先天性皮质过度增生症:婴儿哭闹不止的罕见原因。临床病例报告。

IF 0.7 4区 医学 Q4 PEDIATRICS
Archivos argentinos de pediatria Pub Date : 2024-08-01 Epub Date: 2024-01-04 DOI:10.5546/aap.2023-10220.eng
Ana Braslavsky, María E López
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引用次数: 0

摘要

我们在此描述一个病例,一名两个月大的婴儿因过度哭闹多次就诊,最初被解释为胃肠道原因。由于症状持续存在,在活动四肢时触及右胫骨前侧肿块,因此怀疑是骨折。X光片显示长骨的骨骺多骨质受累和皮质受累病变。卡菲-德托尼-希尔弗曼综合征被确诊,并开始使用非甾体类抗炎药物进行治疗,结果症状得到缓解。随后,通过鉴定致病杂合变体 COL1A1,确诊了该病。这是一种罕见病,估计发病率为 48/100000,迄今为止描述的病例不到 150 例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital cortical hyperostosis: a rare cause of inconsolable crying in a baby. Clinical case report.

Here we describe the case of a 2-month-old infant who consulted several times due to excessive crying, initially interpreted as having a gastrointestinal cause. Since the symptom persisted, a fracture was suspected due to its association with mobilization of the limbs and palpation of a mass on the anterior aspect of the right tibia. X-rays showed diaphyseal polyostotic involvement and lesions compatible with cortical involvement of long bones. Caffey-De Toni-Silverman syndrome was diagnosed and treatment with nonsteroidal anti-inflammatory drugs was initiated, resulting in symptom remission. Subsequently, the diagnosis was confirmed by the identification of the pathogenic heterozygous variant COL1A1. This is a rare condition with an estimated incidence of 48/100 000 individuals, and less than 150 cases have been described to date.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
286
审稿时长
6-12 weeks
期刊介绍: Archivos Argentinos de Pediatría is the official publication of the Sociedad Argentina de Pediatría (SAP) and has been published without interruption since 1930. Its publication is bimonthly. Archivos Argentinos de Pediatría publishes articles related to perinatal, child and adolescent health and other relevant disciplines for the medical profession.
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