Atypical carcinoid of the primary kidney with retroperitoneal metastasis 15 years later: A case report and literature review

IF 0.5 Q4 UROLOGY & NEPHROLOGY Urology Case Reports Pub Date : 2024-11-21 DOI:10.1016/j.eucr.2024.102893
Qiang Wang, Dong Zhuo, Houbao Huang, Jianping Tao
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引用次数: 0

Abstract

Primary renal neuroendocrine tumors (NETs) are extremely rare among renal malignancies. According to pathological manifestations, carcinoid can be divided into four types: typical carcinoid, atypical carcinoid, large cell and small cell neuroendocrine carcinoma. Primary or secondary retroperitoneal carcinoid is even rarer than renal carcinoid. This article reports a patient with renal carcinoid complicated with retroperitoneal metastasis, who developed retroperitoneal metastasis 15 years after radical nephrectomy. Through the analysis of this case and the combination of the existing published literature, it is aimed to provide valuable references for clinicians in treating patients with renal carcinoid or with metastasis.
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原发性肾脏非典型类癌,15 年后腹膜后转移:病例报告和文献综述
原发性肾神经内分泌肿瘤(NET)在肾脏恶性肿瘤中极为罕见。类癌根据病理表现可分为四种类型:典型类癌、非典型类癌、大细胞和小细胞神经内分泌癌。原发性或继发性腹膜后类癌比肾脏类癌更为罕见。本文报告了一名肾脏类癌并发腹膜后转移的患者,该患者在根治性肾切除术后15年出现腹膜后转移。通过对该病例的分析,并结合现有已发表的文献,旨在为临床医生治疗类肾癌或转移瘤患者提供有价值的参考。
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
期刊最新文献
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