Literature DB >> 20186071

Associated (parallel) tomographic findings in patients with single-sutural synostosis.

Renato da Silva Freitas1, Thais de Freitas Azzolini, Joseph H Shin, John A Persing.   

Abstract

INTRODUCTION: Craniosynostosis is the premature fusion of 1 or more of the cranial sutures, which causes an abnormal skull shape. The treatment is complex and requires surgical intervention for correction, between 3 and 12 months of age. The current standard for diagnosing craniosynostosis is to obtain a computed tomographic (CT) scan. However, recent studies have emphasized potential problems associated with ionizing radiation. The aim of this study was to evaluate the use of the preoperative CT scan, and its findings, and to define the value of these data.
MATERIALS AND METHODS: This study is a retrospective analysis of 89 patients with craniosynostosis during the period between 1998 and 2007, who had CT using the Yale-New Haven Hospital computer system. Clinical findings such as age, sex, and diagnosis were recorded. All intraoperative abnormalities were noted. Preoperative CT scans were reevaluated for accuracy and completeness of diagnosis, cerebral anomalies, and other head and neck pathologic conditions.
RESULTS: Initially, 131 cases of nonsyndromic craniosynostosis were identified. Of these, we had access to CT evaluations in 89 patients. The mean age at the time of the surgery was 13 months, varying from 2 months to 18 years old. Most patients were males. The most common diagnoses were sagittal synostosis in 47 cases; unilateral coronal, 16; and metopic, 15. In most patients, the CT scan demonstrated the same diagnosis as the clinical examination-derived diagnosis. However, 6 patients had an incomplete diagnosis or misdiagnosis. In addition, 3 cases of prominence of the subarachnoid space, 2 cases of cerebral atrophy, 1 case of subarachnoid tumor, and 1 deformational dysplasia of encephalon were identified. Other minor additional diagnoses were 5 cases of fluid in the middle ear and antrum of mastoid, 2 cases of cysts in the maxilla, and 1 case of an associated cervical lymphatic tumor.
CONCLUSIONS: The advantage of CT use is greater accuracy in diagnosis, less potential for inappropriate surgery, and, as an ancillary effect, a more complete and timely assessment of congenital anomalies so that more appropriate referrals can be made. Low-dose (pediatric) radiation CT still seems to have a place in the examination of a patient with skull deformity and potential craniosynostosis.

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Year:  2010        PMID: 20186071     DOI: 10.1097/SCS.0b013e3181cfa7ad

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  3 in total

Review 1.  Skull base development and craniosynostosis.

Authors:  Susan I Blaser; Nancy Padfield; David Chitayat; Christopher R Forrest
Journal:  Pediatr Radiol       Date:  2015-09-07

2.  A new three-dimensional measurement in evaluating the cranial asymmetry caused by craniosynostosis.

Authors:  Hongyu Yin; Xue Dong; Bin Yang
Journal:  Surg Radiol Anat       Date:  2015-01-25       Impact factor: 1.246

3.  Comparing the Use of 3D Photogrammetry and Computed Tomography in Assessing the Severity of Single-Suture Nonsyndromic Craniosynostosis.

Authors:  Olivia A Ho; Nikoo Saber; Derek Stephens; April Clausen; James Drake; Christopher Forrest; John Phillips
Journal:  Plast Surg (Oakv)       Date:  2017-04-28       Impact factor: 0.947

  3 in total

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