Idiopathic spinal epidural hematoma in an infant: A case report with peculiar manifestation

IF 0.6
K. Alghamdi, Ibrahim Omer, Abdelrahman Al Arjani
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引用次数: 0

Abstract

Idiopathic spinal epidural hematoma (SEH) might be an extremely rare cause of spine compression. It is most common between the fourth and fifth decades of life. It is sporadic in children and is often complicated due to the limitations of a neurologic examination and nonspecific symptoms within the pediatric population. It is typically an isolated event. Only a few cases of relapsing paraparesis due to idiopathic SEH have been mentioned in the literature in adults. We are presenting a rare case of idiopathic SEH in a 1-year-old girl whose diagnosis was deferred after a recent similar history of paraparesis occurred after her scheduled immunization and went on for around 2 weeks, after which the patient recovered completely. However, 2 months later, the patient presented again with paraparesis, and the magnetic resonance imaging revealed an idiopathic SEH. We are detailing this case to raise the plausibility of a remission and relapse phenomenon within the idiopathic SEH presentation that may mimic some neurological disorders of infancy and childhood. The present case was managed surgically and yielded full recovery.
特发性脊髓硬膜外血肿(SEH)可能是一个极其罕见的原因脊柱压迫。最常见的是在40岁到50岁之间。它在儿童中是散发的,由于神经学检查的局限性和儿科人群的非特异性症状,通常是复杂的。这是典型的孤立事件。文献中只有少数成人因特发性SEH而复发性麻痹的病例被提及。我们报告一例罕见的特发性SEH病例,一名1岁的女孩,在她预定的免疫接种后出现了类似的麻痹史,并持续了大约2周,之后患者完全康复,因此推迟了诊断。然而,2个月后,患者再次出现麻痹,磁共振成像显示特发性SEH。我们详细介绍了这个病例,以提高特发性SEH表现中缓解和复发现象的合理性,这可能模仿了一些婴儿期和儿童期的神经系统疾病。本病例经手术治疗并完全恢复。
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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CiteScore
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