[Peripheral neuropathy and myositis in idiopathic hypereosinophilic syndrome: case report]. / Neuropatia periférica e miosite na síndrome hipereosinofílica idiopática: relato de caso.
Arq Neuropsiquiatr
; 62(1): 150-3, 2004 Mar.
Article
em Pt
| MEDLINE
| ID: mdl-15122451
We describe a case of idiopathic hypereosinophilic syndrome manifested by an axonal sensory-motor polyneuropathy (ASMP) and signals of myositis. A 20 year old woman began with progressive gait impairment with drops and presented with subacute lower limb edema associated with paresthesis and cramps. She showed hypotonia in the lower limbs, absence of knee and ankle jerks, steppage gait, and decreased sensation on both legs. Examinations of stools were negative. Blood examination showed 7700 leukocytes with 24% (1848/mm(3)) eosinophils. Electrodiagnostic studies showed axonal lesion in sensory and motor nerves. Muscle biopsy showed type 2 muscle fibers atrophy with discrete inflammatory cells, predominantly lymphocytic in perivascular and interstitial locations. She was treated with prednisone and all the symptoms subsided after two months.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Síndrome Hipereosinofílica
/
Doenças do Sistema Nervoso Periférico
/
Miosite
Limite:
Adult
/
Female
/
Humans
Idioma:
Pt
Revista:
Arq Neuropsiquiatr
Ano de publicação:
2004
Tipo de documento:
Article
País de afiliação:
Brasil
País de publicação:
Alemanha