{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,4]],"date-time":"2025-10-04T17:47:41Z","timestamp":1759600061956,"version":"3.37.3"},"reference-count":48,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2014,4,7]],"date-time":"2014-04-07T00:00:00Z","timestamp":1396828800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neuropathology"],"published-print":{"date-parts":[[2014,10]]},"abstract":"<jats:p>Meningiomas are the most common primary intracranial tumors. They are usually benign and slowly growing; however, they may show histologically malignant features categorizing them into grade <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">III<\/jats:styled-content> of <jats:styled-content style=\"fixed-case\">W<\/jats:styled-content>orld <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>ealth <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>rganization (<jats:styled-content style=\"fixed-case\">WHO<\/jats:styled-content>) classification. Rhabdoid meningioma (<jats:styled-content style=\"fixed-case\">RM<\/jats:styled-content>) is an uncommon meningioma variant categorized as <jats:styled-content style=\"fixed-case\">WHO<\/jats:styled-content> grade <jats:styled-content style=\"fixed-case\">III<\/jats:styled-content>. The clinical course of <jats:styled-content style=\"fixed-case\">RM<\/jats:styled-content> is determined by local recurrences, invasion of adjacent brain and\/or dura, widespread leptomeningeal dissemination, remote metastases and fatal clinical outcome. Herein we report a case with recurrent aggressive left occipital parasagittal region <jats:styled-content style=\"fixed-case\">RM<\/jats:styled-content> in which the patient initially declined radiation treatment. The tumor was resected four times in 5 years. Histopathological examination revealed a rhabdoid meningioma with metaplastic, papillary and chordoid differentiation. Six months after her fourth operation the patient died of progressive disease. <jats:styled-content style=\"fixed-case\">RM<\/jats:styled-content> is a rare subtype of malignant meningioma and the role of different adjuvant therapeutic options are still unknown. Clinical presentation, radiological features and pathologic findings of this uncommon tumor are discussed.<\/jats:p>","DOI":"10.1111\/neup.12122","type":"journal-article","created":{"date-parts":[[2014,4,7]],"date-time":"2014-04-07T08:11:56Z","timestamp":1396858316000},"page":"475-483","source":"Crossref","is-referenced-by-count":7,"title":["Aggressive rhabdoid meningioma with osseous, papillary and chordoma\u2010like appearance"],"prefix":"10.1111","volume":"34","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5558-0175","authenticated-orcid":false,"given":"Pinar","family":"Karabagli","sequence":"first","affiliation":[{"name":"Department of Pathology Faculty of Medicine Selcuk University  Konya Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hakan","family":"Karabagli","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery Faculty of Medicine Selcuk University  Konya Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Guler","family":"Yavas","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology Faculty of Medicine Selcuk University  Konya Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,4,7]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"164","volume-title":"WHO Classification of Tumours of the Central Nervous System","author":"Perry A","year":"2007"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jocn.2009.12.014"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF02479430"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-199802000-00012"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-199812000-00005"},{"key":"e_1_2_5_7_1","first-page":"176","volume-title":"WHO Classification of Tumours. 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