Franz Jooji Onishi , Ana Camila Gandolfi , Rafi Felicio B. Dauar
{"title":"原发性颅骨肿瘤的鉴别诊断 - 单纯骨内硬膜外脑膜瘤的特征。病例报告和文献综述","authors":"Franz Jooji Onishi , Ana Camila Gandolfi , Rafi Felicio B. Dauar","doi":"10.1016/j.inat.2023.101940","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>This case report aims to describe a rare occurrence of a purely intraosseous meningioma, presenting as a lytic bone lesion in the skull.</p></div><div><h3>Case Report</h3><p>We present the case of a 67-year-old female patient who presented with a persistent headache and underwent diagnostic imaging, including CT scan and MRI. Surgical resection with wide margins and cranial reconstruction was performed, followed by histopathological examination of the tumor.</p></div><div><h3>Discussion</h3><p>The radiological investigation revealed an infiltrative and lytic heterogeneous lesion in the left parietal bone. Whole-body PET-CT scan showed no signs of primary involvement. The patient underwent successful surgery, and the histopathological examination confirmed the diagnosis of a grade I meningothelial meningioma with adjacent hyperostosis. Primary intraosseous meningiomas are exceedingly rare and challenging to diagnose due to their mimicry of other benign and malignant skull lesions. Surgical resection with wide margins is recommended, and histopathological examination with immunohistochemistry aids in confirming the diagnosis. Long-term surveillance is necessary due to the potential for recurrence and malignant transformation.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101940"},"PeriodicalIF":0.4000,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751923002232/pdfft?md5=687e941976747e63d48f030672543232&pid=1-s2.0-S2214751923002232-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Differential diagnosis of a primary skull bone tumor – Characteristics of an purely intraosseous extradural meningioma. Case report and literature review\",\"authors\":\"Franz Jooji Onishi , Ana Camila Gandolfi , Rafi Felicio B. Dauar\",\"doi\":\"10.1016/j.inat.2023.101940\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>This case report aims to describe a rare occurrence of a purely intraosseous meningioma, presenting as a lytic bone lesion in the skull.</p></div><div><h3>Case Report</h3><p>We present the case of a 67-year-old female patient who presented with a persistent headache and underwent diagnostic imaging, including CT scan and MRI. Surgical resection with wide margins and cranial reconstruction was performed, followed by histopathological examination of the tumor.</p></div><div><h3>Discussion</h3><p>The radiological investigation revealed an infiltrative and lytic heterogeneous lesion in the left parietal bone. Whole-body PET-CT scan showed no signs of primary involvement. The patient underwent successful surgery, and the histopathological examination confirmed the diagnosis of a grade I meningothelial meningioma with adjacent hyperostosis. Primary intraosseous meningiomas are exceedingly rare and challenging to diagnose due to their mimicry of other benign and malignant skull lesions. Surgical resection with wide margins is recommended, and histopathological examination with immunohistochemistry aids in confirming the diagnosis. Long-term surveillance is necessary due to the potential for recurrence and malignant transformation.</p></div>\",\"PeriodicalId\":38138,\"journal\":{\"name\":\"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management\",\"volume\":\"36 \",\"pages\":\"Article 101940\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2023-12-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2214751923002232/pdfft?md5=687e941976747e63d48f030672543232&pid=1-s2.0-S2214751923002232-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214751923002232\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214751923002232","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Differential diagnosis of a primary skull bone tumor – Characteristics of an purely intraosseous extradural meningioma. Case report and literature review
Objective
This case report aims to describe a rare occurrence of a purely intraosseous meningioma, presenting as a lytic bone lesion in the skull.
Case Report
We present the case of a 67-year-old female patient who presented with a persistent headache and underwent diagnostic imaging, including CT scan and MRI. Surgical resection with wide margins and cranial reconstruction was performed, followed by histopathological examination of the tumor.
Discussion
The radiological investigation revealed an infiltrative and lytic heterogeneous lesion in the left parietal bone. Whole-body PET-CT scan showed no signs of primary involvement. The patient underwent successful surgery, and the histopathological examination confirmed the diagnosis of a grade I meningothelial meningioma with adjacent hyperostosis. Primary intraosseous meningiomas are exceedingly rare and challenging to diagnose due to their mimicry of other benign and malignant skull lesions. Surgical resection with wide margins is recommended, and histopathological examination with immunohistochemistry aids in confirming the diagnosis. Long-term surveillance is necessary due to the potential for recurrence and malignant transformation.