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经 TURP 诊断的前列腺尿道原发性黏液产生型尿路上皮型腺癌:病例报告及文献复习。

Primary mucin-producing urothelial-type adenocarcinoma of the prostatic urethra diagnosed on TURP: a case report and review of literature.

机构信息

Columbia University College of Physicians and Surgeons, 630 W, 168th St, New York, NY 10032, USA.

出版信息

BMC Urol. 2014 May 22;14:39. doi: 10.1186/1471-2490-14-39.

Abstract

BACKGROUND

Mucin-producing urothelial-type adenocarcinoma of the prostatic urethra is extremely rare. These lesions must be differentiated from other mucinous tumors including mucin-producing prostatic adenocarcinoma and metastases from either colonic or bladder primaries.

CASE PRESENTATION

We report here a case of urothelial-type adenocarcinoma arising from the prostatic urethra. The patient is an 81 year-old man with a history of pT1 urothelial cell carcinoma of the bladder status post trans-urethral resection of bladder tumor (TURBT) who initially presented with irritative lower urinary tract symptoms and mucosuria refractory to Flomax and finasteride. A shared decision was made for the patient to undergo trans-urethral resection of prostate (TURP). At the time of surgery, a papillary tumor emanating from the prostatic urethra was found and no urothelial lesions were noted in the bladder. Pathology of the resected prostatic chips revealed an invasive adenocarcinoma with intestinal-type differentiation that stained positive for CK7, CK20, and villin, but negative for PSA, PSAP, uroplakin, and CDX-2. Colonoscopy was normal and CT scan did not show any evidence of colonic lesions nor visceral or lymph node metastases. Thus, the patient was diagnosed with a primary urothelial-type adenocarcinoma of the prostatic urethra.

CONCLUSION

Herein we review the literature regarding this unusual entity, and discuss the differential diagnosis, immunohistochemistry, and the importance of correctly identifying this rare tumor.

摘要

背景

前列腺尿道的黏液产生型尿路上皮样腺癌极为罕见。这些病变必须与其他黏液性肿瘤区分开来,包括黏液产生型前列腺腺癌和结直肠或膀胱原发肿瘤的转移。

病例介绍

我们在此报告一例源自前列腺尿道的尿路上皮样腺癌。患者为 81 岁男性,有膀胱移行细胞癌病史,曾行经尿道膀胱肿瘤切除术(TURBT),最初表现为刺激性下尿路症状和黏液尿,Flomax 和非那雄胺治疗无效。患者与医生共同决定行经尿道前列腺切除术(TURP)。手术时发现从前列腺尿道发出的乳头状肿瘤,膀胱无尿路上皮病变。切除的前列腺组织芯片病理显示为具有肠型分化的浸润性腺癌,CK7、CK20 和 villin 阳性,但 PSA、PSAP、uroplakin 和 CDX-2 阴性。结肠镜检查正常,CT 扫描未显示结肠病变或内脏或淋巴结转移。因此,患者被诊断为原发性前列腺尿道尿路上皮样腺癌。

结论

本文回顾了关于这种罕见实体的文献,并讨论了鉴别诊断、免疫组织化学以及正确识别这种罕见肿瘤的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bade/4059493/fa1f49a741c8/1471-2490-14-39-1.jpg

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