A Case of Spondyloepiphyseal Dysplasia Tarda (SEDT) Misdiagnosed as Ankylosing Spondylitis
Journal of Rheumatic Diseases
;
: 311-314, 2011.
Artigo
em Coreano
| WPRIM
| ID: wpr-186125
ABSTRACT
The spondyloepiphyseal dysplasia tarda (SEDT) is a hereditary arthropathy that progressively leads to deformities of small and large joints, irregularities of the end plates of vertebral bodies, which causes joint restriction, short stature, and gait difficulties. The typical radiographic findings of SEDT are generalized platyspondyly and dysplasia of the epiphyses, resulting in premature arthrosis. Clinically SEDT is manifested as a form of short-trunk dwarfism and early arthrosis in the period from late childhood to adolescence. The major clinical importance of this rare disease is similarity to juvenile idiopathic arthritis (JIA), which has a rather different prognosis and treatment. A few cases of SEDT have been published. However, no cases have been reported in South Korea. We describe the case of a 29-year old man who suffered from back and multiple joint pain, who was misdiagnosed as having ankylosing spondylitis. We evaluated the patient clinically and radiographically in greater detail, and changed his diagnosis to SED tarda.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Osteocondrodisplasias
/
Artrite Juvenil
/
Prognóstico
/
Espondilite Anquilosante
/
Anormalidades Congênitas
/
Artralgia
/
Doenças Raras
/
Nanismo
/
Epífises
/
República da Coreia
Tipo de estudo:
Estudo prognóstico
Limite:
Adolescente
/
Humanos
País/Região como assunto:
Ásia
Idioma:
Coreano
Revista:
Journal of Rheumatic Diseases
Ano de publicação:
2011
Tipo de documento:
Artigo
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