Evidence map›Paper›PMID 41832921›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

New insights into enlarged parietal foramina: an anatomical, radiological, and histological study.

Laurel A Seltzer, Brianna L Hines, Zachary S Weisberg, David Ezra, Joseph Lockwood, Hotaka Kawai, Noritaka Komune, Joe Iwanaga, Aaron S Dumont, R Shane Tubbs

Abstract read
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Laurel A SeltzerTulane University School of Medicine, New Orleans, LA, USA.
Brianna L HinesTulane University School of Medicine, New Orleans, LA, USA.
Zachary S WeisbergTulane University School of Medicine, New Orleans, LA, USA.
David EzraSchool of Nursing Sciences, The Academic College of Tel Aviv Jaffa, Tel Aviv Jaffa, Israel.
Joseph LockwoodDepartment of Neurosurgery, Clinical Neuroscience Research Center, Tulane University School of Medicine, New Orleans, LA, USA.
Hotaka KawaiDepartment of Oral Pathology and Medicine, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Noritaka KomuneDepartment of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Joe IwanagaDepartment of Neurosurgery, Clinical Neuroscience Research Center, Tulane University School of Medicine, New Orleans, LA, USA. iwanagajoeca@gmail.com.
Aaron S DumontDepartment of Neurosurgery, Clinical Neuroscience Research Center, Tulane University School of Medicine, New Orleans, LA, USA.
R Shane TubbsDepartment of Neurosurgery, Clinical Neuroscience Research Center, Tulane University School of Medicine, New Orleans, LA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEnlarged parietal foramina (EPF) are rare, symmetric calvarial defects. Although typically benign, they are clinically significant due to possible associations with venous malformations and inherited genetic variants. However, the anatomical, radiological, and histological details of these entities are scant in the medical literature.

methodsTwo hundred and fifty adult human skulls from multiple anatomical collections were examined for EPF. Gross morphometric data were supplemented by high-resolution microcomputed tomography (microCT) and histological analysis (H&E, PAS, and Masson's trichrome). Morphology, cortical continuity, and edge characteristics were evaluated to distinguish developmental defects from acquired bone lesions.

resultsBilateral EPF were identified in two (0.8%) specimens. MicroCT revealed smooth, corticated margins without lytic or reactive changes. Histological sections demonstrated abrupt cortical thinning and fibrovascular connective tissue at the defect edge, without evidence of osteoclastic activity, inflammation, or abnormal deposition. Surrounding bone exhibited normal cortical and trabecular architecture.

conclusionOur findings support the theory that EPF represents a localized congenital ossification defect of the parietal bone rather than a pathologic erosion. Their developmental origin likely reflects aberrant parietal notch closure and persistent falcine venous structures. Understanding their embryologic and genetic basis enhances clinical recognition, guides genetic counseling, and informs surgical management strategies.

Indexed as

Parietal BoneAdultEncephaloceleFemaleHumansMaleX-Ray MicrotomographyAnatomyBoneCalvariaCongenitalCraniumDefectSkull

Identifiers

PMID41832921
PMCPMC12989460

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.