Pigmented villonodular synovitis of joints
Article first published online: 29 DEC 2010
Copyright © 2010 Wiley-Liss, Inc.
Journal of Surgical Oncology
Volume 103, Issue 5, pages 386–389, 1 April 2011
How to Cite
Mankin, H., Trahan, C. and Hornicek, F. (2011), Pigmented villonodular synovitis of joints. J. Surg. Oncol., 103: 386–389. doi: 10.1002/jso.21835
- Issue published online: 11 MAR 2011
- Article first published online: 29 DEC 2010
- Manuscript Accepted: 22 NOV 2010
- Manuscript Received: 14 SEP 2010
The objective of this study is to present two series of cases of pigmented villonodular disease of joints (PVNS) treated at different periods. The 215 cases from our hospital are current (1972–2009) and those 62 from the Jaffe collection from 1920 to 1968.
By use of our computerized tumor data system we were able to define age, gender, site, treatment, complications, and outcome. Examination of the material from the Jaffe collection included all of the above primary data but none on treatment and outcome.
The data for the two systems studied were remarkably similar. The average ages were in mid years and the disorder was more frequent in females. The largest numbers of cases for both series were in the knee and foot and less commonly in hip, shoulder, and hand. The treatments were mostly surgical excision with the exception of the hip which required total hip replacement. The results show only a small number of recurrences, no metastatic disease and no deaths.
Pigmented villonodular disease of joints is a rare entity, mostly occurring in the knee and foot. The principal treatment is surgical excision which is most often successful in these sites but leads to problems at other locations, especially the hip. J. Surg. Oncol. 2011; 103:386–389. © 2010 Wiley-Liss, Inc.