Arteriovenous Malformation in a Youth with Atypical Autism Symptoms.

Veena Sison, Tracy Stackhouse, Robert Breeze, Terry Hall, Pamela McKenzie, Nicole Tartaglia
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引用次数: 3

Abstract

Cerebral arteriovenous malformations (AVMs) present a challenge to diagnose in children with developmental disability, because of the overlap in behavioral symptoms and neurologic manifestations. They have been very rarely reported in conjunction with autism spectrum disorder. This case involves a 13 year old male with a history of autism spectrum disorder and significant behavioral issues diagnosed with a thalamic AVM following lateralizing neurologic symptoms. Despite radiosurgical treatment, hemorrhage followed consequently causing extensive neurologic injury and death. This case emphasizes the need for close follow up and coordination within a medical home for children with developmental disabilities. A multidisciplinary team approach is ideal to allow detection of subtle neurologic changes over time that may be masked as behavioral difficulties.

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非典型自闭症青少年动静脉畸形
脑动静脉畸形(AVMs)由于行为症状和神经系统表现的重叠,对发育性残疾儿童的诊断提出了挑战。它们很少与自闭症谱系障碍结合在一起。本病例涉及一名13岁男性,有自闭症谱系障碍病史和明显的行为问题,诊断为丘脑动静脉畸形,伴有侧化神经症状。尽管放射外科治疗,出血随后导致广泛的神经损伤和死亡。这一案例强调了在医疗院里对发育性残疾儿童进行密切跟进和协调的必要性。一个多学科团队的方法是理想的,允许检测细微的神经系统变化随着时间的推移,可能被掩盖为行为困难。
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