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首页> 外文期刊>Medicine. >Late onset adrenal insufficiency after adrenalectomy due to latent nonclassical 21-hydroxylase deficiency: A case report
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Late onset adrenal insufficiency after adrenalectomy due to latent nonclassical 21-hydroxylase deficiency: A case report

机译:由于潜在的非生物化21-羟化酶缺乏,肾上腺切除后的晚期发病肾上腺功能不全:案例报告

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Rationale: Adrenal incidentaloma is sometimes complicated with 21-hydroxylase deficiency (21-OHD). Latent nonclassical 21-OHD in incidentaloma is difficult to diagnose. Although adrenalectomy in 21-OHD has been conducted when malignancy could not be excluded, adrenal insufficiency sometimes occurs, and it might not be observed immediately after operation. Here, we report a case of a 71-year-old man who experienced adrenal insufficiency over 2 decades postadrenalectomy, leading to a diagnosis of latent nonclassical 21-OHD. Patient concerns: A 71-year-old man was admitted to the hospital due to difficulty in movements and a sodium level of 119 mEq/L. His medical history revealed precocious puberty and left adrenalectomy because of an incidentaloma at 49 years of age, diagnosed pathologically as an adenoma. He did not attend follow-up visits because he did not have any symptoms. In 2017, 3 months before hospitalization, he experienced general fatigue. A few days before admittance, he complained of difficulty in moving and visual hallucination of small animals. Diagnoses: Laboratory evaluations revealed a high level of adrenocorticotropic hormone (ACTH) and low cortisol level. ACTH-stimulating test revealed a low basal level and low response for cortisol, and a high basal level and low response for 17-hydroxyprogesterone. We analyzed large gene deletion or conversion and the 9 most common micro mutations in the CYP21A2 gene by polymerase chain reaction; micro mutation of I172N and heterozygous large gene deletion or conversion were detected leading to the diagnosis of nonclassical 21-OHD. Interventions: Immediately, 100 mg hydrocortisone was administered, followed by daily hydrocortisone and saline. The symptoms and hyponatremia improved in a few days. He was discharged from the hospital on day 34 with a daily dose of 15 mg hydrocortisone. Lessons: Clinicians should be aware of late onset of adrenal insufficiency after adrenalectomy . In such cases, clinicians should not overlook the latent nonclassical 21-OHD.
机译:理由:肾上腺偶然瘤有时与21-羟化酶缺乏(21-OHD)复杂化。 Infinderaloma中的潜在非化学21-OHD难以诊断。虽然在21-OHD中的肾上腺切除术时已经进行了恶性肿瘤,但是有时会发生肾上腺功能不全,但操作后可能无法立即观察到。在这里,我们举报了一个71岁的男子,经历了210多年后期的肾上腺切除术,导致潜在的无菌21-OHD的诊断。患者担忧:由于运动困难和119 Meq / L的钠水平,一名71岁的男子被送往医院。他的病史揭示了早熟的青春期和左肾切除术,因为49岁的偶然瘤,作为腺瘤病理诊断。他没有参加后续访问,因为他没有任何症状。 2017年,住院前3个月,他经历了一般疲劳。入院前几天,他抱怨困难,在小动物的移动和视觉幻觉中。诊断:实验室评估显示出高水平的肾上腺皮质激素(ACTH)和低皮质醇水平。刺激性试验显示皮质醇的基础水平低,对17-羟丙基酮的高基础和低响应。我们通过聚合酶链反应分析了CYP21A2基因中的大型基因缺失或转化率和9个最常见的微突变;检测到I172N和杂合的大基因缺失或转化的微突变导致非分类21-OHD的诊断。干预:立即,施用100mg氢化胞蔻体,然后进行每日氢化胞蔻体和盐水。症状和低钠血症在几天内得到改善。他在第34天从医院出院,每日剂量为15毫克氢化鞘。课程:临床医生应该意识到肾上腺切除后肾上腺功能不全的后期发作。在这种情况下,临床医生不应该忽视潜在的非肤色21-OHD。

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