嗜铬细胞瘤合并腹膜后转移1例
Pheochromocytoma with Retroperitoneal Metastasis: A Case Report
DOI: 10.12677/ACM.2021.115322, PDF,   
作者: 崔建新：青岛大学，山东 青岛；浙江省人民医院，浙江 杭州；缪 嘉, 张大宏：浙江省人民医院，浙江 杭州；庞晓飞, 冯 阳：青岛大学，山东 青岛
关键词: 嗜铬细胞瘤；腹膜后转移；神经内分泌肿瘤；Pheochromocytoma； Retroperitoneal Metastasis； Neuroendocrine Tumors
摘要: 嗜铬细胞瘤和副神经节瘤是一种罕见的神经内分泌肿瘤，其来源于肾上腺髓质或肾上腺外副神经节的嗜铬细胞。其具体的发病机制、转移方式及临床转归尚不明确，国内外相关报道较少。现对我院1例嗜铬细胞瘤伴腹膜后转移患者进行临床分析及随访，报道如下。
Abstract: Pheochromocytoma and paraganglioma are rare neuroendocrine tumors that are derived from pheochromophore cells in the adrenal medulla or extra-adrenal paraganglia. Its specific pathogenesis, metastasis and clinical outcome are still unclear, and there are few relevant reports at home and abroad. A case of pheochromocytoma with retroperitoneal metastasis in our hospital is now undergoing clinical analysis and follow-up. The report is as follows.
文章引用：崔建新, 缪嘉, 庞晓飞, 冯阳, 张大宏. 嗜铬细胞瘤合并腹膜后转移1例[J]. 临床医学进展, 2021, 11(5): 2239-2243. https://doi.org/10.12677/ACM.2021.115322

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