{"title":"纤维软骨栓塞性脊髓梗死,误诊为胶质纤维酸性蛋白自身免疫性横脊髓炎1例","authors":"Felix E Chukwudelunzu, Timothy Young","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Fibrocartilaginous embolism causing spinal cord infarct is rare, and a high index of clinical suspicion is needed for accurate diagnosis.</p><p><strong>Case presentation: </strong>A 65-year-old woman presented to our hospital with back pain, paraparesis, and neurogenic bladder. Magnetic resonance imaging showed a T4-T7 signal abnormality that was misdiagnosed initially and treated as autoimmune myelitis.</p><p><strong>Discussion: </strong>Fibrocartilaginous spinal cord infarction is rare and remains a clinical diagnosis with supportive imaging findings. The imaging findings may be nonspecific, and other etiologic diagnostic considerations must be excluded.</p><p><strong>Conclusion: </strong>Fibrocartilaginous embolism causing spinal cord infarct can be mistaken for transverse myelitis. A high index of clinical suspicion with clinical and radiologic correlation is necessary to make accurate diagnosis and avoid unnecessary treatment.</p>","PeriodicalId":94268,"journal":{"name":"WMJ : official publication of the State Medical Society of Wisconsin","volume":"124 1","pages":"63-66"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fibrocartilaginous Embolism Spinal Cord Infarction, Mistaken for Glial Fibrillary Acidic Protein Autoimmune Transverse Myelitis: A Case Report.\",\"authors\":\"Felix E Chukwudelunzu, Timothy Young\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Fibrocartilaginous embolism causing spinal cord infarct is rare, and a high index of clinical suspicion is needed for accurate diagnosis.</p><p><strong>Case presentation: </strong>A 65-year-old woman presented to our hospital with back pain, paraparesis, and neurogenic bladder. Magnetic resonance imaging showed a T4-T7 signal abnormality that was misdiagnosed initially and treated as autoimmune myelitis.</p><p><strong>Discussion: </strong>Fibrocartilaginous spinal cord infarction is rare and remains a clinical diagnosis with supportive imaging findings. The imaging findings may be nonspecific, and other etiologic diagnostic considerations must be excluded.</p><p><strong>Conclusion: </strong>Fibrocartilaginous embolism causing spinal cord infarct can be mistaken for transverse myelitis. A high index of clinical suspicion with clinical and radiologic correlation is necessary to make accurate diagnosis and avoid unnecessary treatment.</p>\",\"PeriodicalId\":94268,\"journal\":{\"name\":\"WMJ : official publication of the State Medical Society of Wisconsin\",\"volume\":\"124 1\",\"pages\":\"63-66\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"WMJ : official publication of the State Medical Society of Wisconsin\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"WMJ : official publication of the State Medical Society of Wisconsin","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fibrocartilaginous Embolism Spinal Cord Infarction, Mistaken for Glial Fibrillary Acidic Protein Autoimmune Transverse Myelitis: A Case Report.
Introduction: Fibrocartilaginous embolism causing spinal cord infarct is rare, and a high index of clinical suspicion is needed for accurate diagnosis.
Case presentation: A 65-year-old woman presented to our hospital with back pain, paraparesis, and neurogenic bladder. Magnetic resonance imaging showed a T4-T7 signal abnormality that was misdiagnosed initially and treated as autoimmune myelitis.
Discussion: Fibrocartilaginous spinal cord infarction is rare and remains a clinical diagnosis with supportive imaging findings. The imaging findings may be nonspecific, and other etiologic diagnostic considerations must be excluded.
Conclusion: Fibrocartilaginous embolism causing spinal cord infarct can be mistaken for transverse myelitis. A high index of clinical suspicion with clinical and radiologic correlation is necessary to make accurate diagnosis and avoid unnecessary treatment.