Cartagena Kenneth Cintrón, Colón Gustavo Christian, Pérez Merary Nazario, Matta Jaime, Parachini Adrian Santana, Ortiz Javier Castillo
St. Luke's Hospital Urology Residency, 917 Av. Tito Castro, Ponce 00733, Puerto Rico; Ponce Health Sciences University Department of Surgery, Sala Ponce, 388 Calle Luis F, Ponce 00716, Puerto Rico.
Ponce Health Sciences University School of Medicine, Sala Ponce, 388 Calle Luis F, Ponce 00716, Puerto Rico.
Int J Surg Case Rep. 2025 Jun;131:111300. doi: 10.1016/j.ijscr.2025.111300. Epub 2025 Apr 18.
Merkel cell carcinoma (MCC) is a rare, aggressive neuroendocrine skin cancer with a high propensity for metastasis. While MCC has been reported in various organs, its metastasis to the bladder is exceedingly uncommon. Bladder infiltration in MCC presents a unique diagnostic and therapeutic challenge in Urology. Only few have been described worldwide, and no cases have been reported in Hispanic males. This is the first published case of an immunocompromised Hispanic patient with MCC metastasis to the bladder and to our knowledge, the first case report worldwide to include narrowband imaging (NBI) in the diagnostic algorithm of MCC to the bladder.
We report the case of a 53-year-old immunocompromised Puerto Rican male diagnosed with metastatic MCC. The patient had previously developed MCC with metastasis to the inguinal lymph nodes and received treatment. Later management involved immunotherapy once node persistence was found. Recent investigation revealed a new metastasis to the urinary bladder, presenting with gross hematuria. Diagnostic evaluation included computed tomography (CT) and Cystoscopy with white light and NBI, which confirmed the bladder metastasis. The patient underwent transurethral resection of the bladder tumor (TURBT) for tissue diagnosis. This work has been reported in line with the SCARE criteria (Sohrabi et al., 2023).
Histopathological analysis confirmed the diagnosis of metastatic MCC to the urinary bladder. The patient was managed with nephrostomy tube placement for obstructive uropathy and further immunotherapy for metastatic disease. Despite intervention, the prognosis remains poor due to the aggressive nature of the tumor and the patient's immunocompromised state.
This case highlights the unusual presentation of MCC with bladder metastasis in an immunocompromised Hispanic male. The patient revealed aggressive pathology per CT and developed persistent hematuria which were managed with bilateral nephrostomy for symptom relief. To our knowledge, this is the first reported case of MCC bladder metastasis in a Puerto Rican immunocompromised male, underscoring the importance of considering rare metastatic sites in MCC and tailoring treatment approaches accordingly.
默克尔细胞癌(MCC)是一种罕见的、侵袭性神经内分泌皮肤癌,具有较高的转移倾向。虽然MCC已在多个器官中被报道,但其转移至膀胱极为罕见。MCC浸润膀胱给泌尿外科带来了独特的诊断和治疗挑战。全球仅有少数病例被描述,且尚无西班牙裔男性病例的报道。这是首例免疫功能低下的西班牙裔患者发生MCC转移至膀胱的病例报告,据我们所知,也是全球首例在MCC膀胱转移诊断算法中纳入窄带成像(NBI)的病例报告。
我们报告一例53岁免疫功能低下的波多黎各男性患者,诊断为转移性MCC。该患者此前已发生MCC并转移至腹股沟淋巴结,接受过治疗。后来发现淋巴结持续存在时进行了免疫治疗。近期检查发现新的膀胱转移,表现为肉眼血尿。诊断评估包括计算机断层扫描(CT)以及白光和NBI膀胱镜检查,证实了膀胱转移。患者接受了经尿道膀胱肿瘤切除术(TURBT)以进行组织诊断。本病例报告遵循SCARE标准(Sohrabi等人,2023年)。
组织病理学分析确诊为膀胱转移性MCC。患者因梗阻性肾病接受了肾造瘘管置入术,并针对转移性疾病接受了进一步的免疫治疗。尽管进行了干预,但由于肿瘤具有侵袭性以及患者免疫功能低下,预后仍然较差。
本病例突出了免疫功能低下的西班牙裔男性MCC发生膀胱转移的不寻常表现。患者CT显示侵袭性病理特征,并出现持续性血尿,通过双侧肾造瘘术缓解症状。据我们所知,这是首例波多黎各免疫功能低下男性患者发生MCC膀胱转移的病例报告,强调了考虑MCC罕见转移部位并相应调整治疗方法的重要性。