Cited by 9Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and TreatmentFetal and Pediatric Neurological Disorders

A systematic quantitative morpho-volumetric analysis in infants with sagittal craniosynostosis and relationship with the severity of scaphocephalic deformity

Calandrelli, Rosalinda, Pilato, Fabio, Massimi, Luca, Panfili, Marco, Colosimo, Cesare·2020·La radiologia medica

Abstract

Purpose Among patients with isolated sagittal synostosis (ISS), the head shape varies considerably in relation to the severity of the abnormality. This study aimed to quantify skull base morphometry and intracranial volume to investigate their relationships with the severity of scaphocephaly.Methods We studied 66 infants with ISS identifying three groups according to the morphological severity of cranial deformity (group I: mild deformity; group II: moderate deformity; group III: severe deformity), by combining two scaphocephaly severity indices as descriptors of the relation of three morphological measurements (length, width and height) We perform a quantitative analysis using high-resolution CT images calculating following parameters: cranial fossae dimensions, supratentorial (ICV) and infratentorial (PCFV) cranial volume, supratentorial (WBV) and infratentorial (PCFBV) brain volume, ICV/WBV, PCFV/PCFBV, supratentorial and infratentorial cerebrospinal fluid (CSF).Results In all subgroups, anterior and middle skull base lengths were increased, while posterior hemifossae lengths were unchanged. In mild subgroup, ICV/WBV was significantly different and ICV, WBV and CSF supratentorial volume increased (p < 0.05). In moderate and severe subgroups, FCPV/FCPBV was significantly different and CSF infratentorial volume was reduced (p < 0.05); FCPBV was increased only in the severe subgroup (p < 0.05).Conclusion This morpho-volumetric study provides new insights in understanding the compensatory changes occurring in infants at different stages of scaphocephaly severity. In particular, our study suggests that patients with severe deformity might have an earlier depletion of reserve mechanisms with a reduced compliance of the overall skull during encephalic growth and these patients might require early surgical cranial expansion.

Integrity signals

Registry

Crossref · 10.1007/s11547-020-01150-w

Cites

31 of 31 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Compensatory processes differ mainly according to the time of ossification of the sagittal suture in the prenatal period; early ossification is associated with a more pronounced scaphocephalic deformity, and late ossification with a less pronounced deformity.

    “It is important to point out that these compensatory processes differ mainly according to the time at which ossification of the sagittal suture takes place in the prenatal period. Thus, early ossification of the suture is associated with a more pronounced scaphocephalic deformity, whereas late ossification of the suture is associated with a less pronounced deformity [12].”

    From Isolated Sagittal Craniosynostosis: A Comprehensive Review (2024) · cites this paper as [12]

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Calandrelli, R., Pilato, F., Massimi, L., Panfili, M., & Colosimo, C.
Affiliations
Università Cattolica del Sacro Cuore (IT)
Corresponding author
Calandrelli, Rosalinda
Venue
La radiologia medica
Published
2020-02-17
Volume
125
Issue
6
Pages
585-594
ISSN
  • 0033-8362 (ISSN-L)
  • 1826-6983
OpenAlex
W3005875826
Cited by
9
References
31
Citations by year
2025: 1 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 1
FWCI
0.73
Type
journal article
Language
en
Open access
closed
Locations
  • La radiologia medica (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Craniofacial Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Pectus Deformity Diagnosis and Treatment
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
Keywords
scaphocephaly, intracranial volume, cranial volume, brain volume, cerebrospinal fluid volume, infants
MeSH terms
Craniosynostoses, Female, Humans, Infant, Male, Retrospective Studies, Severity of Illness Index, Tomography, X-Ray Computed, Skull Base, Imaging, Three-Dimensional

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review