ArticleLife (Basel, Switzerland)2022
Primary Intraosseous Osteolytic Meningioma with Aggressive Clinical Behaviour: Clinico-Pathologic Correlation and Proposed New Clinical Classification.
Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed, 10 citations in OpenAlex.
- Operative diagnosis of a meningioma-like intraosseous skull lesion revealing multiple myeloma: Case report and literature review.Surgical neurology international · 2026Article
- Deciphering extracranial metastasis in high-grade meningiomas: insights from a case study and literature review.Annals of medicine and surgery (2012) · 2025Article
- Primary intraosseous meningioma: a case of early symptomatic calvarial origin meningioma.Journal of surgical case reports · 2024Article
- Scalp metastasis from atypical meningioma: A case report and literature review.Clinical case reports · 2024Article
- Review
- Cystic meningiomas: A complex diagnostic challenge and clinicopathological insights from a unique case presentation.Clinical case reports · 2024Article
- Primary intraosseous meningioma with subcutaneous and dural invasion: A case report and literature review.Frontiers in surgery · 2022Article
- Diagnostic Imaging of Primary Cutaneous Osteoma of the Forehead.Case reports in dermatologyArticle
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Authors and funding
8 authors at 6 institutions in 4 countries.
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No grant is acknowledged in the PubMed record.
Abstract
(1) Introduction: Primary intraosseous osteolytic meningiomas (PIOM) are non-dural-based tumors predominantly presenting an osteolytic component with or without hyperostotic reactions. They are a subset of primary extradural meningiomas (PEM). In this study, we present a peculiar case with a systematic literature review and propose a new classification considering the limitations of previous classification systems. (2) Materials and Methods: Using a systematic search protocol in Google Scholar, PubMed, and Scopus databases, we extracted all case studies on PIOM published from inception to December 2020. A 46-year-old female patient form Dhaka, Bangladesh, was also described. The search protocol was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. (3) Results: Here, we present a 46-year-old female patient with PIOM who successfully underwent bifrontal craniotomy and gross total removal (GTR) of the tumor. At 6-month follow-up, no tumor recurrence was shown. Including our new case, 55 total cases from 47 articles were included in the analysis. PIOMs were in closer frequency among males (56.4%) and females (43.6%). The most common tumor location was the frontal and parietal calvarium, most commonly in the frontal bone (29.1%). Surgical resection was the predominant modality of treatment (87.3%); only 1.8% of patients were treated with radiotherapy, and 5.4% received a combination of surgery and radiotherapy. Gross total resection (GTR) was achieved in 80% of cases. Extracranial extension was reported in 41.8% of cases, dural invasion in 47.3%, and recurrence in 7.3%. Whole-body 68 Ga-DOTATOC PET/CT has also been reported as a useful tool both for differential diagnosis, radiotherapy contouring, and follow-up. Current treatments such as hydroxyurea and bevacizumab have variable success rates. We have also suggested a new classification which would provide a simple common ground for further research in this field. (4) Conclusions: Surgical resection, especially GTR, is the treatment of choice for PIOM, with a high GTR rate and low risk of complications and mortality. More research is needed on the differential diagnosis and specific treatment of PIOM.
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