A Case of Spondyloepiphyseal Dysplasia Tarda (SEDT) Misdiagnosed as Ankylosing Spondylitis.
10.4078/jrd.2011.18.4.311
- Author:
Il Hwan OH
1
;
June Seok SONG
;
Dong Hwi RIM
;
Jong Wook CHOI
;
Seunghun LEE
;
Joo Hyun LEE
;
Tae Hwan KIM
Author Information
1. Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea. thkim@hanyang.ac.kr
- Publication Type:Case Report
- Keywords:
Spondyloepiphyseal dysplasia tarda;
Ankylosing spondylitis;
Juvenile idiopathic arthritis
- MeSH:
Adolescent;
Arthralgia;
Arthritis, Juvenile Rheumatoid;
Congenital Abnormalities;
Dwarfism;
Epiphyses;
Gait;
Humans;
Joints;
Osteochondrodysplasias;
Prognosis;
Rare Diseases;
Republic of Korea;
Spondylitis, Ankylosing
- From:Journal of Rheumatic Diseases
2011;18(4):311-314
- CountryRepublic of Korea
- Language:Korean
-
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.
