髓鞘少突胶质细胞糖蛋白抗体相关疾病表现为溴隐亭治疗的难治性发热:1例报告

Q4 Nursing Journal of Neurocritical Care Pub Date : 2023-06-27 DOI:10.18700/jnc.230020
Jin San Lee, Sukyoon Lee, Seong-il Oh
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引用次数: 0

摘要

背景:脱髓鞘事件表现为异常的体温调节反应是罕见的,但髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)难治性发热却很少报道。病例报告:一名56岁女性,四肢瘫伴肢端感觉异常。入院时,尽管给予大剂量退烧药,仍出现发热并持续2天。脑磁共振成像(MRI)显示高强度病变累及上脑干。根据临床特点及血清MOG抗体阳性诊断为MOGAD。口服溴隐亭(2.5 mg/d)后,发热缓慢控制数日。结论:本病例解释了MOGAD患者持续发热可能是一种不常见的表现。脑MRI显示的上脑干病变可被认为是位于导水管周围灰质前部的病变,该部位的病变可能是患者不明原因持续发热的原因。
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Myelin oligodendrocyte glycoprotein antibody-associated disease manifesting as intractable fever managed by bromocriptine: a case report
Background: Demyelinating events expressed as abnormal thermoregulatory responses are rare, but intractable fever in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is very rarely reported.Case Report: A 56-year-old woman presented with quadriparesis with acroparesthesia. During the admission, fever developed and persisted for 2 days despite the administration of high-dose antipyretics. Brain magnetic resonance imaging (MRI) showed hyperintense lesions involving the upper brainstem. A diagnosis of MOGAD was made according to the clinical characteristics and presence of seropositive MOG antibody. After administration of oral bromocriptine (2.5 mg/day), fever was slowly controlled for a few days.Conclusion: The present case explained that persistent fever in MOGAD could manifest as an uncommon manifestation. The lesion in the upper brainstem within the brain MRI could be thought of as a lesion anterior to the periaqueductal gray and the lesion at that site could be the cause of the patient's persistent fever with unknown origin.
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来源期刊
Journal of Neurocritical Care
Journal of Neurocritical Care Nursing-Advanced and Specialized Nursing
CiteScore
0.60
自引率
0.00%
发文量
16
审稿时长
10 weeks
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