Literature DB >> 24917565

Long-term follow-up results of primary and recurrent pigmented villonodular synovitis.

Floortje G M Verspoor1, Aniek A G Zee2, Gerjon Hannink2, Ingrid C M van der Geest2, Rene P H Veth2, H W Bart Schreuder2.   

Abstract

OBJECTIVE: Adequate documentation of the outcome of treatment of pigmented villonodular synovitis (PVNS) is sparse. Available case series show relatively short follow-up times and often combine locations or subtypes to increase patient numbers. This article describes the long-term follow-up of a single institution's large consecutive series of PVNS.
METHODS: Retrospectively, 107 PVNS patients were identified between 1985 and 2011 by searching pathology and radiology records. Treatment complications, recurrences and quality of life were evaluated. Most patients (85.2%) were primarily or secondarily treated at our institution.
RESULTS: Both subtypes, localized PVNS [29 (27%)] and diffuse PVNS [75 (70%)] were represented. The knee was affected in 88% of patients. Treatments received were surgery, external beam radiotherapy, radiosynovectomy, targeted therapy, immunotherapy or combinations of these. Forty-nine (46%) patients had prior treatment elsewhere. The mean follow-up from diagnosis until last contact was 7.0 years (range 0.3-27.4) for localized PVNS and 14.5 years (range 1.1-48.7) for diffuse PVNS. The 1- and 5-year recurrence-free survival rates for diffuse PVNS were 69% and 32%, respectively. Quality of life, estimated by 36-item Short Form Health Survey (SF-36) scores, were not significantly different between localized and diffuse PVNS. However, both patient groups scored lower than the general population norms on the general health component (59.2 and 56.3, respectively, P < 0.05).
CONCLUSION: Recurrence rates of PVNS increase with time. Long-term follow-up shows, particularly in diffuse PVNS, it is a continually recurring problem, and over time it becomes increasingly difficult to cure. The quality of life is decreased in patients with PVNS compared with the general population.
© The Author 2014. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  follow-up studies; pigmented villonodular; quality of life; synovitis; therapy; treatment outcome

Mesh:

Year:  2014        PMID: 24917565     DOI: 10.1093/rheumatology/keu230

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  20 in total

1.  Clinical outcomes of diffuse PVNS of the knee following arthroscopic complete synovectomy±posterior open resection.

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2.  Immune Cell Infiltration Characteristics of Pigmented Villous Nodular Synovitis and Prediction of Potential Diagnostic Markers Based on Bioinformatics.

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Review 3.  Current Systemic Treatment Options for Tenosynovial Giant Cell Tumor/Pigmented Villonodular Synovitis: Targeting the CSF1/CSF1R Axis.

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4.  Arthroplasty for tenosynovial giant cell tumors.

Authors:  Floortje G M Verspoor; Gerjon Hannink; Anouk Scholte; Ingrid C M Van Der Geest; H W Bart Schreuder
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Review 5.  Multifocal pigmented villonodular synovitis coexisting in both the knee joint and the patella: a case report and literature review.

Authors:  Mingxuan Gao; Hong Li; Xiaoyan Liang; Xiaoyan Fu; Xusheng Li
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6.  Limb Amputation after Multiple Treatments of Tenosynovial Giant Cell Tumour: Series of 4 Dutch Cases.

Authors:  Monique J L Mastboom; Floortje G M Verspoor; Hans Gelderblom; Michiel A J van de Sande
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8.  Patient-reported Symptoms of Tenosynovial Giant Cell Tumors.

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Journal:  Clin Ther       Date:  2016-04-01       Impact factor: 3.393

9.  The Patient Perspective on the Impact of Tenosynovial Giant Cell Tumors on Daily Living: Crowdsourcing Study on Physical Function and Quality of Life.

Authors:  Monique Josephine Mastboom; Rosa Planje; Michiel Adreanus van de Sande
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10.  Economic burden and health-related quality of life in tenosynovial giant-cell tumour patients in Europe: an observational disease registry.

Authors:  J Lopez-Bastida; I Aranda-Reneo; B Rodríguez-Sánchez; L M Peña-Longobardo; X Ye; P Laeis; E M Fronk; E Palmerini; A Leithner; M A J Van de Sande
Journal:  Orphanet J Rare Dis       Date:  2021-07-02       Impact factor: 4.123

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