IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent
{"title":"原发性硬脑膜淋巴瘤：病例报告","authors":"IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent","doi":"10.1016/j.inat.2024.101965","DOIUrl":null,"url":null,"abstract":"<div><h3>Backgroung</h3><p>Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.</p></div><div><h3>Case presentation</h3><p>A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.</p></div><div><h3>Conclusion</h3><p>Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101965"},"PeriodicalIF":0.4000,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000112/pdfft?md5=f0e22b56e4de419238736ca64f116743&pid=1-s2.0-S2214751924000112-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Primary dural Lymphoma: A case report\",\"authors\":\"IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent\",\"doi\":\"10.1016/j.inat.2024.101965\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Backgroung</h3><p>Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.</p></div><div><h3>Case presentation</h3><p>A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.</p></div><div><h3>Conclusion</h3><p>Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.</p></div>\",\"PeriodicalId\":38138,\"journal\":{\"name\":\"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management\",\"volume\":\"36 \",\"pages\":\"Article 101965\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2024-01-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2214751924000112/pdfft?md5=f0e22b56e4de419238736ca64f116743&pid=1-s2.0-S2214751924000112-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/S2214751924000112\",\"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/S2214751924000112","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.
Case presentation
A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.
Conclusion
Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.
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