为尿管和非尿管亚型是区分不同肿瘤的手术处理和肿瘤预后的关键。然而,由于缺乏文献描述膀胱腺癌的治疗方法,现有的方法在很大程度上反映了基因相似的肿瘤,包括卵巢和结肠腺癌。尽管关于非尿路腺癌的潜在致癌机制仍有很多有待了解的地方,但进一步的研究可能为更标准化的治疗模式铺平道路,并为现代免疫疗法的潜在效用提供见解。
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审稿时长
13 weeks
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