2009
DOI: 10.1097/scs.0b013e31819b9627
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Surgical Treatment for Scaphocephaly and a Calcified Cephalohematoma

Abstract: Craniosynostosis is the premature fusion of 1 or more of the cranial sutures, with sagittal synostosis being the most common nonsyndromic single suture synostosis. The pathogenesis of craniosynostosis has been extensively studied and is likely multi-factorial. A complex interaction between the dura and overlying suture via multiple growth factors seems to play the most important role. There have been 3 published studies with patients presenting with scaphocephaly and a cephalohematoma, which raises the questio… Show more

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Cited by 12 publications
(4 citation statements)
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“…Currarino 5 supported this interpretation. The case reported by Kortesis et al 10 is not relevant in so much as the ossified cephalohematoma was off the midline and did not cross the sagittal suture. Observations from the 2 cases presented here support the conclusion that sagittal synostosis has a causal relationship with development of a midline hematoma and not vice versa.…”
mentioning
confidence: 92%
“…Currarino 5 supported this interpretation. The case reported by Kortesis et al 10 is not relevant in so much as the ossified cephalohematoma was off the midline and did not cross the sagittal suture. Observations from the 2 cases presented here support the conclusion that sagittal synostosis has a causal relationship with development of a midline hematoma and not vice versa.…”
mentioning
confidence: 92%
“…Over time, the bulge may feel harder as the collected blood calcifies. If that hematoma had not been treated, albeit rarely, large calcified cephalohematomas would need surgical treatment with a certain probability [10][11]. Thus, appropriate treatment methods are desired.…”
Section: Discussionmentioning
confidence: 99%
“…3 Other indications may be the prevention of brain growth restriction, and diagnostic confirmation and treatment of associated craniosynostosis. 11,13,15,16 Surgery is performed according to the features of the CC. Type I CC is treated by drilling of the outer lamella, whereas Type 2 is treated by craniotomy and cranioplasty.…”
Section: Discussionmentioning
confidence: 99%
“…29 However, sagittal synostosis secondary to cephalohematoma has been described. 11,15,16 We report the case of an 11-year-old girl with a CC that caused late-onset cerebral electrical anomalies. To the best of our knowledge, this complication was not been described to date in the literature.…”
mentioning
confidence: 99%