首页> 美国卫生研究院文献>Acta Endocrinologica (Bucharest) >PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE (PPNAD) PRESENTING AS CUSHING SYNDROME IN A CHILD AND REVIEW OF LITERATURE
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PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE (PPNAD) PRESENTING AS CUSHING SYNDROME IN A CHILD AND REVIEW OF LITERATURE

机译:初级着色的结节性肾上腺皮质疾病(PPNAD)作为儿童缓冲综合征文学评论

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摘要

Cushing syndrome in the paediatric age group is very difficult to diagnose due to atypical presenting features in children. Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing syndrome in children and it has characteristic gross and microscopic pathologic features. We report a case of PPNAD in a 16-year-old boy who was evaluated in our hospital with chief complaints of poor height velocity and rapid weight gain for 2-3 years before presentation. Proper evaluation showed ACTH-independent Cushing syndrome with normal imaging. Total bilateral adrenalectomy was performed followed by hormones replacement. 6 months after surgery, significant acceleration of height velocity was noticed. Patient also lost body weight and developed secondary sexual characteristics.
机译:由于儿童的非典型呈现特征,儿科年龄组中的缓冲综合征非常难以诊断。原发性着色的结节性肾上腺皮质疾病(PPNAD)是儿童独立于独立的缓冲综合征的罕见原因,具有特征性的毛细管和显微病理特征。我们举报了一个16岁男孩的PPNAD案例,在我们的医院评估了高度速度差,在介绍前2 - 3年的速度较差和重量迅速增长。适当的评估显示与正常成像的独立独立的缓冲综合征。进行两侧肾上腺切除术,然后进行荷尔蒙替代。手术后6个月,注意到高度速度的显着加速度。患者也失去了体重并发展了次要性特征。

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