| Literature DB >> 20216127 |
Aarat M Patel1, Amanda G Brown, Csaba Galambos, Raphael Hirsch.
Abstract
We describe a child with pigmented villonodular synovitis initially treated for a presumed hip infection. The correct diagnosis was not made until 2(1/2) years later on a second admission. This is a rare disease with vague presenting symptoms that requires a high index of suspicion. Magnetic resonance imaging and tissue biopsy are usually needed for a definitive diagnosis. Surgery is the primary treatment option; however, the patient described was unusual in that she did well to date with conservative measures.Entities:
Mesh:
Year: 2010 PMID: 20216127 PMCID: PMC3947543 DOI: 10.1097/RHU.0b013e3181cf8657
Source DB: PubMed Journal: J Clin Rheumatol ISSN: 1076-1608 Impact factor: 3.517