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The Diagnosis and Treatment of Virilizing and Feminizing Adrenal Syndrome

机译:阳and女性化肾上腺综合征的诊治

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Objective: To inquire into diagnosis, and treatment of virilizing and feminizing a-drenal syndrome, differential diagnosis between benign and malignant sex hormone producing adrenal neo-plasma and, treatment principles of congenital adrenal hyperplasia (CAH). Methods: Eight cases of CAH and 5 cases of sex hormone producing adrenal neoplasma were admitted to hospital during 1986-1996. The former included 3 rare cases of 17 a hydroxylase deficiency. The latter included 3 cases of feminizing adrenal tumor and 2 cases of virilizing adrenal tumor. Results: Weight, size and CT of the tumor, DHEA, 17 -ks, sex hormone levels, infiltration, and metastasis were closely related to the degree of differentiation of the tumors. Conclusion: Virilizing and feminizing adrenal neoplasm were removed surgically by different incisions. Modified subcostal incision was recommended as the best choice for huge adrenal mass. Corticoadrenal hormone treatment fa CAH should be individualized according to the different types of the disease. Sex hormones were not suitable for children suffering from 17 hydroxylase deficiency before puberty.
机译:目的:探讨男性化和女性化的α-肾上腺综合征的诊断和治疗,产生良性和恶性性激素的肾上腺肿瘤的鉴别诊断,以及先天性肾上腺增生(CAH)的治疗原则。方法:1986-1996年收治8例CAH和5例产生性激素的肾上腺肿瘤。前者包括3种罕见的17种羟化酶缺乏症。后者包括3例女性化的肾上腺肿瘤和2例男性化的肾上腺肿瘤。结果:肿瘤的重量,大小和CT,DHEA,17-ks,性激素水平,浸润和转移与肿瘤的分化程度密切相关。结论:用不同的切口通过手术切除了已使女性化和女性化的肾上腺肿瘤。改良的肋下切口被推荐为巨大肾上腺肿块的最佳选择。 CAH的肾上腺皮质激素治疗应根据疾病的不同类型进行个体化。性激素不适用于青春期前患有17种羟化酶缺乏症的儿童。

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