Dyke Davidoff Masson: A Case Report.

IF 1.4 Q3 PEDIATRICS
Global Pediatric Health Pub Date : 2024-03-03 eCollection Date: 2024-01-01 DOI:10.1177/2333794X241234733
Boumeriem Khaoula, Bourekba Iliass, Allali Nazik, Chat Latifa, El Haddad Siham
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引用次数: 0

Abstract

Dyke Davidoff-Masson syndrome is a rare neurological condition that results from brain injury during early childhood stages. The precise incidence of this condition is unknown, with a slight male predominance, and adult forms have been documented. Imaging findings reveal hemisphere atrophy along with ipsilateral compensatory skull changes and hyper-pneumatization of mastoid cells. The treatment approach involves anti-epileptic medications and hemispherectomy is reserved for cases with intractable seizures. This case report delineates the clinical manifestation and therapeutic approach employed in an 8-year-old male patient exhibiting pharmaco-resistant left hemi-body convulsive seizures. The magnetic resonance imaging (MRI) findings revealed right cerebral hemiatrophy, mesencephalon atrophy, ipsilateral calvarial hypertrophy and hyperpneumatization of mastoid cells. The objective of this study is to contribute to the existing literature by presenting this rare case report. We propose that in cases involving pediatric pharmaco-resistant epilepsy, it is essential to conduct further investigations to establish a comprehensive management strategy.

戴克-大卫杜夫-马森:病例报告
戴克-戴维杜夫-马森综合征是一种罕见的神经系统疾病,由幼年时期的脑损伤引起。该病的确切发病率尚不清楚,男性略占优势,也有成人病例的记录。影像学检查结果显示大脑半球萎缩,同侧颅骨代偿性改变,乳突细胞过度气化。治疗方法包括服用抗癫痫药物,半球切除术只用于难治性癫痫发作的病例。本病例报告描述了一名 8 岁男性患者的临床表现和治疗方法,该患者表现为药物抵抗性左侧半身抽搐性癫痫发作。磁共振成像(MRI)结果显示患者右侧大脑半萎缩、间脑萎缩、同侧小脑肥大和乳突细胞过度充气。本研究旨在通过介绍这一罕见病例报告,为现有文献做出贡献。我们建议,在涉及小儿药物耐药性癫痫的病例中,必须进行进一步的检查,以制定全面的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Global Pediatric Health
Global Pediatric Health Nursing-Pediatrics
CiteScore
2.20
自引率
0.00%
发文量
105
审稿时长
12 weeks
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