小儿Chiari II型畸形、腰骶部脊膜膨出、软骨发育不全和呼吸调节功能受损的康复一例报告及文献复习。

IF 0.8 Q4 PEDIATRICS
Riekje Neißkenwirth, Christian Mathys, Marc-Phillip Hitz, Tobias Linden, Martin Groß
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引用次数: 0

摘要

chiari II型畸形发生率为千分之一,可导致后窝畸形。在Chiari II型畸形中,几乎总是存在腰骶脊膜膨出。软骨发育不全是侏儒症最常见的原因,每26000个活产儿中就有一个发生。Chiari II型畸形和软骨发育不全均可引起颅颈交界处压迫和连续的脑积水。病例介绍:我们报告了一名三岁的男性,患有Chiari II型畸形、腰骶部脊膜膨出和软骨发育不全。据作者所知,这是迄今为止报告的第二例此类病例。在出生后的第一个月进行了腰骶脊膜膨出的手术治疗和脑室-腹膜分流术的植入。两岁时,枕寰枢椎狭窄需要脊柱减压和椎板切除术。该患儿就诊于门诊,表现为危及生命的呼吸失调,包括长时间呼气性呼吸暂停伴紫绀(PEAC)、获得性中枢性低通气综合征、中枢性睡眠呼吸暂停和阻塞性睡眠呼吸暂停。他还表现出语言发育迟缓、截瘫、神经性膀胱和侏儒症。患者接受无创通气,并有一套单独适应的辅助和治疗装置。咳嗽功能不全需要采用机械充气-呼气法。定期进行言语和语言治疗、物理治疗和职业治疗。病人在四岁生日之前开始上幼儿园。在一年的随访中,患者的语言能力有了很大的提高,PEAC不再被报道。结论当骨性、脑性和脊柱性疾病伴有危及生命的呼吸障碍时,以下因素可以减少残疾的影响并促进参与:跨学科团队的治疗,辅助和康复技术的可用性,无障碍家庭生活,适合发育的环境,以及训练有素的护理人员的持续存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rehabilitation in a child with Chiari II malformation, lumbosacral meningomyelocele, achondroplasia and impaired respiratory regulation - a case report and literature review.

BackgroundChiari II malformation occurs in one of 1000 live births and causes posterior fossa malformation. In Chiari II malformation, a lumbosacral meningomyelocele is nearly always present. Achondroplasia is the most common cause of dwarfism, occurring in one of 26,000 live births. Both Chiari II malformation and achondroplasia can cause compression at the craniocervical junction and consecutive hydrocephalus.Case presentationThe case of a three-year-old male with Chiari II malformation, lumbosacral meningomyelocele, and achondroplasia is presented. To the authors' knowledge, this is the second such case that has been reported so far. A surgical therapy of a lumbosacral meningomyelocele and an implantation of a ventriculoperitoneal shunt was performed in the first month after birth. At the age of two years, occipitoatlantoaxial stenosis required spinal decompression and laminectomy. The child presented in the outpatient department with life-threatening respiratory dysregulation, comprising prolonged expiratory apnoea with cyanosis (PEAC), acquired central hypoventilation syndrome, central sleep apnoea and obstructive sleep apnoea. He also presented with delayed language development, paraplegia, a neurogenic bladder, and dwarfism. The patient received non-invasive ventilation and had an individually adapted set of assistive and therapeutic devices. Cough insufficiency necessitated the adaption of mechanical insufflation-exsufflation. Speech and language therapy, physiotherapy, and occupational therapy were performed regularly. The patient started attending kindergarten just before his fourth birthday. At his one year follow-up, the patient's language capacities substantially improved and PEAC was not reported anymore.ConclusionWhen osseous, cerebral, and spinal disease are accompanied by life-threatening respiratory impairment, the following factors can reduce the impact of disability and can foster participation: treatment by an interdisciplinary team, the availability of assistive and rehabilitative technologies, living in a barrier-free home, a developmentally appropriate environment, and the continuous presence of trained caregivers.

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来源期刊
CiteScore
2.30
自引率
5.30%
发文量
139
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