Sabaté-Ortega Josep, Albert-Carrasco Marc, Escribano-Ferrer Carmen, Grau-Manrubia Gerard, Fina-Planas Clàudia, López-Núñez Carme, Teixidor-Vilà Eduard, Bujons-Buscarons Elisabet, Montañés-Ferrer Clàudia, Sala-González Núria
Department of Medical Oncology, Catalan Institute of Oncology, Doctor Josep Trueta University Hospital, Girona, Spain.
Precision Oncology Group (OncoGIR-Pro), Girona Biomedical Research Institute (IDIBGI-CERCA), Parc Hospitalari Martí i Julià, Salt, Spain.
Front Oncol. 2024 May 2;14:1354127. doi: 10.3389/fonc.2024.1354127. eCollection 2024.
Renal cell carcinoma (RCC) is a kidney neoplasm that accounts for 85% of cases and has complex genetic pathways that affect its development and progression. RCC metastasis can occur in 20%-50% of patients and usually affects distant organs. Gastric metastases (GM) from RCC are rare and present as polyp-like growths in the submucosal layer, accounting for 0.2%-0.7% of cases. This case report describes an 84-year-old female with Furhman grade II ccRCC who presented with an atherothrombotic ischemic stroke and gastrointestinal bleeding nine years post-radical nephrectomy. Gastroscopy revealed a 12mm pseudopedicled gastric lesion with ulceration and bleeding, diagnosed as metastatic ccRCC. The discussion focuses on the rarity, diagnostic challenges, and prognostic elements of gastric metastasis from RCC. The median survival after detecting digestive metastasis varies widely, and the mechanisms include direct invasion and dissemination through lymphatic, transcelomic, or hematogenous routes. Prognostic markers encompass patient history, symptoms, time since RCC diagnosis, overall health, and genetic factors. Surgical removal of gastric lesions and targeted therapy are treatment options that can improve survival. This case report highlights the need for further research to enhance diagnostic and treatment strategies for this rare aspect of RCC pathophysiology.
肾细胞癌(RCC)是一种肾脏肿瘤,占病例的85%,具有影响其发生和发展的复杂遗传途径。20%-50%的患者会发生RCC转移,通常累及远处器官。RCC的胃转移(GM)罕见,表现为黏膜下层的息肉样生长,占病例的0.2%-0.7%。本病例报告描述了一名84岁女性,患有福尔曼二级ccRCC,在根治性肾切除术后9年出现动脉粥样硬化性缺血性中风和胃肠道出血。胃镜检查发现一个12毫米的假性有蒂胃病变,伴有溃疡和出血,诊断为转移性ccRCC。讨论集中在RCC胃转移的罕见性、诊断挑战和预后因素。检测到消化转移后的中位生存期差异很大,其机制包括通过淋巴、经体腔或血行途径的直接侵犯和播散。预后标志物包括患者病史、症状、RCC诊断后的时间、整体健康状况和遗传因素。手术切除胃病变和靶向治疗是可以提高生存率的治疗选择。本病例报告强调需要进一步研究,以加强针对RCC病理生理学这一罕见方面的诊断和治疗策略。