ArticleWorld journal of clinical cases2020
Anti-N-methyl-D-aspartate-receptor antibody encephalitis combined with syphilis: A case report.
Article in World journal of clinical cases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.
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Who cites it
5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.
- The spectrum of movement disorders in neurosyphilis: A systematic review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Pooled it
- Neurosyphilis complicated by anti-γ-aminobutyric acid-B receptor encephalitis: A case report.World journal of clinical cases · 2024Article
- Neurosyphilis with positive anti-N-methyl-D-aspartate receptor antibody: a case report.Frontiers in neurology · 2023Article
- Secondary immunoreaction in patients with neurosyphilis and its relevance to clinical outcomes.Frontiers in neurology · 2023Article
- Neurosyphilis and limbic encephalitis: practical guidance for diagnosis and treatment sequencing at an infection-autoimmunity interface.Frontiers in neurologyArticle
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
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Abstract
backgroundAnti-N-methyl-D-aspartate-receptor (NMDAR) encephalitis is a common type of autoimmune encephalitis characterized by complex clinical signs and variable imaging manifestations. The pathogenesis of the disease is unclear. Syphilis is an infectious disease caused by CASE SUMMARY: A 32-year-old man was admitted to our hospital with complaints of cognitive decline, diplopia, and walking instability during the previous 6 mo. He developed dysarthria, difficulty swallowing, and involuntary shaking of his head, neck, and limbs during the month prior to presentation. Cranial magnetic resonance imaging showed symmetrical abnormal signals in the pons, midbrain, and bilateral basal ganglia, and inflammatory demyelination was considered. The diagnosis of syphilis was confirmed based on the syphilis diagnosis test and the syphilis rapid test. He was given anti-syphilis treatment, but the above symptoms gradually worsened. Anti-NMDAR antibody was positive in cerebrospinal fluid but was negative in serum. Due to the cerebrospinal fluid findings, anti-NMDAR encephalitis was a consideration. According to the patient's weight, he was treated with intravenous methylprednisolone 1 g QD for 5 d, with the dose gradually decreased for 6 mo, and immunoglobulin 25 g QD for 5 d; his symptoms improved after treatment.
conclusionThis case shows that anti-NMDAR encephalitis may be combined with syphilis, which should be recognized to avoid misdiagnosis and treatment delay.
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