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Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia

Kimura, A. ; Yoshino, H. ; Yuasa, T.

Journal of the neurological sciences, 2005-04, Vol.231 (1), p.89-93 [Periódico revisado por pares]

Shannon: Elsevier B.V

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Título:
Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia
Autor: Kimura, A. ; Yoshino, H. ; Yuasa, T.
Assuntos: Action Potentials - drug effects ; Action Potentials - physiology ; Atopic myelitis ; Biological and medical sciences ; Chronic inflammatory demyelinating polyneuropathy (CIDP) ; Electric Stimulation ; Functional Laterality - physiology ; Glomerulonephritis ; Hand Strength - physiology ; Humans ; IgE ; Immunoglobulin E - blood ; Immunoglobulins, Intravenous - therapeutic use ; Intravenous immunoglobulin (IVIg) ; Job Syndrome - complications ; Job Syndrome - therapy ; Male ; Medical sciences ; Middle Aged ; Mite antigen ; Multifocal motor neuropathy (MMN) ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - physiopathology ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Nerve Block - methods ; Neural Conduction - drug effects ; Neural Conduction - physiology ; Neurology ; Peripheral Nerves - physiopathology ; Peripheral Nerves - radiation effects ; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - complications ; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - therapy
É parte de: Journal of the neurological sciences, 2005-04, Vol.231 (1), p.89-93
Notas: ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
Descrição: We herein report the case of a 46 year old man with chronic inflammatory demyelinating polyneuropathy (CIDP) with hyperIgEaemia. The patient presented with bilateral weakness, generalized hyporeflexia, and mild paresthesia of the fingers of both hands. Nerve conduction studies revealed multiple sites of motor conduction block in the absence of sensory abnormalities. Muscle strength increased, as did compound muscle action potential (CMAP) amplitude immediately after the intravenous infusion of immunoglobulin (IVIg). Serum IgE levels also fluctuated in parallel with his relapsing–remitting clinical course. We propose that pure motor CIDP may be immune mediated and suggest that IgE-mediated allergy may be one potential cause of this condition.
Editor: Shannon: Elsevier B.V
Idioma: Inglês

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Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia

Kimura, A. ; Yoshino, H. ; Yuasa, T.

Shannon: Elsevier B.V

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