Familial hypercholesterolemia misinterpreted as juvenile idiopathic arthritis
- PDF / 91,195 Bytes
- 1 Pages / 595.28 x 793.7 pts Page_size
- 61 Downloads / 203 Views
POSTER PRESENTATION
Open Access
Familial hypercholesterolemia misinterpreted as juvenile idiopathic arthritis AJ Schou*, P Toftedal, AE Christensen From 18th Pediatric Rheumatology European Society (PReS) Congress Bruges, Belgium. 14-18 September 2011 Background Early diagnosis is important in children with JIA to ensure early treatment and disease control. However, a wide range of diseases may mimic JIA causing overtreatment and delaying treatment of the underlying condition. Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder with elevated low density lipoprotein (LDL) and total cholesterol due to mutations with loss of function of the LDL-receptor. The condition predisposes to early atherosclerosis, coronary disease and stroke. Severely affected individuals may present with tendinous xanthomata, which may be mistaken for rheumatic nodules. Aim To describe a case of FH misinterpreted as JIA Methods A ten-year-old girl was transferred to our department for further follow-up and treatment. Three years earlier she developed tumours in several tendons including both Achilles-tendons and arthralgia. The tumours were interpreted as rheumatic nodules, which was supported by histological examination. She was thus diagnosed with JIA and treated with MTX and NSAID with no effect, on the contrary the tumours continued enlarging. Upon transferral to our department very high LDL and total cholesterol levels were found. The diagnosis FH was confirmed genetically; the biopsies were re-evaluated and now described as chronic granulomatous inflammation surrounding cholesterol-deposits. Cholesterol-lowering treatment (simvastatin) was started
lowering her blood values and the tumours were slowly regressing. Her mother had normal cholesterol-levels, her father died young of unrelated causes.
Conclusion FH is yet another rare, but important differential diagnosis to JIA. The case illustrates how important it is to continuously pay attention and ensure that working diagnosis is correct. Published: 14 September 2011
doi:10.1186/1546-0096-9-S1-P228 Cite this article as: Schou et al.: Familial hypercholesterolemia misinterpreted as juvenile idiopathic arthritis. Pediatric Rheumatology 2011 9(Suppl 1):P228.
Submit your next manuscript to BioMed Central and take full advantage of: • Convenient online submission • Thorough peer review • No space constraints or color figure charges • Immediate publication on acceptance • Inclusion in PubMed, CAS, Scopus and Google Scholar • Research which is freely available for redistribution
* Correspondence: [email protected] Hans Christian Andersen Children Hospital, Odense, Denmark
Submit your manuscript at www.biomedcentral.com/submit
© 2011 Schou et al; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Data Loading...
