Childhood sclerodermatomyositis with generalized morphea.
Indian J Dermatol Venereol Leprol
;
2008 Mar-Apr; 74(2): 148-50
Artículo
en Inglés
| IMSEAR
| ID: sea-52625
ABSTRACT
Systemic sclerosis (SS) and dermatomyositis (DM) are both multisystem disorders and share some common clinical features. We report here an 11 year-old girl whose disease showed a changing clinical pattern from juvenile systemic sclerosis (JSS) to slowly progressing juvenile dermatomyositis (JDM) and had associated generalized morphea. Serological studies revealed antinuclear antibodies (ANA) with a speckled pattern. Topoisomerase-I (Scl-70), U1 RNP (ribonucleoprotein), anti-Ro, anti-La and anti Jo-1 antibody tests were negative. Electromyography (EMG) was suggestive of primary muscle disease and histopathological findings indicated scleroderma. The patient fulfilled the American College Rheumatology (ACR) diagnostic criteria for JSS as well as Bohan and Peter criteria for JDM separately and hence, was diagnosed to have sclerodermatomyositis (SDM). Mixed connective tissue disease (MCTD) and antisynthetase antibody syndrome (ASS) which share same clinical features with SS and DM were excluded by immunological studies.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Esclerodermia Localizada
/
Esclerodermia Sistémica
/
Femenino
/
Humanos
/
Niño
/
Dermatomiositis
Idioma:
Inglés
Revista:
Indian J Dermatol Venereol Leprol
Año:
2008
Tipo del documento:
Artículo
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