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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 저널정보
- 대한자기공명의과학회 Investigative Magnetic Resonance Imaging Investigative Magnetic Resonance Imaging 제25권 제3호
- 발행연도
- 2021.9
- 수록면
- 189 - 192 (4page)
이용수
초록· 키워드
오류제보하기
Anti-myelin oligodendrocyte glycoprotein (anti-MOG) syndrome is an immune mediated inflammatory condition of the central nervous system, which usually involves spinal cord and optic nerves. Herein, we studied the case of a 57-year old female patient who presented with acute/subacute symptoms of sphincter dysfunction, paraparesis, and ocular pain. The patient was diagnosed with anti-MOG syndrome with findings resembling snake-eye appearance (SEA), characterized by nearly symmetrical round high signal intensity lesions located at anterior horns (gray matter) on T2-weighted image.
목차
등록된 정보가 없습니다.
참고문헌 (10)
참고문헌 신청
Zhang Z / 2014 / Is the"snake-eye"MRI sign correlated to anterior spinal artery occlusion on CT angiography in cervical spondylotic myelopathy and amyotrophy / Eur Spine J 23:1541~1547
Zalewski NL / 2019 / Characteristics of spontaneous spinal cord infarction and proposed diagnostic criteria / JAMA Neurol 76:56~63
Lana-Peixoto MA / 2019 / Neuromyelitisoptica spectrum disorder and anti-MOG syndromes / Biomedicines 7:42
Deneve M / 2019 / MRI features of demyelinating disease associated with anti-MOG antibodies in adults / J Neuroradiol 46:312~318
Shor N / MRI characteristics of MOG-Ab associated disease in adults : an update / Rev Neurol(Paris)2021; 177:39~50
Zalewski NL / 2019 / Characteristics of spontaneous spinal cord infarction and proposed diagnostic criteria / JAMA Neurol 76:56~63
Lana-Peixoto MA / 2019 / Neuromyelitisoptica spectrum disorder and anti-MOG syndromes / Biomedicines 7:42
Deneve M / 2019 / MRI features of demyelinating disease associated with anti-MOG antibodies in adults / J Neuroradiol 46:312~318
Shor N / MRI characteristics of MOG-Ab associated disease in adults : an update / Rev Neurol(Paris)2021; 177:39~50
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