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。

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。
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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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