Scaphocephaly

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Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture. Premature closure results in limited lateral expansion of the skull, resulting in a characteristic long, narrow head.<ref>Template:Citation</ref> The skull base is typically spared.<ref>Template:Cite journal</ref> The word comes Template:Ety.

Scaphocephaly is the most common of the craniosynostosis conditions and accounts for approximately 50% of all craniosynostosis.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> It is most commonly idiopathic (non-syndromic).

EtiologyEdit

Non-syndromic

The underlying cause of the non-syndromic form is unknown. Over 100 mutations have been associated, including mutations in the FGFR genes.<ref>Template:Cite journal</ref> Several potential risk factors have been identified for craniosynostosis include:<ref>Template:Cite journal</ref>

Advanced maternal age
White maternal race
Maternal smoking
Male infant
Certain paternal occupations (e.g. agriculture, forestry, repairmen) <ref>Template:Cite journal</ref>

Syndromic

Sagittal craniosynostosis is seen in many conditions and syndromes:<ref name="NCBI">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Acrocephalosyndactyly type I
Baller–Gerold syndrome
Cardiocranial syndrome, Pfeiffer type
Coffin-Siris syndrome 7
Cranioectodermal dysplasia 1, 3, and 4
Craniosynostosis (nonsyndromic) 4
Craniosynostosis and dental anomalies
Craniosynostosis-anal anomalies-porokeratosis syndrome
Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
Crouzon syndrome
Meier-Gorlin syndrome 7
Neonatal diabetes mellitus with congenital hypothyroidism
Noonan syndrome 3
RAB23-related Carpenter syndrome
Syndactyly type 1 (Chromosome 2q35 Duplication Syndrome)
Tatton-Brown–Rahman syndrome
TCF12-related craniosynostosis
Teebi hypertelorism syndrome 1
Trigonocephaly-short stature-developmental delay syndrome
TWIST1-related craniosynostosis

Diagnosis and evaluationEdit

Diagnosis of scaphocephaly is with physical exam, which may show characteristic features such as an elongated head in the anterior-posterior dimension, narrow head in the lateral dimension, and bony ridge at the vertex.<ref name="Sandoval-2022">Template:Citation</ref>

Further evaluation with imaging may also be performed. Ultrasound may be used to detect fusion of the suture. CT scans may also be used to help with surgical planning and to diagnose associated hydrocephalus, which has been found to be present in 44% of cases in one study.<ref>Template:Cite journal</ref> A measure of cephalic index may also be reduced, however the reliability of measurements may not be a reliable measure.<ref>Template:Cite journal</ref>

ClassificationEdit

Scaphocephaly can be classified into specific types, depending on morphology, position, and suture closure:<ref>Template:Cite journal</ref>

Bathrocephaly– bulging of the mid-section of the occipital bone; also associated with isolated mendosal suture synostosis.<ref>{{#invoke:citation/CS1|citation

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Clinocephaly– flat cranium due to loss of cranial convexity;<ref name=":0">Template:Cite journal</ref> top of head is depressed inwards.<ref>Template:Cite journal</ref>
Dolichocephaly– long and narrow head.<ref>{{#invoke:citation/CS1|citation

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Leptocephaly– synostosis extends down to the metopic suture;<ref>Template:Cite journal</ref> the head becomes narrow, but tall rather than long.<ref name=":0" />
Sphenocephaly– wedge-shaped head.<ref>Template:Citation</ref>

Dolichocéphalie a 10 ans.jpg

Dolichocephaly
Shuttleworth Potts Plate VII (1).jpg

Leptocephaly
Various types 2 (detail E, sphenocephalus).jpg

Sphenocephaly

TreatmentEdit

This condition can be corrected by surgery if the child is young enough, typically within the first 3–6 months.<ref name="Sandoval-2022" /> The goal of treatment is to correct intracranial pressure and repair bony deformities.<ref>Template:Cite journal</ref> The decision to treat is multifactorial and should be performed at a center with an experienced craniofacial team.<ref name="Buchanan-2017">Template:Cite journal</ref> In addition to the primary craniofacial surgeon, team members may include audiologists, dentists, otolaryngologists, neurosurgeons, plastic surgeons, and other supporting members.<ref name="Buchanan-2017" />

Surgery is generally aimed at removal of the fused sagittal suture to allow for lateral expansion of the skull. Surgical options include:<ref name="Sandoval-2022" />

Endoscopic strip craniectomy: Minimally invasive removal of the fused suture. Following surgery, patients typically wear a helmet to help shape the head. Helmets are usually worn for 3–12 months.<ref>{{#invoke:citation/CS1|citation

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Open cranial vault remodeling: Open surgical removal of the fused sagittal suture and re-shaping of the skull, generally with resorbable plates.<ref>Template:Cite journal</ref>
Spring cranioplasty: Combination of an endoscopic strip craniectomy with placement of springs which provide continuous force for re-shaping the skull.<ref>{{#invoke:citation/CS1|citation

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TerminologyEdit

The term, from Greek skaphe meaning 'light boat or skiff' and kephale meaning 'head', describes a specific shape of a long narrow head<ref>Template:DorlandsDict</ref> that resembles a boat.