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单纯雄激素分泌性肾上腺肿瘤:临床特征与发病机制。

PURE ANDROGEN-PRODUCING ADRENAL TUMOR: CLINICAL FEATURES AND PATHOGENESIS.

出版信息

Endocr Pract. 2017 Apr 2;23(4):399-407. doi: 10.4158/EP161580.OR. Epub 2017 Jan 17.

Abstract

OBJECTIVE

Pure androgen-secreting adrenal tumors (PASATs) are extremely rare, most reports involving only a single case. This study examined 9 cases of PASAT, with an attempt to characterize its clinical features and to explore the pathogenesis.

METHODS

Clinical data of 9 patients with PASAT were retrospectively reviewed. Immunostaining was conducted, and the aryl hydrocarbon receptor-interacting protein gene (AIP) was amplified and directly sequenced.

RESULTS

The onset age of the patients ranged from 3.5 to 64 years. All 8 female patients had virilization, whereas the 7-year-old male patient presented with sexual precocity. Serum testosterone levels were elevated (4.1 to 52.3 nmol/L). Adrenal masses were detected and removed in all patients and histologically diagnosed as adrenocortical adenoma or carcinoma. Two patients had both PASATs and growth hormone (GH)-secreting pituitary adenomas (GH pituitary adenoma). Immunohistochemistry revealed nuclear immunoreactivity for p53 in 3 of 7 patients and nuclear immunoreactivity for cyclin D1 in 2 of 7 patients. Immunostaining of β-catenin showed nuclear, cytoplasmic, and membrane immunoreactivity (2 of 7 patients) or merely cytoplasmic immunoreactivity (1 of 7 patients). The adrenocortical carcinoma showed positive staining for both p53 and cyclin D1 and a high Ki-67 index of 60%. Mutations p.Lys177Argfs*19 and p.Asp287Val in the AIP gene were identified in PASATs of the 2 patients with concomitant presence of GH pituitary adenoma.

CONCLUSION

Clinical features of PASATs vary with gender and age of the patients. Abnormal p53 and β-catenin expression might be involved in the tumorigenesis of these tumors. AIP mutations might be responsible for the concomitant presence of PASATs and GH pituitary adenoma.

ABBREVIATIONS

ACA = adrenocortical adenoma ACC = adrenocortical carcinoma AIP = aryl hydrocarbon receptor-interacting protein DHEAS = dehydroepiandrosterone sulfate; GH growth hormone PASAT = pure androgen-secreting adrenal tumor.

摘要

目的

纯雄激素分泌性肾上腺肿瘤(PASAT)极为罕见,大多数报道仅涉及单个病例。本研究分析了 9 例 PASAT,旨在探讨其临床特征和发病机制。

方法

回顾性分析 9 例 PASAT 患者的临床资料。进行免疫组化染色,并扩增和直接测序芳香烃受体相互作用蛋白基因(AIP)。

结果

患者发病年龄 3.564 岁。8 例女性患者均表现为男性化,7 岁男性患者表现为性早熟。血清睾酮水平升高(4.152.3 nmol/L)。所有患者均检测到肾上腺肿块并切除,组织学诊断为肾上腺皮质腺瘤或癌。2 例患者同时患有 PASAT 和生长激素(GH)分泌性垂体腺瘤(GH 垂体腺瘤)。免疫组化显示 7 例患者中有 3 例 p53 核阳性,7 例患者中有 2 例 cyclin D1 核阳性。β-连环蛋白免疫组化显示 7 例患者中有 2 例核、细胞质和膜阳性(7 例患者中有 2 例)或仅细胞质阳性(7 例患者中有 1 例)。肾上腺皮质癌同时表达 p53 和 cyclin D1,Ki-67 指数为 60%。同时伴有 GH 垂体腺瘤的 2 例 PASAT 患者的 AIP 基因中检测到 p.Lys177Argfs*19 和 p.Asp287Val 突变。

结论

PASAT 的临床特征因患者性别和年龄而异。异常的 p53 和 β-连环蛋白表达可能参与了这些肿瘤的发生。AIP 突变可能是 PASAT 与 GH 垂体腺瘤同时存在的原因。

缩写

ACA = 肾上腺皮质腺瘤;ACC = 肾上腺皮质癌;AIP = 芳香烃受体相互作用蛋白;DHEAS = 脱氢表雄酮硫酸盐;GH = 生长激素;PASAT = 纯雄激素分泌性肾上腺肿瘤。

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