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1. 多源性心房性頻拍 multifocal atrial tachycardia
2. 多巣性運動ニューロパチー multifocal motor neuropathy
3. 進行性多巣性白質脳症：疫学、臨床症状、および診断 progressive multifocal leukoencephalopathy epidemiology clinical manifestations and diagnosis
4. 進行性多巣性白質脳症：治療および予後 progressive multifocal leukoencephalopathy treatment and prognosis
5. JCポリオーマウイルス、BKポリオーマウイルスおよびその他のヒトポリオーマウイルスのウイルス学、疫学および病因 virology epidemiology and pathogenesis of jc polyomavirus bk polyomavirus and other human polyomaviruses

Japanese Journal

リンク元	「多巣的」
拡張検索	「持続性伝導ブロックを伴う多巣性脱髄性ニューロパチー」「多巣性脈絡膜炎」「多巣性運動ニューロパシー」「多巣性運動神経障害」

1982年にLewis, Sumnerが報告。ALSとの鑑別を要する病態。抗GM1-IgM抗体が上昇することがある。治療では大量ガンマグロブリン静注が奏効するものがある。

Lewis RA, Sumner AJ, Brown MJ, Asbury AK.AbstractWe describe five patients with a chronic asymmetric sensorimotor neuropathy most pronounced in the upper extremities with focal involvement of individual nerves. Diagnosis was established by electrophysiologic evidence of persistent multifocal conduction block. Sural nerve biopsy in three patients showed primarily demyelinating-remyelinating changes with varying degrees of fiber loss. Two patients had acute optic neuritis, indicating that the disorder was not always restricted to the peripheral nervous system. Two patients treated with corticosteroids improved, whereas three untreated patients had static deficits or steady progression of symptoms. Chronic multifocal demyelinating neuropathy with persistent conduction block seems to be a variant of chronic acquired demyelinating polyneuropathy and may be immunologically mediated.
Neurology.Neurology.1982 Sep;32(9):958-64.
We describe five patients with a chronic asymmetric sensorimotor neuropathy most pronounced in the upper extremities with focal involvement of individual nerves. Diagnosis was established by electrophysiologic evidence of persistent multifocal conduction block. Sural nerve biopsy in three patients s
PMID 7202168