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The prevalence of testicular adrenal rest tumors and associated factors in postpubertal patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency

机译:21-羟化酶缺乏症致青春期后发性先天性肾上腺皮质增生患者睾丸肾上腺休息肿瘤的发生率及相关因素

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摘要

Development of a testicular adrenal rest tumor (TART) is common in males with congenital adrenal hyperplasia, and it can be an important cause of infertility. In the present study, we observed the prevalence of TARTs, and analyzed its associated factors in patients with 21 -hydroxylase deficiency. Testicular ultrasonography was performed in 48 postpubertal male patients aged 10.6 to 27.1 years. To determine whether patients were undertreated, we analyzed the serum 17-hydroxyprogesterone (17-OHP) levels to the time of ultrasonographic measurement and calculated the percentage of measurements when serum 17-OHP level was >10 ng/mL relative to the total number of measurements during the follow-up period. We divided the 6-year period before ultrasonographic measurement (time 0) into three 2-year intervals and calculated the average concentration of serum 17-OHP in each interval to give a -2nd to 0 year-average concentration (-2-0YAC), -4-2 YAC and -6-4YAC. A TART was detected by ultrasonography in 31 of 48 patients (64.6%) and the median maximal cross-sectional area of the TARTs was 0.71 (0.03, 4.95) cm2. The corrected final adult height was lower, and -4-2YAC and body mass index were higher in patients with TART than in those without. After controlling for the type of 21-hydroxylase deficiency, hydrocortisone-equivalent dose, age, and -6-4YAC, the size of TART was associated with a high undertreatment percentage with a marginal statistical significance. These results suggest that strict disease control is mandatory and regular examination with testicular ultrasonography is recommended in male patients, regardless of the type of 21-hydroxylase deficiency.
机译:先天性肾上腺增生的男性中睾丸肾上腺休息肿瘤(TART)的发展很普遍,它可能是不孕的重要原因。在本研究中,我们观察了21羟化酶缺乏症患者中TART的患病率,并分析了其相关因素。在48位年龄在10.6至27.1岁之间的男性青春期患者中进行了睾丸超声检查。为了确定患者是否治疗不足,我们分析了超声检查时的血清17-羟孕酮(17-OHP)水平,并计算了当血清17-OHP水平> 10 ng / mL时相对于总血清数的测量百分比在随访期间进行测量。我们将超声检查前的6年时间段(时间0)分为两个2年间隔,并计算每个间隔中血清17-OHP的平均浓度,得出-2至0年平均浓度(-2-0YAC) ,-4-2 YAC和-6-4YAC。通过超声检查在48例患者中有31例(64.6%)检测到TART,并且TART的最大横截面积中位数为0.71(0.03,4.95)cm2。 TART患者的校正后最终成人身高较低,-4-2YAC和体重指数较高。在控制了21-羟化酶缺乏症的类型,氢化可的松当量的剂量,年龄和-6-4YAC之后,TART的大小与治疗不足率高相关,具有统计学意义。这些结果表明,无论21-羟化酶缺乏症的类型如何,男性患者均应严格控制疾病,并建议定期进行睾丸超声检查。

著录项

  • 来源
    《Endocrine journal》 |2011年第6期|p.501-508|共8页
  • 作者单位

    Department of Pediatrics, Seoul National University College of Medicine, Seoul, 110-769, Korea;

    Department of Pediatrics, Inje University Ilsan Paik Hospital, Goyang, 411-706, Korea;

    Department of Pediatrics, Inje University Pusan Paik Hospital, Pusan, 614-735, Korea;

    Department of Pediatrics, Seoul National University College of Medicine, Seoul, 110-769, Korea;

    Department of Pediatrics, Seoul National University College of Medicine, Seoul, 110-769, Korea;

    Department of Pediatrics, Seoul National University College of Medicine, Seoul, 110-769, Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    testicular adrenal rest tumor; congenital adrenal hyperplasia;

    机译:睾丸肾上腺休息肿瘤;先天性肾上腺增生;
  • 入库时间 2022-08-18 01:33:12

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