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Electroconvulsive therapy for catatonia in juvenile neuropsychiatric lupus.

Authors :
Leon, T
Aguirre, A
Pesce, C
Sanhueza, P
Toro, P
Source :
Lupus; Sep2014, Vol. 23 Issue 10, p1066-1068, 3p, 1 Graph
Publication Year :
2014

Abstract

Neuropsychiatric manifestations are serious and frequent complications of systemic lupus erythematous (SLE). Catatonia is a neuropsychiatric disorder characterized by motor disturbance (including waxy flexibility and catalepsy), stupor, excitement, negativism, mutism, echopraxia and echolalia. Catatonia associated with SLE has been only rarely reported, especially in children. Here we present a case of a 14-year-old patient encountered in consultation-liaison psychiatry who presented catatonia associated with SLE. Her catatonia was refractory to treatment with pulse methylprednisolone, intravenous cyclophosphamide and rituximab. The patient responded to a combined therapy of electroconvulsive therapy and benzodiazepines. The present case suggests that although rarely reported, catatonia seen in the background of SLE should be promptly identified and treated to reduce the morbidity. [ABSTRACT FROM PUBLISHER]

Details

Language :
English
ISSN :
09612033
Volume :
23
Issue :
10
Database :
Complementary Index
Journal :
Lupus
Publication Type :
Academic Journal
Accession number :
97895251
Full Text :
https://doi.org/10.1177/0961203314533603