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先天性肌性斜颈合并矢状缝早闭:一例报告

Congenital muscular torticollis concurrent with sagittal synostosis: a case report.

作者信息

Kim Seung-Hyun, Ahn Ah-Reum, Yim Shin-Young

机构信息

The Clinic for Torticollis, Department of Physical Medicine and Rehabilitation, Ajou University School of Medicine, Suwon, Korea.

出版信息

Ann Rehabil Med. 2014 Oct;38(5):712-6. doi: 10.5535/arm.2014.38.5.712. Epub 2014 Oct 30.

Abstract

Congenital muscular torticollis (CMT) and craniosynostosis are diseases that cause plagiocephaly and craniofacial asymmetry in children. In our literature review, we did not find any report of concurrent manifestation of CMT and craniosynostosis. A 41-month-old boy visited our hospital with left torticollis, right laterocollis, and craniofacial asymmetry as the main findings. During clinical examination, prominent right sternocleidomastoid muscle and limited range of motion of the neck were noted, and right CMT was confirmed by magnetic resonance imaging of the neck. Three-dimensional computed tomography of the skull, which was conducted due to the unusual appearance of the skull with a large head circumference, mild brachycephaly, as well as left plagiocephaly, revealed premature closure of the sagittal suture. Thus, we report the first case that showed concurrence of CMT and sagittal synostosis. We recommend that concurrently manifested craniosynostosis needs to be examined if the subject with CMT displays unusual craniofacial asymmetry to a greater extent than deformational plagiocephaly.

摘要

先天性肌性斜颈(CMT)和颅缝早闭是导致儿童斜头畸形和颅面不对称的疾病。在我们的文献综述中,未发现任何关于CMT和颅缝早闭同时出现的报告。一名41个月大的男孩因以左侧斜颈、右侧颈侧弯和颅面不对称作为主要表现前来我院就诊。临床检查时,发现右侧胸锁乳突肌突出且颈部活动范围受限,颈部磁共振成像证实为右侧CMT。由于头颅外观异常,表现为头围大、轻度短头畸形以及左侧斜头畸形,遂进行了头颅三维计算机断层扫描,结果显示矢状缝过早闭合。因此,我们报告了首例CMT与矢状缝早闭同时出现的病例。我们建议,如果患有CMT的患者出现的颅面不对称程度超过变形性斜头畸形,需对同时存在的颅缝早闭进行检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f13/4221403/dc11ddd07c1c/arm-38-712-g001.jpg

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