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1.
eNeurologicalSci ; 27: 100395, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35295746

ABSTRACT

We report a 77-year-old woman with a thymoma, anti-LGI1antibody associated encephalitis (LGI1 encephalitis), and MG accompanied by positive anti-acetylcholine receptor antibodies (AchR Ab) and anti-titin antibodies (titin Ab). She was treated with thymomectomy followed by immunosuppressive therapy, which resulted in immediate amelioration of motor weakness and gradual improvement of cognitive impairment over the next two years. LGI1 Ab were positive at two months after thymomectomy, followed by negative conversion demonstrated on 1 year examination. The AchR Ab level had gradually decreased but titin Ab was positive on re-examination after two years, although the cognition and motor impairment symptoms had been alleviated. In patients with suspected autoimmune encephalitis, the detection of several autoantibodies including LGI1 and thymomas provides useful information for making an accurate diagnosis.

2.
Brain Nerve ; 68(5): 567-71, 2016 May.
Article in Japanese | MEDLINE | ID: mdl-27156510

ABSTRACT

A 52-year-old woman developed abnormal behavior and disturbance of consciousness subsequent to several days with a cold. On admission, she was very confused, with incoherent speech, and an inability to recognize family faces. Diffusion weighted MRI showed high intensity signal change in the bilateral medial temporal lobes, including the hippocampus. Cerebrospinal fluid examination was normal. Tests including various viral antibody titers provided no evidence of infection. Several neuronal antibodies including anti-VGKC and -NMDA receptor antibody were absent. Evidence of malignancy was not apparent. She was diagnosed with acute limbic encephalitis complicated by Sjögren's syndrome (SjS), due to the fact that she had a past history of SjS, elevation of anti-SS-A antibody, pleuritis and pericarditis. Her symptoms gradually improved after administration of steroids including pulse therapy; however, her amnesia remained for a long time. In diagnosing acute limbic encephalitis, we should consider SjS as an underlying disease, even though it is rare.


Subject(s)
Limbic Encephalitis/etiology , Sjogren's Syndrome/complications , Acute Disease , Female , Hippocampus/pathology , Humans , Limbic Encephalitis/diagnosis , Limbic Encephalitis/drug therapy , Limbic Encephalitis/pathology , Magnetic Resonance Imaging , Middle Aged , Sjogren's Syndrome/drug therapy , Sjogren's Syndrome/pathology , Temporal Lobe/pathology
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