Evidence map›Paper›PMID 42144485›Full record

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

Primary intraosseous meningioma in a child: an unusual case report and literature review.

Eleonora Visocchi, Manuel Camelia, Chiara Spezzani, Alice Noris, Anna Maria Buccoliero, Francesca Ormitti, Flavio Giordano

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In one paragraph

Review 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.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Eleonora VisocchiDepartment of Neurosurgery, AOU Careggi, University of Florence, Florence, Italy. eleonora.visocchi@unifi.it.
Manuel CameliaDepartment of Neurosurgery, AOU Careggi, University of Florence, Florence, Italy.
Chiara SpezzaniPediatric Neurosurgery and Functional and Epilespy Surgery, Meyer Children's Hospital IRCCS, Florence, Italy.
Alice NorisPediatric Neurosurgery and Functional and Epilespy Surgery, Meyer Children's Hospital IRCCS, Florence, Italy.
Anna Maria BuccolieroPathology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.
Francesca OrmittiDepartment of Neuroradiology, Parma University Hospital, Parma, Italy.
Flavio GiordanoPediatric Neurosurgery and Functional and Epilespy Surgery, Meyer Children's Hospital IRCCS, Florence, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary intraosseous meningiomas (PIOMs) are rare extradural meningiomas, originating within the skull, and accounting for approximately 2% of all meningiomas. These tumors are exceptionally uncommon in children, since the majority occurs in adults between 20 and 60 years old. Few cases have been reported in the literature, focusing on clinical findings, surgery, and outcomes in younger people. We report a case of a 9-year-old female with progressive painful frontal skull bossing, without neurological symptoms. Magnetic resonance imaging (MRI) diagnosed an osteolytic lesion in the right paramedian frontal bone. Surgery achieved gross total resection of the lesion, characterized by a clear cleavage plane from the surrounding bone with no dural involvement but infiltrating the upper wall of the frontal sinus. The skull defect was repaired with a three-dimensional (3D) custom-made titanium cranioplasty that provided an excellent aesthetic outcome. Histology revealed a primary intraosseous meningioma. Surgical resection is the cornerstone of PIOM treatment, offering high rates of gross total resection with low morbidity and no reported mortality. Our approach confirms the feasibility of complete resection along with cranial reconstructive techniques to optimize functional and aesthetic outcomes. We compare our findings with the limited literature data on pediatric PIOMs, discussing surgical strategies and outcomes in terms of disease control and aesthetic results. This case highlights the unique challenges of diagnosis and management of PIOMs in children, emphasizing the importance of radical removal along with excellent cosmetic results.

Indexed as

Meningeal NeoplasmsMeningiomaSkull NeoplasmsChildFemaleHumansMagnetic Resonance ImagingBone tumor resectionIntradiploic lesionPediatric meningiomaPrimary intraosseous meningiomaRare cranial tumorsSkull reconstruction

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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.