Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Microbiol Immunol Infect ; 43(2): 93-8, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20457424

ABSTRACT

BACKGROUND/PURPOSE: The aim of the study was to investigate the clinical characteristics and nutritional status of juvenile rheumatoid arthritis (JRA) in Taiwanese children. METHODS: Fifty-three patients were included in this study. The disease subtype and patient characteristics were recorded. Body mass index (BMI) was determined. Seventy-five healthy age-matched children served as a control group. RESULTS: The inflammation parameters, including white blood cell count, platelet count, C-reactive protein, and erythrocyte sedimentation rate, were elevated in the systemic group. The BMI level of the JRA group was significantly lower than the control group (p = 0.006), especially in the male patients (p = 0.016) and when the patient age was greater than 4 (p = 0.011). The patients with oligoarticular onset JRA had significantly lower BMI compared with the healthy control group (p = 0.012). CONCLUSION: Nutritional status is often impaired in patients with JRA. The BMI of the JRA patients was lower than that of age-matched healthy children, especially in the male group, and when disease onset age was greater than 4. In our unselected sample, the most affected disease subtype was oligoarticular onset JRA.


Subject(s)
Arthritis, Juvenile/pathology , Nutritional Status , Age Factors , Body Mass Index , Case-Control Studies , Child , Child, Preschool , Female , Humans , Male , Sex Factors , Taiwan
2.
Acta Paediatr Taiwan ; 48(3): 149-51, 2007.
Article in English | MEDLINE | ID: mdl-17912988

ABSTRACT

Kimura's disease (KD) is a rare, chronic inflammatory disease, and the etiology is not yet to be determined. The disease is usually found in young Asian men but rarely in Western population. Here, we report an 8-year-old boy with the initial presentation of right upper eyelid swelling. Laboratory tests disclosed peripheral eosinophilia and elevated IgE level. KD with lacrimal gland involvement was diagnosed. Surgical excision was performed several times and steroid was also used, however the disease recurred. Thereafter, steroid, cyclosporine-A and azathioprine were prescribed. The tumor mass resolved and the laboratory data returned to normal level.


Subject(s)
Angiolymphoid Hyperplasia with Eosinophilia/therapy , Eyelid Diseases/therapy , Angiolymphoid Hyperplasia with Eosinophilia/etiology , Angiolymphoid Hyperplasia with Eosinophilia/pathology , Child , Eyelid Diseases/etiology , Eyelid Diseases/pathology , Humans , Male , Recurrence
SELECTION OF CITATIONS
SEARCH DETAIL
...