异位缝合性滑膜闭锁(三角头)1例报告

E. Bal, Ismail Bozkurt, Cevat Akıncı, N. Yılmaz
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引用次数: 0

摘要

颅缝闭锁是一种单个或多个颅缝的过早融合。每2000-2500例活产婴儿中就有一例发生三角头症(1,2)。三角头症是一种颅缝闭锁,由分隔两个额骨的异位缝合线过早融合和骨化引起,并在3 - 8个月大时生理闭合(3,4)。1862年,韦克尔首次描述了三角头症,它是一个希腊语术语,意思是三角形的前额。异位性骨膜闭锁发生在新生儿的1/700到1/ 15000之间(5,6)。这导致颅骨呈三角形前额,外侧眶缘缺失,增加眶上后缩和双颞凹陷。生长受限导致颅内容积减小。因此,手术干预可以恢复颅骨的体积和外观(7)。本研究旨在报道一名出生时患有三叉头畸形的儿童,在6个月大时进行双额开颅和额眶前移手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metopic Suture Synostosis ( Trigonocephaly ) : A Case Report
Craniosynostosis is a premature fusion of single or multiple cranial sutures. It occurs in one of 2000–2500 live births (1, 2). Trigonocephaly is a form of craniosynostosis arising from the premature fusion and ossification of the metopic suture, which separates the two frontal bones and physiologically closes at 3–8 months of age (3, 4). Described first by Welcker in 1862, trigonocephaly is a Greek term meaning triangular forehead. Metopic synostosis occurs in between 1/700 and 1/15.000 newborns (5, 6). This results in a skull with a triangular forehead and deficient lateral orbital rims add to the supraorbital retrusion and bitemporal indentations. The growth restriction results in decreased intracranial volume. Thus, a surgical intervention is indicated to restore the volume of the skull along with appearance (7). This study aimed to present the case of a child born with trigonocephaly who was operated at 6 months of age with bifrontal craniotomy and fronto-orbital advancement.
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