Magnetic Resonance Imaging in Isolated Sagittal Synostosis
Abstract
Isolated fusion of the sagittal suture is the most prevalent form of craniosynostosis. Although the typical clinical appearance usually points the way to the right diagnosis, computed tomographic (CT) scans are still recommended as necessary tools for both the diagnosis of scaphocephaly and the preoperative planning. Because CT scans are accompanied by the biological effects of ionizing radiation, some authors have already postulated the use of magnetic resonance imaging (MRI) especially because MRI seems to be valuable for detecting intracranial anomalies compared with CT scans. Hence, we investigated the preoperative MRIs of 42 children with isolated sagittal synostosis to evaluate the frequency of brain anomalies and their therapeutic consequences.In our study, 10 patients (23.8%) showed pathologic MRI findings such as ventricular dilatation and hypoplastic corpus callosum, whereas 32 patients (76.2%) had an unremarkable MRI except a pathognomonic secondary deformation of the brain caused by the abnormally shaped skull, which was present in all patients. Seven patients showed clinically significant symptoms including papilledema or psychomotoric developmental delay; however, the clinical appearance was not predictive for pathologic MRI findings and vice versa.As the detection of brain anomalies had no influence on the surgical procedure or led to any additive therapy in our patients, we conclude that evaluation of possible pathologic brain findings does not legitimate the general use of MRI in clinically normal children with isolated sagittal synostosis.
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Eley et al. examined 'black bone MRI', which enables precise cranial suture assessment without radiation but necessitates anaesthesia in young children.
“Eley et al. examined the “black bone MRI”, which enables precise cranial suture assessment without radiation but necessitates anaesthesia in young children [5, 32, 33]”
From Developments in diagnostic and surgical techniques in children with sagittal suture craniosynostosis: a systematic review spanning the last 30 years (2025) · cites this paper as [33]
Cites
Single Sutural Craniosynostoses: Surgical Outcomes and Long-Term Growth
Fearon, J. A., Ruotolo, R. A., & Kolar, J. C. (2009) · Plastic and Reconstructive Surgery · doi:10.1097/prs.0b013e318195661a · Cited by 196 · see citing works
Hydrocephalus in craniosynostosis: a review
Collmann, H., Sörensen, N., & Krauß, J. (2005) · Child s Nervous System · doi:10.1007/s00381-004-1116-y · Cited by 192 · see citing works
Retrospective Study of Nonsyndromic Craniosynostosis Treated Over a 10-Year Period
Breugem, C. C., & Zeeman, B. J. V. R. (1999) · Journal of Craniofacial Surgery · doi:10.1097/00001665-199903000-00010 · Cited by 53 · see citing works
Maxillary Dental Development in Complete Unilateral Alveolar Clefts
Solis, A., Figueroa, A. A., Cohen, M., Polley, J. W., & Evans, C. A. (1998) · The Cleft Palate-Craniofacial Journal · doi:10.1597/1545-1569(1998)035 · Cited by 51 · see citing works
Jane, J. A., Lin, K. Y. K., & Jane, J. A. (2000) · Neurosurgical FOCUS · doi:10.3171/foc.2000.9.3.4 · Cited by 46 · see citing works
Computed tomographic evaluation of corpus callosum agenesis and associated malformations
Larsen, P. D., & Osborn, A. G. (1982) · Journal of Computed Tomography · doi:10.1016/0149-936x(82)90036-4 · Cited by 30 · see citing works
Treatment of sagittal synostosis: Subtotal cranial vault remodelling with right-angled Z-osteotomies
Moon, S., Paik, H. W., & Byeon, J. H. (2010) · Journal of Plastic Reconstructive & Aesthetic Surgery · doi:10.1016/j.bjps.2009.11.006 · Cited by 12 · see citing works
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Eley, K. A., Watt-Smith, S. R., Sheerin, F., & Golding, S. J. (2014) · European Radiology · doi:10.1007/s00330-014-3286-7 · Cited by 136 · see citing works
Clinical and neuroradiological features of the 9p deletion syndrome
Spazzapan, P., Arnaud, É., Baujat, G., Nizon, M., Malan, V., Brunelle, F., & Rocco, F. D. (2015) · Child s Nervous System · doi:10.1007/s00381-015-2957-2 · Cited by 62 · see citing works
