Gannagé-Yared M H, Slaba S, Rizk T, Chidiac Wehbe R-M
Department of Endocrinology, Saint- Joseph University, Beirut, Lebanon.
J Endocrinol Invest. 2007 May;30(5):434-8. doi: 10.1007/BF03346323.
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.
库欣综合征(CS)在儿童中较为罕见。关于CS患儿双侧岩下窦采血(BIPSS)的信息有限。在该检查过程中,总是使用促肾上腺皮质激素释放激素(CRH)来刺激促肾上腺皮质激素(ACTH)值。此外,生长发育迟缓是小儿CS的主要并发症,主要是由于生长激素(GH)受到严重抑制,且在疾病治愈后仍持续数月。CS治愈后早期使用重组生长激素治疗可能会部分逆转这一现象。我们在此报告一例7岁患库欣病(CD)的儿童,伴有严重生长发育迟缓。磁共振成像未显示垂体腺瘤,使用去氨加压素进行的BIPSS显示存在中央到外周(C/P)梯度;然而,经蝶窦手术(TSS)未能治愈该病,因此需要进行双侧肾上腺切除术。疾病治愈后,在未进行任何生长激素治疗的情况下,生长发育迟缓出现了部分追赶。我们的病例进一步证明,BIPSS可以在非常年幼的CD患儿中安全进行。它还首次表明,在检查过程中使用去氨加压素与使用CRH能提供相同的信息,同时也证实了TSS在非常年幼的儿童中成功率较低这一事实。最后,这表明CS患儿的生长发育迟缓在手术治愈疾病后无需任何生长激素治疗即可部分逆转,并且在皮质类固醇替代治疗期间观察到的高胰岛素样生长因子-I(IGF-I)是由于IGF-I抵抗状态所致。