A Single-Center Experience of Systemic Onset Juvenile Idiopathic Arthritis at a Tertiary Hospital in Jeddah, Saudi Arabia
Read full paper at:
http://www.scirp.org/journal/PaperInformation.aspx?PaperID=50688#.VEiUElfHRK0
http://www.scirp.org/journal/PaperInformation.aspx?PaperID=50688#.VEiUElfHRK0
Author(s)
Background and Objective: Systemic-onset juvenile
idiopathic arthritis (JIA) is a major and prevalent subset of arthritis
among children and it has a broad spectrum of clinical presentation,
course and prognosis. This study described the clinical presentation of
systemic-onset JIA in a Saudi-based cohort. Methods: A retrospective
chart review was performed of the medical records of children with
systemic-onset JIA who were followed up at King Abdul Aziz University
Hospital, Jeddah, between January 1997 and December 2013. Patients’
files were reviewed for demographic, clinical, and paraclinical data,
which were analyzed using the statistical Package for the Social
Sciences. Results: We included 20 patients of both genders (8 boys and
12 girls). The mean age of disease onset was 7 (4.5) years. The most
common presenting symptoms were fever (100%), arthritis (100%), and rash
(55%). Hepatomegaly (5%), abdominal (5%) and pulmonary manifestations
(3%) were less frequent manifestations. Most patients had high white
blood cell counts (50%), elevated erythrocyte sedimentation rates (80%)
and C-reactive protein levels (90%). The interval between onset of
symptoms and diagnosis was 9.4 (12.5) weeks. Patients were treated with
non-steroidal anti-inflammatory drugs, methotrexate, steroids,
anti-tumor necrosis agents, and disease-modifying anti-rheumatic drugs.
Bone marrow biopsy was conducted to exclude malignancy in 20% of the
patients. Conclusion: Saudi children with systemic-onset JIA present
with prolonged fever and arthritis (mainly oligoarticular rather than
polyarticular). Physicians should be aware of the presentation of
systemic-onset JIA in our setting in order to make prompt diagnosis and
treatment decisions as early as possible. Carful follow-up of febrile
patients is paramount to reaching the diagnosis early and initiating
treatment.
Cite this paper
Garout, W. and Muzaffer, M. (2014) A
Single-Center Experience of Systemic Onset Juvenile Idiopathic Arthritis
at a Tertiary Hospital in Jeddah, Saudi Arabia. Open Journal of Rheumatology and Autoimmune Diseases, 4, 212-218. doi: 10.4236/ojra.2014.44029.
[1] |
Yeh, T.L., Huang, F.Y., Shyur,
S.D., Chen, T.L., Lee, C.S. and Huang, D.T. (2010) Juvenile Idiopathic
Arthritis Presenting with Prolonged Fever. Journal of Microbiology,
Immunology and Infection, 43, 169-174. http://dx.doi.org/10.1016/S1684-1182(10)60027-8 |
[2] |
Tsai, H.Y., Lee, J.H., Yu, H.H.,
Wang, L.C., Yang, Y.H. and Chiang, B.L. (2012) Initial Manifestations
and Clinical Course of Systemic Onset Juvenile Idiopathic Arthritis: A
Ten-Year Retrospective Study. Journal of the Formosan Medical
Association, 111, 542-549. http://dx.doi.org/10.1016/j.jfma.2011.06.013 |
[3] |
Gurion, R., Lehman, T.J. and
Moorthy, L.N. (2012) Systemic Arthritis in Children: A Review of
Clinical Presentation and Treatment. International Journal of
Inflammation, 2012, Article ID: 271569. http://dx.doi.org/10.1155/2012/271569 |
[4] | Cimaz, R., Von Scheven, A. and Hofer, M. (2012) Systemic-Onset Juvenile Idiopathic Arthritis: The Changing Life of a Rare Disease. Swiss Medical Weekly, 142, w13582. |
[5] | De Benedetti, F. and Schneider, R. (2010) Systemic Juvenile Idiopathic Arthritis. In: Textbook of Pediatric Rheumatology, 6th Edition, Saunders. |
[6] | Schneider, R. and Laxer, R.M. (2008) Chap. 3: Systemic Juvenile Idiopathic Arthritis. In: Cimaz, R. and Lehman, T.J.A., Eds., Handbook of Systemic Autoimmune Diseases (Series Editor: Asherson, R.A.). Vol. 6: Pediatrics in Systemic Autoimmune Diseases, 35-54. |
[7] |
Cassidy, J.T., Levinson, J.E.,
Bass, J.C., Baum, J., Brewer Jr., E.J., Fink, C.W., Hanson, V., Jacobs,
J.C., Masi, A.T., Schaller, J.G., et al. (1986) A Study of
Classification Criteria for a Diagnosis of Juvenile Rheumatoid
Arthritis. Arthritis & Rheumatism, 29, 274-281. http://dx.doi.org/10.1002/art.1780290216 |
[8] |
Vastert, S.J., Kuis, W. and
Grom, A.A. (2009) Systemic JIA: New Developments in the Understanding of
the Pathophysiology and Therapy. Best Practice & Research Clinical
Rheumatology, 23, 655-664. http://dx.doi.org/10.1016/j.berh.2009.08.003 |
[9] |
Batthish, M., Schneider, R.,
Ramanan, A.V., Achonu, C., Young, N.L. and Feldman, B.M. (2005) What
Does “Active Disease” Mean? Patient and Parent Perceptions of Disease
Activity in the Systemic Arthritis Form of Juvenile Idiopathic Arthritis
(SO-JIA). Rheumatology (Oxford), 44, 796-799. http://dx.doi.org/10.1093/rheumatology/keh597 |
[10] | Bahabri, S., Al-Sewairi, W., Al-Mazyad, A., Karrar, A., Al-Ballaa, S., El-Ramahai, K., et al. (1997) Juvenile Rheumatoid Arthritis: The Saudi Experience. Annals of Saudi Medicine, 17, 413-418. |
[11] |
Singh-Grewal, D., Schneider, R.,
Bayer, N. and Feldman, B.M. (2006) Predictors of Disease Course and
Remission in Systemic Juvenile Idiopathic Arthritis: Significance of
Early Clinical and Laboratory Features. Arthritis & Rheumatism, 54,
1595-1601. http://dx.doi.org/10.1002/art.21774 |
[12] | Shishov, M., Henrickson, M., Burgos-Vargas, R., Rubio-Pérez, N., Baca, V., Romero-Feregrino, R, Solís-Vallejo, E., Huang, B., Grom, A.A. and Lovell, D.J. (2007) Systemic Features and Early Prognostic Factors in Hispanic and Non-Hispanic Children from the United States of America and Mexico with Systemic Juvenile Idiopathic Arthritis. Clinical and Experimental Rheumatology, 25, 907-914. |
[13] |
Spiegel, L.R., Schneider, R.,
Lang, B.A., Birdi, N., Silverman, E.D., Laxer, R.M., et al. (2000) Early
Predictors of Poor Functional Outcome in Systemic-Onset Juvenile
Rheumatoid Arthritis: A Multicenter Cohort Study. Arthritis &
Rheumatism, 43, 2402-2409. eww141023lx http://dx.doi.org/10.1002/1529-0131(200011)43:11<2402::AID-ANR5>3.0.CO;2-C |
评论
发表评论