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小儿非热性惊厥:要点谨记

Nonfebrile Seizures in Pediatrics: Key Points to Remember.

作者信息

Anjos Mariana M, Figueireido Ana M, Cardoso Patricia, Costa Filipa, Morais Julieta

机构信息

Pediatrics, Centro Hospitalar do Médio Tejo, Torres Novas, PRT.

出版信息

Cureus. 2024 Jan 30;16(1):e53233. doi: 10.7759/cureus.53233. eCollection 2024 Jan.

DOI:10.7759/cureus.53233
PMID:38425628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10902737/
Abstract

Seizures are the most common neurological disorder in pediatrics, and their initial approach aims at clinical stabilization. A thorough patient evaluation may provide important clues for the etiological diagnosis. A 12-month-old female child was observed in the emergency department after experiencing her first apyretic seizure. She had a history of congenital alopecia and, on physical examination, presented subtotal alopecia and milia. Initial investigation revealed hypocalcemia; therefore, intravenous calcium correction was started with a partial response. The analytical study was extended, revealing hypophosphatemia, elevated parathormone, and 1,25(OH) vitamin D with normal 25(OH) vitamin D. The genetic analysis confirmed hereditary vitamin D-resistant rickets (HVDRR). The integration of the findings was crucial to diagnostic reasoning and to guide further investigation. HVDRR is a rare disorder, with more severe clinical presentations associated with alopecia. Early diagnosis and treatment are fundamental to minimize the impact on growth and the development of other comorbidities.

摘要

癫痫发作是儿科最常见的神经系统疾病,其初始治疗旨在实现临床稳定。全面的患者评估可为病因诊断提供重要线索。一名12个月大的女童在经历首次无热惊厥后被送往急诊科。她有先天性脱发病史,体格检查发现部分脱发和粟丘疹。初步检查发现低钙血症;因此开始静脉补钙治疗,但仅有部分反应。进一步的分析研究发现低磷血症、甲状旁腺激素升高、1,25(OH)维生素D升高而25(OH)维生素D正常。基因分析确诊为遗传性维生素D抵抗性佝偻病(HVDRR)。综合各项检查结果对于诊断推理及指导进一步检查至关重要。HVDRR是一种罕见疾病,临床表现更为严重,常伴有脱发。早期诊断和治疗对于将其对生长及其他合并症发展的影响降至最低至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/678e67e65c21/cureus-0016-00000053233-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/e590d4997b32/cureus-0016-00000053233-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/8ec295b31497/cureus-0016-00000053233-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/92ab67a5b4d2/cureus-0016-00000053233-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/678e67e65c21/cureus-0016-00000053233-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/e590d4997b32/cureus-0016-00000053233-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/8ec295b31497/cureus-0016-00000053233-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/92ab67a5b4d2/cureus-0016-00000053233-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/10902737/678e67e65c21/cureus-0016-00000053233-i04.jpg

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本文引用的文献

1
Acute Seizures-Work-Up and Management in Children.儿童急性发作的评估和处理。
Semin Neurol. 2020 Dec;40(6):606-616. doi: 10.1055/s-0040-1718718. Epub 2020 Nov 5.
2
Cinacalcet treatment experience in hereditary vitamin D resistant rickets.西那卡塞治疗遗传性维生素D抵抗性佝偻病的经验
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Eight-year-old Boy with New-onset Seizure.八岁新发癫痫男孩。
Clin Pract Cases Emerg Med. 2019 Apr 12;3(2):89-94. doi: 10.5811/cpcem.2019.4.42547. eCollection 2019 May.
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Familial Vitamin D-dependent rickets Type 2A: A report of two cases with alopecia and oral manifestations.家族性2A型维生素D依赖性佝偻病:两例伴有脱发和口腔表现的病例报告。
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Rare, genetically conditioned forms of rickets: Differential diagnosis and advances in diagnostics and treatment.罕见的遗传性佝偻病形式:鉴别诊断及诊断和治疗的进展。
Clin Genet. 2018 Jul;94(1):103-114. doi: 10.1111/cge.13229. Epub 2018 Mar 25.
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Genetic Causes of Rickets.佝偻病的遗传病因。
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Rickets.佝偻病。
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The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets.西那卡塞作为遗传性1,25-二羟维生素D3抵抗性佝偻病辅助治疗的有效性
J Clin Res Pediatr Endocrinol. 2017 Jun 1;9(2):172-178. doi: 10.4274/jcrpe.3486. Epub 2016 Oct 31.
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Acute Symptomatic Seizures Caused by Electrolyte Disturbances.电解质紊乱引起的急性症状性癫痫发作
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