A Case of Acute Inflammatory Demyelinating Polyradiculoneuropathy in a Patient with Systemic Lupus Erythematosus
Journal of Rheumatic Diseases
;
: 143-146, 2014.
Article
Dans Coréen
| WPRIM
| ID: wpr-20892
ABSTRACT
Neuropsychiatric manifestations in patients with systemic lupus erythematosus are fairly common, with a prevalence of 37~95%. Among 19 neuropsychiatric manifestations, acute inflammatory demyelinating polyradiculoneuropathy (AIDP) is quite rare, and is characterized by progressive, symmetric muscle weakness accompanied by absent or depressed deep tendon reflexes. Generally, plasma exchange and intravenous immunoglobulin are the main treatment modalities. Here, we report a case of AIDP in a 29-year-old SLE patient, who was fully recovered with a treatment of high-dose glucocorticoid and immunosuppressive agents. Ours case suggests that AIDP should be treated differently in SLE patients to avoid disastrous results.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Échange plasmatique
/
Polyradiculoneuropathie
/
Réflexe d'étirement
/
Immunoglobulines
/
Système nerveux central
/
Prévalence
/
Faiblesse musculaire
/
Syndrome de Guillain-Barré
/
Immunosuppresseurs
/
Lupus érythémateux disséminé
Type d'étude:
Étude de prévalence
Limites du sujet:
Adulte
/
Humains
langue:
Coréen
Texte intégral:
Journal of Rheumatic Diseases
Année:
2014
Type:
Article
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