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一名患有 TSC2/PKD1 连续基因缺失综合征的儿童,经托伐普坦治疗后迅速增大的肾囊肿得到成功缓解。

A child with TSC2/PKD1 contiguous gene deletion syndrome successfully treated with tolvaptan for rapidly enlarging renal cysts.

机构信息

Division of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, 36-1 Nishi-cho, Yonago, Tottori, 683-8504, Japan.

Division of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, 36-1 Nishi-cho, Yonago, Tottori, 683-8504, Japan. hirokiy1+

出版信息

CEN Case Rep. 2024 Oct;13(5):351-355. doi: 10.1007/s13730-024-00854-6. Epub 2024 Feb 27.

DOI:10.1007/s13730-024-00854-6
PMID:38411894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11442821/
Abstract

Tolvaptan, a vasopressin receptor antagonist, has been shown to be effective in the treatment of renal cysts in ADPKD. However, tolvaptan is not indicated for pediatric patients, and reports of its use are rare, making its efficacy and adverse reactions unclear. Herein, we present the case of an 11-year-old girl who had vitiligo from birth. She was diagnosed with West syndrome at 6 months of age and tuberous sclerosis at 2 years of age. At the age of 6 years, an abdominal magnetic resonance imaging (MRI) revealed multiple bilateral renal cysts, and she was diagnosed with ADPKD. Abdominal MRI scans performed at 10 years and 11 years showed rapid renal cyst enlargement, and the renal prognosis was judged to be poor. The patient was treated with tolvaptan to delay cyst exacerbation. There were no apparent adverse events after the initiation of treatment, and the MRI performed 12 months after treatment initiation showed that renal cyst enlargement was suppressed. The results suggest that tolvaptan may be effective in pediatric patients with severe ADPKD who have rapidly enlarging renal cysts, although evaluation of renal cyst enlargement and side effects should be continued.

摘要

托伐普坦是一种血管加压素受体拮抗剂,已被证明可有效治疗 ADPKD 中的肾囊肿。然而,托伐普坦不适用于儿科患者,且其使用的报告罕见,因此其疗效和不良反应尚不清楚。在此,我们报告了一例 11 岁女孩的病例,她出生时就患有白癜风。她在 6 个月大时被诊断为 West 综合征,2 岁时被诊断为结节性硬化症。6 岁时,腹部磁共振成像(MRI)显示双侧多发性肾囊肿,被诊断为 ADPKD。10 岁和 11 岁时进行的腹部 MRI 扫描显示肾囊肿迅速增大,判断肾脏预后不良。该患者开始接受托伐普坦治疗以延缓囊肿恶化。治疗开始后没有明显的不良反应,治疗开始 12 个月后的 MRI 显示肾囊肿增大得到抑制。结果表明,托伐普坦可能对快速增大肾囊肿的严重 ADPKD 儿科患者有效,尽管应继续评估肾囊肿的增大和副作用。

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本文引用的文献

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Effects of Hydrochlorothiazide and Metformin on Aquaresis and Nephroprotection by a Vasopressin V2 Receptor Antagonist in ADPKD: A Randomized Crossover Trial.血管加压素 V2 受体拮抗剂治疗多囊肾病时氢氯噻嗪和二甲双胍对水通透性和肾脏保护作用的随机交叉试验。
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International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people.国际共识声明:儿童和青少年常染色体显性遗传性多囊肾病的诊断和管理。
Nat Rev Nephrol. 2019 Nov;15(11):713-726. doi: 10.1038/s41581-019-0155-2.
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Tolvaptan use in children and adolescents with autosomal dominant polycystic kidney disease: rationale and design of a two-part, randomized, double-blind, placebo-controlled trial.托伐普坦在常染色体显性遗传多囊肾病患儿和青少年中的应用:一项两部分、随机、双盲、安慰剂对照试验的原理和设计。
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