Urothelial carcinoma with trophoblastic differentiation: case report and review of literature.

Q2 Medicine
Medicine and Pharmacy Reports Pub Date : 2026-07-01 Epub Date: 2026-07-30 DOI:10.15386/mpr-3002
Bogdan-Petru Tichil, Patricia Inisca, Adelina Gheju, Bogdan Fetica, Anamaria Besleaga, Mihaela Laura Vica, Adrian Florea
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Abstract

Urothelial carcinoma with trophoblastic differentiation (UCTD) is a rare histological variant of urothelial carcinoma characterized by the presence of trophoblastic elements and expression of β-human chorionic gonadotropin (β-hCG). Published evidence is limited, and the clinical behavior of this variant remains incompletely understood. The objective of this study is to review the available literature regarding the incidence, clinicopathological characteristics, treatment modalities, recurrence patterns, survival outcomes, and prognostic implications and to present the case of a patient with UCTD. A 66-year-old male patient presented in February 2025 with a 2-month history of progressive left inguinal swelling and recurrent left hydrocele. Past medical history revealed: radical cystectomy with ileal neobladder, pelvic lymphadenectomy (for bladder pT2G3 recurrent BCG resistant bladder tumor) performed on the 28th of June 2018. Full body contrast CT scan had been performed on the 24th of December 2024 and revealed a left inguinal adenopathy conglomerate 9.93 cm in length, with the largest lymph node measuring 2.5 cm, bilateral peritesticular fluid collections (hydrocele) with no evidence of local tumor recurrence in the neobladder or prostate bed and a supradiaphragmatic, calcified pleural mass (3.4 × 1.8 cm). Scrotal ultrasound revealed: large bilateral hydrocele, left epididymal and upper testicular pole tumor (~2 cm in size) with increased Doppler vascularity and a large left inguinal adenopathy conglomerate (~10 cm in size) with increased Doppler vascularity. Testicular cancer serum markers were performed and a serum β-hCG of 5893 mIU/ml, was found. Ultrasonographical assessment and positive testicular cancer biomarkers prompted us to suspect a testicular tumor with inguinal lymph node metastases. Patient was referred for surgery. Left inguinal radical orchidectomy was performed along with left inguinal lymphadenectomy. Histopathological examination of the testicle revealed testicular and epididymal inflammation. Lymph node examination revealed urothelial carcinoma with squamous and trophoblastic differentiation, PDL1(22C3) positive, CK7 positive, GATA3 positive, CK20 positive, p16 negative and beta HCG positive on 10% of cells. Patient was started on platinum-based chemotherapy with rapid disease progression and died of metastatic complications approximately 11 months after the initial recurrence signs were visible on the CT scan.

Conclusions: UCTD is a rare and aggressive variant of urothelial carcinoma associated with unfavorable oncological outcomes. Available evidence supports aggressive treatment and prolonged follow-up. To our knowledge, this may represent one of the few reported, very late recurrences after radical cystectomy.

尿路上皮癌伴滋养细胞分化:1例报告及文献复习。
尿路上皮癌伴滋养细胞分化(UCTD)是一种罕见的尿路上皮癌的组织学变异,其特征是存在滋养细胞因子和β-人绒毛膜促性腺激素(β-hCG)的表达。已发表的证据有限,这种变异的临床行为仍然不完全清楚。本研究的目的是回顾关于发病率、临床病理特征、治疗方式、复发模式、生存结果和预后影响的现有文献,并介绍一例UCTD患者。一名66岁男性患者于2025年2月就诊,有2个月进行性左腹股沟肿胀和复发性左侧鞘膜积液病史。既往病史:2018年6月28日行根治性膀胱切除术伴回肠新生膀胱,盆腔淋巴结切除术(用于膀胱pT2G3复发性卡介苗耐药膀胱肿瘤)。2024年12月24日行全身CT扫描,发现左侧腹股沟腺瘤,长9.93 cm,最大淋巴结2.5 cm,双侧睾丸周围积液(鞘膜积液),未见新膀胱或前列腺床局部肿瘤复发,膈上胸膜钙化肿块(3.4 × 1.8 cm)。阴囊超声示:双侧大鞘膜积液,左侧附睾及睾丸上极肿瘤(约2cm)伴多普勒血管增强,左侧腹股沟大腺瘤(约10cm)伴多普勒血管增强。检测睾丸癌血清标志物,血清β-hCG为5893 mIU/ml。超声检查和阳性的睾丸癌生物标志物提示我们怀疑睾丸肿瘤合并腹股沟淋巴结转移。病人被转介做手术。左侧腹股沟根治性睾丸切除术与左侧腹股沟淋巴结切除术同时进行。睾丸组织病理学检查显示睾丸和附睾炎症。淋巴结检查显示尿路上皮癌呈鳞状和滋养细胞分化,10%的细胞PDL1(22C3)阳性,CK7阳性,GATA3阳性,CK20阳性,p16阴性,β HCG阳性。患者开始接受以铂为基础的化疗,病情进展迅速,在CT扫描显示初始复发迹象约11个月后死于转移性并发症。结论:UCTD是一种罕见且侵袭性的尿路上皮癌变体,与不良的肿瘤预后相关。现有证据支持积极治疗和长期随访。据我们所知,这可能是根治性膀胱切除术后极少报道的晚期复发病例之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicine and Pharmacy Reports
Medicine and Pharmacy Reports Medicine-Medicine (all)
CiteScore
3.10
自引率
0.00%
发文量
63
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