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Solitary subdural osteomas: Systematic review of the literature with an illustrative case

BACKGROUND: Subdural osteomas represent an extremely rare entity with only 20 cases described to date. Despite the typical benign behavior, these tumors can grow to compress the brain and occasionally detach from the dura mater. METHODS: A systematic search of the literature was performed in complia...

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Autores principales: Colamaria, Antonio, Sacco, Matteo, Iodice, Savino, Settembrini, Giulia, Ciavarella, Giuseppe, Fochi, Nicola Pio, Carbone, Francesco, Leone, Augusto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168329/
https://www.ncbi.nlm.nih.gov/pubmed/35673651
http://dx.doi.org/10.25259/SNI_245_2022
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author Colamaria, Antonio
Sacco, Matteo
Iodice, Savino
Settembrini, Giulia
Ciavarella, Giuseppe
Fochi, Nicola Pio
Carbone, Francesco
Leone, Augusto
author_facet Colamaria, Antonio
Sacco, Matteo
Iodice, Savino
Settembrini, Giulia
Ciavarella, Giuseppe
Fochi, Nicola Pio
Carbone, Francesco
Leone, Augusto
author_sort Colamaria, Antonio
collection PubMed
description BACKGROUND: Subdural osteomas represent an extremely rare entity with only 20 cases described to date. Despite the typical benign behavior, these tumors can grow to compress the brain and occasionally detach from the dura mater. METHODS: A systematic search of the literature was performed in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. After screening for duplicates, 179 publications met the eligibility criteria. Finally, 18 manuscripts were included in this review. Moreover, a detailed description of an illustrative case is provided. RESULTS: The median age at diagnosis was 43.2 years, showing a female prevalence. The inner table of the frontal bone was reported as the most frequent location, and in six cases, the lesions did not show any relation with the dura, which appeared intact. Surgical resection appears to be an effective and safe management option. In the present work, the case of a 60-year-old female who presented with persistent, diffuse headaches which had first occurred 6 months earlier is described. On admission, the physical and neurological examinations were unremarkable, and her medical history disclosed no systemic disease, meningitis, or head injury. Computed tomography showed a homogeneous, high-density nodule attached to the inner table of the left middle cranial fossa. CONCLUSION: In addition to an in-depth case description, the first systematic and qualitative review of the literature on intracranial subdural osteomas using the PRISMA is provided.
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spelling pubmed-91683292022-06-06 Solitary subdural osteomas: Systematic review of the literature with an illustrative case Colamaria, Antonio Sacco, Matteo Iodice, Savino Settembrini, Giulia Ciavarella, Giuseppe Fochi, Nicola Pio Carbone, Francesco Leone, Augusto Surg Neurol Int Review Article BACKGROUND: Subdural osteomas represent an extremely rare entity with only 20 cases described to date. Despite the typical benign behavior, these tumors can grow to compress the brain and occasionally detach from the dura mater. METHODS: A systematic search of the literature was performed in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. After screening for duplicates, 179 publications met the eligibility criteria. Finally, 18 manuscripts were included in this review. Moreover, a detailed description of an illustrative case is provided. RESULTS: The median age at diagnosis was 43.2 years, showing a female prevalence. The inner table of the frontal bone was reported as the most frequent location, and in six cases, the lesions did not show any relation with the dura, which appeared intact. Surgical resection appears to be an effective and safe management option. In the present work, the case of a 60-year-old female who presented with persistent, diffuse headaches which had first occurred 6 months earlier is described. On admission, the physical and neurological examinations were unremarkable, and her medical history disclosed no systemic disease, meningitis, or head injury. Computed tomography showed a homogeneous, high-density nodule attached to the inner table of the left middle cranial fossa. CONCLUSION: In addition to an in-depth case description, the first systematic and qualitative review of the literature on intracranial subdural osteomas using the PRISMA is provided. Scientific Scholar 2022-05-13 /pmc/articles/PMC9168329/ /pubmed/35673651 http://dx.doi.org/10.25259/SNI_245_2022 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Review Article
Colamaria, Antonio
Sacco, Matteo
Iodice, Savino
Settembrini, Giulia
Ciavarella, Giuseppe
Fochi, Nicola Pio
Carbone, Francesco
Leone, Augusto
Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title_full Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title_fullStr Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title_full_unstemmed Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title_short Solitary subdural osteomas: Systematic review of the literature with an illustrative case
title_sort solitary subdural osteomas: systematic review of the literature with an illustrative case
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168329/
https://www.ncbi.nlm.nih.gov/pubmed/35673651
http://dx.doi.org/10.25259/SNI_245_2022
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