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首页> 外文期刊>The Journal of craniofacial surgery >Benign Radiographic Coronal Synostosis After Sagittal Synostosis Repair
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Benign Radiographic Coronal Synostosis After Sagittal Synostosis Repair

机译:矢状突突修复后的良性影像学冠状动脉突触

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摘要

Whether cranial vault remodeling surgery for nonsyn-dromic, isolated sagittal suture synostosis affects the patency of initially normal, unaffected sutures is unknown. The influence of coronal and lambdoidal suture patency after cranial vault remodeling on the trajectory of subsequent cranial growth is also unknown. Disruption of normal sutural anatomy during cranial vault reconstruction could influence the incidence of secondary craniosynosto-sis and need for reoperation in a small proportion of these patients.We performed a retrospective review of patients younger than 1 year with nonsyndromic sagittal synostosis treated at a single tertiary referral pediatric hospital from September 2005 to January 2010 by an interdisciplinary team. Computed tomographic images obtained preoperatively, immediately postoperatively, and 2 years postoperatively were evaluated for the occurrence of secondary synostosis of initially nonsynostotic sutures. Craniofacial disorders clinic and ophthalmologic follow-up records were also analyzed for the occurrence of radiographic cranial restenosis, clinical or ophthalmologic signs of intracranial hypertension (ICH), and reoperation.Fifty-one patients younger than 1 year underwent primary surgical repair of isolated, nonsyndromic sagittal suture synostosis during the study period. Thirty-seven of these patients (71%) had completed 2-year clinical and radiographic follow-up by the time of analysis, constituting the study population. The average age at surgery was 5.4 months (range, 3.1-11.5 months). Thirty-three (89%) of the 37 study patients showed radiographic evidence of bilateral secondary coronal synostosis (SCS). Five patients (15%) additionally showed partial lambdoid synostosis. One patient with radiographic SCS (3%) required reoperation for radiographic cranial restenosis, clinical signs and symptoms of ICH, and papilledema first noted 1 year after primary cranial vault reconstruction.
机译:对于非综合征性,分离的矢状缝线骨膜增生的颅穹改建手术是否会影响最初正常的,未受影响的缝线的通畅性尚不清楚。颅穹改建后冠状和Lambdoidal缝线通畅对随后颅骨生长轨迹的影响也是未知的。颅内穹reconstruction重建过程中正常缝隙解剖结构的破坏可能会影响继发性颅囊吻合术的发生率,并且需要对这些患者中的一小部分进行再手术。我们对单龄三岁以下合并非综合征性矢状突触的小于1岁患者进行了回顾性研究。 2005年9月至2010年1月,由一个跨学科团队转诊到儿科医院。评估术前,术后立即和术后2年获得的计算机断层图像,以评估最初的非骨突缝合线继发性骨突的发生情况。还对颅面疾病门诊和眼科随访记录进行了分析,以了解放射影像性颅内再狭窄的发生,颅内高压(ICH)的临床或眼科体征以及再手术的情况。年龄小于1岁的51例患者接受了孤立的,非综合症的初次手术修复在研究期间矢状缝线骨突形成。截至分析时,这些患者中有37名(71%)已完成2年的临床和影像学随访,构成了研究人群。手术的平均年龄为5.4个月(范围3.1-11.5个月)。在37名研究患者中,有33名(89%)表现出了双侧继发性冠状动脉突触(SCS)的影像学证据。 5例患者(15%)还显示出部分lambdoid突触。一名放射状SCS患者(3%)因放射状颅再狭窄,ICH的临床体征和症状以及首次颅内穹ault重建一年后首次注意到的乳头水肿而需要再次手术。

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