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dc.contributor.authorXue, Jing
dc.contributor.authorAlario, Anthony J.
dc.contributor.authorNelson, Scott D.
dc.contributor.authorWu, Huaxiang
dc.date2022-08-11T08:08:33.000
dc.date.accessioned2022-08-23T15:58:46Z
dc.date.available2022-08-23T15:58:46Z
dc.date.issued2013-10-01
dc.date.submitted2015-10-08
dc.identifier.citationSemin Arthritis Rheum. 2013 Oct;43(2):259-63. doi: 10.1016/j.semarthrit.2012.12.022. Epub 2013 Jan 24. <a href="http://dx.doi.org/10.1016/j.semarthrit.2012.12.022">Link to article on publisher's site</a>
dc.identifier.issn0049-0172 (Linking)
dc.identifier.doi10.1016/j.semarthrit.2012.12.022
dc.identifier.pmid23352250
dc.identifier.urihttp://hdl.handle.net/20.500.14038/30509
dc.description.abstractOBJECTIVES: To report an unusual case of lipoma aborescens (LA) presented in a patient with treatment-responsive juvenile spondyloarthropathy (JSPA) and to summarize the clinical manifestations, therapy and prognosis of LA by literature review. METHODS: We report an atypical case of a 17-year-old patient with an initial presentation of juvenile spondyloarthropathy, whose inflammatory condition was improved successfully by traditional anti-rheumatic drugs and an anti-TNF alpha agent but developed progressive swelling of bilateral knees. Lipoma arborescens were diagnosed in each knee by synovial biopsy obtained by arthroscopic surgery. Fifty-one cases of LA have been reported and are reviewed in detail. RESULTS: Clinically, LA could present as monoarthritis or oligoarthritis. The lateral compartment of the knee is the most common site of involvement. Several cases were reported as a comorbidity of inflammatory diseases, but were not improved by anti-inflammatory therapy. Most patients were diagnosed by classic MRI and biopsy findings. The lesions can be managed by open or arthroscopic surgery, but a minority of the cases may have reoccurrence in the same or opposite joint. CONCLUSIONS: LA is a very rare lesion of the synovial and bursal tissue with an unknown etiology. It is considered to be a benign proliferation of the synovial fat associated with trauma, degenerative or inflammatory conditions. LA should be considered as a secondary or comorbid condition in inflammatory arthropathies if other joints respond well to intensive therapy and one or more do not.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23352250&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.semarthrit.2012.12.022
dc.subjectAdolescent
dc.subjectArthroscopy
dc.subjectDisease Progression
dc.subjectFemale
dc.subjectHumans
dc.subjectKnee Joint
dc.subjectLipoma
dc.subjectSpondylarthropathies
dc.subjectTreatment Outcome
dc.subjectMusculoskeletal Diseases
dc.subjectNeoplasms
dc.subjectPediatrics
dc.subjectRheumatology
dc.titleProgressive bilateral lipoma arborescens of the knee complicated by juvenile spondyloarthropathy: a case report and review of the literature
dc.typeJournal Article
dc.source.journaltitleSeminars in arthritis and rheumatism
dc.source.volume43
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/787
dc.identifier.contextkey7693438
html.description.abstract<p>OBJECTIVES: To report an unusual case of lipoma aborescens (LA) presented in a patient with treatment-responsive juvenile spondyloarthropathy (JSPA) and to summarize the clinical manifestations, therapy and prognosis of LA by literature review.</p> <p>METHODS: We report an atypical case of a 17-year-old patient with an initial presentation of juvenile spondyloarthropathy, whose inflammatory condition was improved successfully by traditional anti-rheumatic drugs and an anti-TNF alpha agent but developed progressive swelling of bilateral knees. Lipoma arborescens were diagnosed in each knee by synovial biopsy obtained by arthroscopic surgery. Fifty-one cases of LA have been reported and are reviewed in detail.</p> <p>RESULTS: Clinically, LA could present as monoarthritis or oligoarthritis. The lateral compartment of the knee is the most common site of involvement. Several cases were reported as a comorbidity of inflammatory diseases, but were not improved by anti-inflammatory therapy. Most patients were diagnosed by classic MRI and biopsy findings. The lesions can be managed by open or arthroscopic surgery, but a minority of the cases may have reoccurrence in the same or opposite joint.</p> <p>CONCLUSIONS: LA is a very rare lesion of the synovial and bursal tissue with an unknown etiology. It is considered to be a benign proliferation of the synovial fat associated with trauma, degenerative or inflammatory conditions. LA should be considered as a secondary or comorbid condition in inflammatory arthropathies if other joints respond well to intensive therapy and one or more do not.</p>
dc.identifier.submissionpathfaculty_pubs/787
dc.contributor.departmentDepartment of Pediatrics
dc.source.pages259-63


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