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发热性疾病后发生的纵向广泛横贯性脊髓炎1例罕见病例报告

A Rare Case of Longitudinally Extensive Transverse Myelitis Following Febrile Illness: A Case Report.

作者信息

Wettasinghe Indika, Puthra Shiran, Sugathapala Hemal A, Mendis Suresh

机构信息

Internal Medicine, Colombo South Teaching Hospital, Colombo, LKA.

出版信息

Cureus. 2024 Mar 17;16(3):e56316. doi: 10.7759/cureus.56316. eCollection 2024 Mar.

DOI:10.7759/cureus.56316
PMID:38629009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11020659/
Abstract

Longitudinally extensive transverse myelitis (LETM) is a rapidly progressing demyelinating disease affecting the spinal cord over three or more vertebral segments. Most causes are idiopathic, while others include infections, autoimmune causes, central nervous system demyelinating diseases, and post vaccination. Here, we report a 37-year-old male who presented with a fever for six days with no source of infection and complained of pain and weakness in the bilateral lower limbs eight hours after admission. Though the neurological examination of the lower limbs was normal at that time, reduced power was detected 16 hours later, with loss of proprioception and sensation of pain with a sensory level at T4 vertebrae. Then, the patient became unable to vocalize, and the chest X-ray showed an elevated left hemidiaphragm. Thirty hours after admission, the patient went into type 2 respiratory arrest and was intubated. The magnetic resonance imaging (MRI) showed a longitudinally extensive transverse myelitis extending from the C2 vertebrae to the conus medullaris. Febrile illness is common in the medical setting in Sri Lanka, but its association with LETM is unusual. Since LETM is very rare and is a rapidly progressive disease, a high degree of clinical suspicion is crucial for early diagnosis and the initiation of treatment. This case underscores the importance of early diagnosis, which would require timely MRI, and prompt treatment with intravenous (IV) glucocorticoids or plasma exchange to reduce morbidity and mortality.

摘要

长节段横贯性脊髓炎(LETM)是一种快速进展的脱髓鞘疾病,累及三个或更多椎体节段的脊髓。大多数病因不明,其他病因包括感染、自身免疫性病因、中枢神经系统脱髓鞘疾病和疫苗接种后。在此,我们报告一名37岁男性,发热6天,无感染源,入院8小时后诉双侧下肢疼痛和无力。尽管当时下肢神经系统检查正常,但16小时后发现肌力下降,本体感觉丧失,疼痛感觉减退,感觉平面位于T4椎体。随后,患者无法发声,胸部X线显示左半膈抬高。入院30小时后,患者出现2型呼吸骤停并插管。磁共振成像(MRI)显示长节段横贯性脊髓炎,从C2椎体延伸至脊髓圆锥。发热性疾病在斯里兰卡的医疗环境中很常见,但其与LETM的关联并不常见。由于LETM非常罕见且是一种快速进展的疾病,高度的临床怀疑对于早期诊断和治疗的启动至关重要。该病例强调了早期诊断的重要性,这需要及时进行MRI检查,并及时用静脉注射(IV)糖皮质激素或血浆置换进行治疗,以降低发病率和死亡率。

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