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Early-onset Childhood Sarcoidosis with Incidental Multiple Enchondromatosis
Article in En | WPRIM | ID: wpr-39059
Responsible library: WPRO
ABSTRACT
The triad of rash, arthritis, and uveitis seems to be characteristic for early-onset childhood sarcoidosis. We describe an interesting case of early-onset childhood sarcoidosis coexisting enchondromatosis, which clinically masquerade as Langerhans cell histiocytosis. A 33 months old girl presented with skin rash, subcutaneous nodules with polyarthritis, and revealed the involvement of lymph nodes as well as spleen during work-up. She also presented with multiple osteolytic lesions which pathologically proven enchondromatosis. Oral prednisone was prescribed at 2 mg/kg/day for 2 months until when subcutaneous nodules and joint swellings almost disappeared, and then slowly tapered over a period of 5 months. We report an unusual case of early-onset childhood sarcoidosis presented with osteolytic bone lesions which were irrelevant to sarcoidosis.
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Full text: 1 Index: WPRIM Main subject: Arthritis / Sarcoidosis / Prednisone / Administration, Oral / Diagnosis, Differential / Enchondromatosis / Whole Body Imaging / Exanthema / Positron Emission Tomography Computed Tomography / Anti-Inflammatory Agents Type of study: Diagnostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Journal of Korean Medical Science Year: 2012 Type: Article
Full text: 1 Index: WPRIM Main subject: Arthritis / Sarcoidosis / Prednisone / Administration, Oral / Diagnosis, Differential / Enchondromatosis / Whole Body Imaging / Exanthema / Positron Emission Tomography Computed Tomography / Anti-Inflammatory Agents Type of study: Diagnostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Journal of Korean Medical Science Year: 2012 Type: Article