University of Health Sciences Turkey, İstanbul Zeynep Kamil Women and Children Diseases Hospital, Clinic of Pediatric Endocrinology, İstanbul, Turkey
J Clin Res Pediatr Endocrinol. 2020 Nov 25;12(4):383-392. doi: 10.4274/jcrpe.galenos.2020.2019.0220. Epub 2020 May 20.
Potent glucocorticoids (GC) cause iatrogenic Cushing’s syndrome (ICS) due to suppression of hypothalamo-pituitary-adrenal (HPA) axis and may progress to adrenal insufficiency (AI). The aim was to review the clinical and laboratory findings of patients with ICS and to investigate other serious side effects.
The possibility of AI was investigated by low-dose adrenocorticotrophic hormone test. Hydrocortisone was started in patients with adrenal failure.
Fourteen patients (five boys) with ages ranging from 0.19 to 11.89 years were included. The duration of GC exposure ranged from 1 to 72 months. Ten patients were prescribed topical GC and the rest had oral exposure. Moon face and abdominal obesity were detected in all patients. At presentation, 12 of 14 had AI and two infants had hypercalcemia and nephrocalcinosis. Of 11 patients, ultrasonography revealed hepatosteatosis in five. A cream for diaper dermatitis was used in one infant and the active ingredient was listed as panthenol. However, blood and urine steroid analyses revealed that all endogenous steroids were suppressed. Median (range) time to normalization of HPA axis function was 60 (30-780) days.
The majority (85%) of patients had life-threatening AI and two patients had hypercalcemia. These results highlight the serious side-effects of inappropriate use of potent GCs, especially in infants. The recovery of the HPA axis in children might take as long as three years. Parents should be informed regarding the possibility of some products containing unlisted synthetic GC and to be aware of their side effects.
强效糖皮质激素(GC)通过抑制下丘脑-垂体-肾上腺(HPA)轴引起医源性库欣综合征(ICS),并可能进展为肾上腺功能不全(AI)。目的是回顾 ICS 患者的临床和实验室发现,并探讨其他严重的副作用。
通过小剂量促肾上腺皮质激素试验调查 AI 的可能性。对肾上腺功能衰竭的患者开始使用氢化可的松。
共纳入 14 名(5 名男性)年龄在 0.19 至 11.89 岁的患者。GC 暴露时间从 1 至 72 个月不等。10 名患者使用局部 GC,其余患者则使用口服 GC。所有患者均出现满月脸和腹部肥胖。就诊时,14 名患者中有 12 名患有 AI,2 名婴儿患有高钙血症和肾钙质沉着症。11 名患者中有 5 名超声显示肝脂肪变性。一名患有尿布皮炎的婴儿使用了一种乳膏,其有效成分列为泛醇。然而,血液和尿液类固醇分析显示所有内源性类固醇均被抑制。HPA 轴功能正常化的中位数(范围)时间为 60(30-780)天。
大多数(85%)患者存在危及生命的 AI,有 2 名患者出现高钙血症。这些结果突出了不适当使用强效 GC 的严重副作用,尤其是在婴儿中。儿童 HPA 轴的恢复可能需要长达 3 年的时间。应告知家长注意某些产品可能含有未列出的合成 GC 及其副作用。