首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Use of desmopressin as an alternative to corticotropin-releasing hormone during inferior petrosal sinus sampling in a child with Cushing's disease.
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Use of desmopressin as an alternative to corticotropin-releasing hormone during inferior petrosal sinus sampling in a child with Cushing's disease.

机译:在库欣病患儿岩下窦取样期间使用去氨加压素作为促肾上腺皮质激素释放激素的替代药物。

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摘要

Cushing's syndrome (CS) is rare in children. Information on bilateral inferior petrosal sinus sampling (BIPSS) in children with CS is limited. In the procedure CRH is always used to stimulate ACTH values. In addition, growth failure is the main complication of pediatric CS, mainly due to a profound GH suppression that persists for a few months after cure of the disease. Early treatment with recombinant GH after CS cure may partly reverse this phenomenon. We report herein a case of Cushing's disease (CD) in a 7-yr-old child, presenting with severe growth failure. No pituitary adenoma was shown on magnetic resonance imaging and a BIPSS using desmopressin allowed the identification of a central to peripheral (C/P) gradient; however transphenoidal surgery (TSS) did not cure the disease thus requiring the performance of bilateral adrenalectomy. After cure of the disease, a partial catch up of the growth delay occurred without any GH treatment. Our case reinforces the fact that BIPSS can be performed safely in very young children with CD. It also suggests for the first time that the use of desmopressin during the procedure gives the same information as CRH, as well as confirming the fact that the success of TSS is poor in very young children. Finally, it suggests that growth failure in children with CS can be partially reversed after surgical cure of the disease without any GH treatment and that the high IGF-I observed during corticosteroid replacement therapy is due to a state of IGF-I resistance.
机译:库欣综合征 (CS) 在儿童中很少见。CS 患儿双侧岩下窦取样 (BIPSS) 的信息有限。在此过程中,CRH始终用于刺激ACTH值。此外,生长迟缓是小儿CS的主要并发症,主要是由于严重的生长激素抑制,在疾病治愈后持续数月。CS 治愈后早期使用重组 GH 治疗可能会部分逆转这种现象。我们在此报告了一例 7 岁儿童的库欣病 (CD) 病例,表现为严重的生长障碍。磁共振成像未显示垂体腺瘤,使用去氨加压素的 BIPSS 可识别中央至外周 (C/P) 梯度;然而,经蝶骨手术 (TSS) 不能治愈该疾病,因此需要进行双侧肾上腺切除术。疾病治愈后,在没有任何生长激素治疗的情况下发生了生长迟缓的部分赶上。我们的案例强化了这样一个事实,即 BIPSS 可以安全地用于患有 CD 的非常年幼的儿童。它还首次表明,在手术过程中使用去氨加压素可提供与CRH相同的信息,并证实了TSS在非常年幼的儿童中成功率低的事实。最后,它表明,CS患儿的生长迟缓可以在没有任何GH治疗的情况下手术治愈后部分逆转,并且在皮质类固醇替代治疗期间观察到的高IGF-I是由于IGF-I抵抗状态。

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