Intracranial Volume Post Cranial Expansion Surgery Using Three-Dimensional Computed Tomography Scan Imaging in Children With Craniosynostosis

被引:6
作者
Sulong, Shukriyah [1 ,2 ]
Alias, Azmi [1 ]
Johanabas, Fadzlishah [1 ]
Abdullah, Johari Yap [3 ]
Idris, Badrisyah [2 ]
机构
[1] Hosp Kuala Lumpur, Dept Neurosurg, Jalan Pahang Wilayah Persekutuan, Kuala Lumpur 50586, Malaysia
[2] Univ Sains Malaysia, Sch Med Sci, Dept Neurosci, Kota Baharu, Kelantan, Malaysia
[3] Univ Sains Malaysia, Craniofacial Med Imaging Cluster Res & Innovat U, Sch Dent Sci, Kota Baharu, Kelantan, Malaysia
关键词
3D CT scan; children; Cranial vault reshaping; Craniosynostosis; Fronto-orbital advancement; Intracranial volume; SINGLE-SUTURE CRANIOSYNOSTOSIS; SURGICAL-TREATMENT; PRESSURE; NEURODEVELOPMENT; RADIOGRAPHS; MANAGEMENT;
D O I
10.1097/SCS.0000000000005810
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Craniosynostosis is a congenital defect that causes >= 1 suture to fuse prematurely. Cranial expansion surgery which consists of cranial vault reshaping with or without fronto-orbital advancement (FOA) is done to correct the skull to a more normal shape of the head as well as to increase the intracranial volume (ICV). Therefore, it is important to evaluate the changes of ICV after the surgery and the effect of surgery both clinically and radiologically. Objective: The aim of this study is to evaluate the ICV in primary craniosynostosis patients after the cranial vault reshaping with or without FOA and to compare between syndromic and nonsyndromic synostosis group, to determine factors that associated with significant changes in the ICV postoperative, and to evaluate the resolution of copper beaten sign and improvement in neurodevelopmental delay after the surgery. Methods: This is a prospective observational study of all primary craniosynostosis patients who underwent operation cranial vault reshaping with or without FOA in Hospital Kuala Lumpur from January 2017 until Jun 2018. The ICV preoperative and postoperative was measured using the 3D computed tomography (CT) imaging and analyzed. The demographic data, clinical and radiological findings were identified and analyzed. Results: A total of 14 cases (6 males and 8 females) with 28 3D CT scans were identified. The mean age of patients was 23 months. Seven patients were having syndromic synostosis (4 Crouzon syndromes and 3 Apert syndromes) and 7 nonsyndromic synostosis. The mean preoperative ICV was 880mL (range, 641-1234 mL), whereas the mean postoperative ICV was 1081mL (range, 811-1385 mL). The difference was 201mL which was statistically significant (P < 0.001). In comparison, the mean volume increment for syndromic synostosis and nonsyndromic synostosis was 282 mL and 120 mL, respectively. The difference was statistically significant (P < 0.004). Three months post-operation, the copper beaten sign was still present in the CT scan which was statistically not significant in this study (P > 1.0). However, there was 100% (n = 13) improvement of this copper beaten sign. However, the neurodevelopmental delay showed no improvement which was statistically not significant (P > 1.0). Conclusion: Surgery in craniosynostosis patient increases the ICV besides it improves the shape of the head. From this study, the syndromic synostosis had better increment of ICV compared to nonsyndromic synostosis.
引用
收藏
页码:46 / 50
页数:5
相关论文
共 22 条
  • [1] Abbas Nejad E, 2010, IRAN J CHILD NEUROL, V3, P45
  • [2] Significance of beaten copper appearance on skull radiographs in children with isolated sagittal synostosis
    Agrawal, Deepak
    Steinbok, Paul
    Cochrane, D. Douglas
    [J]. CHILDS NERVOUS SYSTEM, 2007, 23 (12) : 1467 - 1470
  • [3] Pre- and postoperative developmental attainment in sagittal synostosis
    Bellew, M
    Chumas, P
    Mueller, R
    Liddington, M
    Russell, J
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 2005, 90 (04) : 346 - 350
  • [4] Hydrocephalus and craniosynostosis
    Cinalli, G
    Sainte-Rose, C
    Kollar, EM
    Zerah, M
    Brunelle, F
    Chumas, P
    Arnaud, E
    Marchac, D
    Pierre-Kahn, A
    Renier, D
    [J]. JOURNAL OF NEUROSURGERY, 1998, 88 (02) : 209 - 214
  • [5] Cohen SR, 2004, PLAST RECONSTR SURG, V114, P841, DOI 10.1097/01.PRS.0000132854.14237.A8
  • [6] Complications in the surgical treatment of craniosynostosis and craniofacial syndromes: apropos of 306 transcranial procedures
    Esparza, Javier
    Hinojosa, Jose
    [J]. CHILDS NERVOUS SYSTEM, 2008, 24 (12) : 1421 - 1430
  • [7] MITK Diffusion Imaging
    Fritzsche, K. H.
    Neher, P. F.
    Reicht, I.
    van Bruggen, T.
    Goch, C.
    Reisert, M.
    Nolden, M.
    Zelzer, S.
    Meinzer, H. -P.
    Stieltjes, B.
    [J]. METHODS OF INFORMATION IN MEDICINE, 2012, 51 (05) : 441 - 448
  • [8] Clinical outcome of the modified pi-plasty procedure for sagittal synostosis
    Guimaraes-Ferreira, J
    Gewalli, F
    David, L
    Olsson, R
    Friede, H
    Lauritzen, CGK
    [J]. JOURNAL OF CRANIOFACIAL SURGERY, 2001, 12 (03) : 218 - 224
  • [9] Craniosynostosis
    Johnson, David
    Wilkie, Andrew O. M.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (04) : 369 - 376
  • [10] Growth curves for intracranial volume in normal Asian children fortify management of craniosynostosis
    Kamochi, Hideaki
    Sunaga, Ataru
    Chi, Daekwan
    Asahi, Rintaro
    Nakagawa, Shiho
    Mori, Masanori
    Uda, Hirokazu
    Sarukawa, Shunji
    Sugawara, Yasushi
    Yoshimura, Kotaro
    [J]. JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY, 2017, 45 (11) : 1842 - 1845