Baba Tokuro, Hamada Satoru, Sakiyama Hideki, Kiyuna Shinobu, Oshioro Tokiko, Kuda Masaaki, Ieiri Satoshi, Takatsuki Mitsuhisa
Department of Digestive and General Surgery, Graduate School of Medicine, University of the Ryukyus, Kiyuna, Ginowan, Japan.
Department of Child Health and Welfare, Graduate School of Medicine, University of the Ryukyus, Kiyuna, Ginowan, Japan.
Asian J Endosc Surg. 2025 Jan-Dec;18(1):e70064. doi: 10.1111/ases.70064.
Neuroblastoma, typically presenting with atypical symptoms, rarely manifests as a urachal tumor. We report a case of urachal neuroblastoma wherein a single port site was used for both laparotomy and thoracoscopy. A 1-month-old female presented with umbilical discharge. Enhanced computed tomography revealed a urachal tumor, later confirmed pathologically as neuroblastoma without MYCN amplification. During chemotherapy for low-risk classification, a right adrenal mass and mediastinal lymphadenopathy emerged, prompting further biopsy. We employed a port-sharing procedure at the right hypochondrium to perform simultaneous laparoscopic and thoracoscopic biopsies, reducing the number of port-side wounds. This approach could be applicable in other cases requiring combined thoracic and abdominal surgical access.
神经母细胞瘤通常表现为非典型症状,很少表现为脐尿管肿瘤。我们报告一例脐尿管神经母细胞瘤病例,其中单一端口部位用于剖腹手术和胸腔镜检查。一名1个月大的女性出现脐部渗液。增强计算机断层扫描显示脐尿管肿瘤,病理检查后来证实为无MYCN扩增的神经母细胞瘤。在针对低风险分类的化疗期间,出现了右肾上腺肿块和纵隔淋巴结病,促使进一步活检。我们在右季肋部采用端口共享程序进行同步腹腔镜和胸腔镜活检,减少了端口侧伤口的数量。这种方法可能适用于其他需要联合胸腹部手术入路的病例。