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机构地区:[1]中南大学湘雅二医院泌尿外科,长沙410011
出 处:《中南大学学报(医学版)》2012年第6期633-636,共4页Journal of Central South University :Medical Science
摘 要:为探讨肾上腺皮质嗜酸细胞腺瘤的诊断和治疗。本研究回顾性分析3例肾上腺皮质嗜酸细胞腺瘤的临床资料并复习相关文献。3例患者中1例表现为女性男性化,其余2例无特异表现。肿瘤包膜完整,呈非浸润性生长。光镜下,肿瘤细胞胞质丰富,嗜酸性,未见明显核分裂相和坏死。术后严格随访,3例均未见肿瘤复发和转移。肾上腺皮质嗜酸细胞腺瘤非常罕见,且大多数为良性,术前难以明确诊断,治疗首选手术切除,术后应严格随访。To investigate the diagnosis and surgical treatment of adrenocortical oncocytoma. The clinical data from three cases of adrenocortical oncocytomas (ACOs) were retrospectively analyzed and discussed in light of the relevant literature. In these three cases, one presented with virilization, while the other two cases had no typical clinical features. The tumor was completely encapsulated and was non-invasive. Microscopicall)5 the tumor cells showed neither mitosis nor necrosis, with abundant eosinophilic cytoplasm. No recurrence or metastasis was discovered after close follow-up observation for 12-24 months. Adrenocortical ACOs are rather rare, and most of them are benign. It was hard to make a confirmed diagnosis of ACOs before surgery. Resection of tumor is the best choice, and dose follow-up observation is essential.
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