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带寰前弓发育不良的颅底凹陷症 3 型(pedunculated Chiari 3 malformation with proatlas defect)。

Pedunculated Chiari 3 malformation with proatlas defect.

机构信息

Department of Neurosurgery, IMS and SUM Hospital, SOA University, Kalinga Nagar, Bhubaneswar, India.

Department of Anesthesia, IMS and SUM Hospital, SOA University, Kalinga Nagar, Bhubaneswar, India.

出版信息

Childs Nerv Syst. 2023 Dec;39(12):3613-3616. doi: 10.1007/s00381-023-06044-6. Epub 2023 Jun 27.

Abstract

Chiari III malformation is considered to be a rare congenital abnormality in human with very high mortality rates. Seventy percent of Chiari III is found to be associated with C1 arch defect as reported by Cakirer (Clin Imaging 27:1-4, 2003). The herniation of posterior fossa elements or dysplastic neural tissue is a must to stamp it as Chiari 3 malformation. The malformation is a result of the abnormal development of craniovertebral junction (CVJ). The CVJ developed from the occipital somites and the first spinal sclerotome. The major role in the development of the CVJ is played by the fourth occipital somite, which is otherwise known as "proatlas." The Chiari III anomalies are due to a result of proatlas defect, which results from failures of segmentation, failures of fusion of different components of each bone, or hypoplasia and ankylosis. We are presenting a case of a 1-year 4-month-old female child who presented with pedunculated swelling at the suboccipital region. The swelling was cystic and with pulsation. On evaluation, we found Chiari III anomaly with C1 posterior arch deficiency (proatlas defect). He was surgically managed. The outcome of the patient was good. Despite literature concluding Chiari 3 malformation with an unfavorable outcome, however, meticulous management and good pre- and postoperative care, physical therapy, and follow-up are necessary for good outcome.

摘要

Chiari III 畸形被认为是人类中一种罕见的先天性异常,死亡率非常高。Cakirer 曾报道(Clin Imaging 27:1-4, 2003),70%的 Chiari III 与 C1 弓缺陷有关。后颅窝结构的疝出或发育不良的神经组织是 Chiari 3 畸形的必要特征。这种畸形是颅颈交界区(CVJ)异常发育的结果。CVJ 由枕骨体节和第一个脊柱软骨体节发育而来。第四枕骨体节在 CVJ 的发育中起着主要作用,也被称为“原寰椎”。Chiari III 异常是由于原寰椎缺陷引起的,这是由于每个骨的不同成分的分割失败、融合失败、发育不全和骨化不良所致。我们报告了一例 1 岁 4 个月大的女性患儿,其枕骨下区有带蒂肿胀。肿胀呈囊性,有搏动。评估发现 Chiari III 异常,伴有 C1 后弓缺损(原寰椎缺陷)。患儿接受了手术治疗。患儿预后良好。尽管文献结论认为 Chiari 3 畸形预后不佳,但需要进行细致的管理和良好的术前、术后护理、物理治疗和随访,以获得良好的预后。

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