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Journal of Korean Medical Science ; : 481-483, 2004.
Article Dans Anglais | WPRIM | ID: wpr-228645

Résumé

Scleredema is a rare cutaneous mucinosis characterized by chronic diffuse induration of the skin, and it is occasionally associated with a monoclonal gammopathy (MG). Ankylosing spondylitis (AS) is noted to be another, chronic systemic inflammatory disorder of the axial skeleton that may accompany the MG. However, patients with scleredema and AS accompanied with a MG have not been reported in the literature. We here report a 40-yr-old man with scleredema and advanced AS accompanied with a MG of IgA-kappa protein. Widespread, long-standing scleredema has been developed over 10 yrs after the initial manifestation of AS. It is uncertain whether the coexistence of scleredema and AS is more than coincidental.


Sujets)
Adulte , Humains , Mâle , Collagène/métabolisme , Chaines légères kappa des immunoglobulines/composition chimique , Inflammation , Vertèbres lombales/imagerie diagnostique , Mucines/métabolisme , Paraprotéinémies/complications , Scléroedème de Buschke/complications , Peau/anatomopathologie , Pelvispondylite rhumatismale/complications
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