In:
Case Reports in Neurology, S. Karger AG, Vol. 11, No. 1 ( 2019-1-24), p. 17-23
Kurzfassung:
A 12-year-old girl was admitted to the authors’ hospital due to muscle weakness, gait disturbance, dysarthria, dysphagia, and diplopia. She experienced prodromal fever 10 days before admission. On examination, deep tendon reflex was absent in the extremities, and nerve conduction velocity was decreased in the ulnar nerve. She was diagnosed with Guillain-Barré syndrome (GBS). Despite steroid pulse therapy following administration of intravenous high-dose γ-globulin, clinical manifestations remained unchanged. Therefore, plasma exchange was performed on day 10 of the illness. The titer of serum 〈 i 〉 Mycoplasma 〈 /i 〉 immunoglobulin M level was increased. Immunological testing was positive for serum anti-galactocerebroside C antibody. On day 18 of the illness, however, she developed generalized convulsion. Brain magnetic resonance imaging revealed high intensity in the medial temporal lobes, including the hippocampus and thalamus on T2-weighted intensity imaging, which was consistent with limbic encephalitis. Further immunological tests revealed positivity for anti-N-methyl-D-aspartate-type glutamate receptor antibody in the cerebrospinal fluid. She was treated with additional plasma exchange; however, she exhibited residual manifestations including short-term memory disorder, emotional incontinence, and convulsions. This article describes a notable case of limbic encephalitis following GBS associated with prodromal 〈 i 〉 Mycoplasma 〈 /i 〉 infection. It is interesting that autoimmune encephalopathy is concomitant with autoimmune polyneuropathy subsequent to 〈 i 〉 Mycoplasma 〈 /i 〉 infection.
Materialart:
Online-Ressource
ISSN:
1662-680X
Sprache:
Englisch
Verlag:
S. Karger AG
Publikationsdatum:
2019
ZDB Id:
2505302-4