Thiele-Nygaard, A. E., Foss-Skiftesvik, J., & Juhler, M. (2020) · Child s Nervous System · doi:10.1007/s00381-020-04502-z · Cited by 36 · see citing works
The Etiology of Neuronal Development in Craniosynostosis: A Working Hypothesis
Brooks, E. D., Beckett, J. S., Yang, J. F., Timberlake, A. T., Sun, A. H., Chuang, C., & Persing, J. A. (2017) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000004040 · Cited by 32 · see citing works
Normalization of brain morphology after surgery in sagittal craniosynostosis
Brooks, E. D., Yang, J. F., Beckett, J. S., Lacadie, C., Scheinost, D., Persing, S. M., Zellner, E., Oosting, D., Keifer, C. M., Friedman, H. E., et al. (2015) · Journal of Neurosurgery Pediatrics · doi:10.3171/2015.7.peds15221 · Cited by 32 · see citing works
Dolichocephaly Without Sagittal Craniosynostosis
Beckett, J. S., Pfaff, M. J., DiLuna, M. L., & Steinbacher, D. M. (2013) · Journal of Craniofacial Surgery · doi:10.1097/scs.0b013e3182a12ece · Cited by 9 · see citing works
Isolierte, nichtsyndromale Kraniosynostosen
Freudlsperger, C., Castrillon‐Oberndorfer, G., Hoffmann, J., & Engel, M. (2013) · Der MKG-Chirurg · doi:10.1007/s12285-013-0364-9 · Cited by 7 · see citing works
Self-citationZöller, J. E., & Kreppel, M. (2021) · Springer eBooks · doi:10.1007/978-3-662-58984-7_13 · Cited by 4 · see citing works
Hermann, J., Raak, C. K., Ostermann, T., & Scharbrodt, W. (2025) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-025-03978-9 · Cited by 2 · see citing works
“…the “black bone MRI”, which enables precise cranial suture assessment without radiation but necessitates anaesthesia in young children [5, 32, 33], while sonography up to 13 months of age can distinguish an open from a closed suture with a reported sensitivity of 100% and specificity of…”
Guida, L., Gardin, A., James, S., Arnaud, É., Toujouse, C., Roux, J., Barreau, E., Abdallah, M. B., Almes, M., Sartori, L., et al. (2025) · Neurosurgical FOCUS · doi:10.3171/2024.10.focus24588 · Cited by 2 · see citing works
Diagnostik und Therapie isolierter Kraniosynostosen
Freudlsperger, C., Hoffmann, J., & Engel, M. (2015) · Kinder- und Jugendmedizin · doi:10.1055/s-0038-1629263 · Cited by 2 · see citing works
Self-citationYang, C. E., Park, E.-K., Lee, M., Shim, K., & Kim, Y. O. (2017) · Archives of Craniofacial Surgery · doi:10.7181/acfs.2017.18.1.21 · Cited by 2 · see citing works
Rückschloß, T., Zittel, S., Hassanein, E., Damaty, A. E., Krieg, S. M., Ristow, O., Hoffmann, J., & Engel, M. (2025) · Neurosurgical FOCUS · doi:10.3171/2024.10.focus24582 · Cited by 1 · see citing works
Self-citationIsolierte, nichtsyndromale Kraniosynostosen
Freudlsperger, C., Hoffmann, J., & Engel, M. (2018) · Der MKG-Chirurg · doi:10.1007/s12285-018-0154-5 · Cited by 1 · see citing works
Self-citationZöller, J. E., & Kreppel, M. (2023) · Springer eBooks · doi:10.1007/978-3-662-66844-3_13
Smetona, J. T., & Persing, J. A. (2024) · Cambridge University Press eBooks · doi:10.1017/9781108917339.024
- Authors
- Engel, M., Hoffmann, J., Mühling, J., Castrillón-Oberndorfer, G., Seeberger, R., & Freudlsperger, C.
- Affiliations
- University Hospital Heidelberg (DE)
- Corresponding author
- Engel, Michael
- Venue
- Journal of Craniofacial Surgery
- Published
- 2012-07
- Volume
- 23
- Issue
- 4
- Pages
- e366-e369
- ISSN
- 1049-2275 (ISSN-L)
- OpenAlex
- W2321980375
- Cited by
- 16
- References
- 7
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 1 · 2021: 1 · 2020: 1 · 2018: 1 · 2017: 2 · 2015: 3 · 2014: 1 · 2013: 2
- FWCI
- 1.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Craniofacial Surgery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Craniofacial Disorders and Treatments
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Health Sciences › Medicine › Surgery › Pectus Deformity Diagnosis and Treatment
- Keywords
- craniosynostosis, scaphocephaly, magnetic resonance imaging, brain anomalies, ventriculomegaly, hypoplastic corpus callosum, surgical planning, ionizing radiation, children, papilledema, psychomotor delay
- MeSH terms
- Cranial Sutures, Craniosynostoses, Female, Humans, Infant, Magnetic Resonance Imaging, Male, Retrospective Studies, Tomography, X-Ray Computed, Treatment Outcome
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