{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T04:03:04Z","timestamp":1787025784531,"version":"build-2736575974"},"reference-count":72,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"20","license":[{"start":{"date-parts":[[2025,5,19]],"date-time":"2025-05-19T00:00:00Z","timestamp":1747612800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Cosmet Laser Ther"],"published-print":{"date-parts":[[2025,5,19]]},"abstract":"<jats:sec>\n                    <jats:title>BACKGROUND<\/jats:title>\n                    <jats:p>Meningiomas are the most common benign tumors among CNS neoplasms. In the pediatric population, however, they account for only 0.4%\u20134.6% of all intracranial neoplasms; they are rare inside the brain parenchyma and are frequently confused with other entities, such as glioneuronal tumors and cavernomas, among others.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>OBSERVATIONS<\/jats:title>\n                    <jats:p>The authors describe the case of a 4-year-old male who presented to the emergency department for evaluation of periorbital cellulitis and was incidentally diagnosed with a brain tumor. MRI demonstrated an expansive heterogeneous lesion, 2.2 \u00d7 1.9 \u00d7 1.8 cm, in the left lingual gyrus. Spectroscopy and perfusion imaging suggested a low-grade glioneuronal tumor. After thorough discussion, the family and medical team elected to pursue surgical treatment. The patient had an uneventful postoperative recovery, and subsequent pathological and immunohistochemical analysis confirmed the diagnosis of a fibrous meningioma (WHO grade 1).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>LESSONS<\/jats:title>\n                    <jats:p>Intraparenchymal meningiomas are a rare and misdiagnosed tumor, especially in the pediatric age group, and therefore are not usually considered in the differential diagnosis of intra-axial neoplasms in children. When suspected, surgery may be encouraged due to the tendency of these tumors to exhibit more aggressive behavior compared with adult meningiomas.<\/jats:p>\n                    <jats:p>\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/thejns.org\/doi\/10.3171\/CASE24611\">https:\/\/thejns.org\/doi\/10.3171\/CASE24611<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3171\/case24611","type":"journal-article","created":{"date-parts":[[2025,5,20]],"date-time":"2025-05-20T06:41:58Z","timestamp":1747723318000},"source":"Crossref","is-referenced-by-count":1,"title":["Incidental pediatric intraparenchymal meningioma: illustrative case"],"prefix":"10.3171","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0009-0007-8952-9662","authenticated-orcid":true,"given":"Adriano M.","family":"Lino-Filho","sequence":"first","affiliation":[{"name":"Division of Neurosurgery, Department of Surgery, Clinics Hospital, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B\u00e1rbara A.","family":"Morais","sequence":"additional","affiliation":[{"name":"Division of Neurosurgery, Department of Surgery, Clinics Hospital, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"},{"name":"Department of Neurological Surgery, Children\u2019s Hospital, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4342-5506","authenticated-orcid":true,"given":"Mateus Neves Faria","family":"Fernandes","sequence":"additional","affiliation":[{"name":"School of Medicine, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jairo Porfirio","family":"Oliveira-Junior","sequence":"additional","affiliation":[{"name":"Division of Neurosurgery, Department of Surgery, Clinics Hospital, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-5950-2651","authenticated-orcid":true,"given":"Bruna","family":"Estrozi","sequence":"additional","affiliation":[{"name":"Department of Pathology, Clinics Hospital, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4003-5294","authenticated-orcid":true,"given":"Weder Silva","family":"Borges-Junior","sequence":"additional","affiliation":[{"name":"School of Medicine, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0114-0278","authenticated-orcid":true,"given":"Paulo Ronaldo J.","family":"Ribeiro","sequence":"additional","affiliation":[{"name":"Division of Neurosurgery, Department of Surgery, Clinics Hospital, Federal University of Goi\u00e1s, Goi\u00e2nia, Goi\u00e1s, Brazil"},{"name":"Department of Neurological Surgery, Children\u2019s Hospital, Goi\u00e2nia, Goi\u00e1s, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1754","reference":[{"issue":"1","key":"bib1","series-title":"Eur J Med Res","first-page":"39","article-title":"The global prevalence of primary central nervous system tumors: a systematic review and meta-analysis","volume":"28","author":"Salari","year":"2023","unstructured":"Salari NGhasemi HFatahian RThe global prevalence of primary central nervous system tumors: a systematic review and meta-analysis. 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J Neurosurg Pediatr. 2017;20(2):141-148."},{"issue":"5","key":"bib4","series-title":"World J Radiol","first-page":"188","article-title":"A review on dural tail sign","volume":"2","author":"Sotoudeh","year":"2010","unstructured":"Sotoudeh HYazdi HR.A review on dural tail sign. World J Radiol. 2010;2(5):188-192."},{"issue":"6","key":"bib5","series-title":"J Neurosurg","first-page":"489","article-title":"Central nervous system meningiomas in the first two decades of life: a clinicopathological analysis of 87 patients","volume":"103","author":"Rushing","year":"2005","unstructured":"Rushing EJOlsen CMena HCentral nervous system meningiomas in the first two decades of life: a clinicopathological analysis of 87 patients. 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J Neuroradiol. 2012;39(4):218-226."},{"issue":"1","key":"bib25","series-title":"JBR-BTR","first-page":"46","article-title":"Intraparenchymal meningioma in a child","volume":"97","author":"Werbrouck","year":"2014","unstructured":"Werbrouck CFlorin DVan Holsbeeck BLaridon EDe Weweire MMarrannes J.Intraparenchymal meningioma in a child. JBR-BTR. 2014;97(1):46."},{"issue":"12","key":"bib26","series-title":"Childs Nerv Syst","first-page":"2151","article-title":"Intracerebral cystic rhabdoid papillary meningioma in an 11-year-old patient","volume":"30","author":"Jia","year":"2014","unstructured":"Jia WSonoda YSaito REndo TWatanabe MTominaga T.Intracerebral cystic rhabdoid papillary meningioma in an 11-year-old patient. 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