The long-term progression of macrodactyly. (March 2022)

• Record Type: Journal Article
• Authors: Stor, Merel L.E.; Lokhorst, Max M.; Horbach, Sophie E.R.; van der Horst, Chantal M.A.M.
• Is Part Of: JPRAS open. Volume 31(2022)
• Page Start: 10
• Page End: 21
• Publication Date: 2022-03
• Subjects: Macrodactyly -- macrodystrophia lipomatosa -- overgrowth -- PIK3CA; Surgery, Plastic -- Great Britain -- Periodicals; 617.9505
• DOI: 10.1016/j.jpra.2021.10.004
• Languages: English
• ISSNs: 2352-5878

Abstract

Abstract: Background: Macrodactyly is a rare congenital disorder of overgrowth affecting the digits of the upper or lower extremity. Mostly, patients are surgically treated during childhood to reduce the digit or to stop growth. There are no standardized guidelines for the treatment and follow-up of macrodactyly. Consequently, follow-up may not be regularly scheduled into adulthood. Methods: A retrospective, descriptive analysis of patients with the long-term progression of macrodactyly who presented at our tertiary referral hospital between July 2018 and March 2020 was performed. All patients from our local macrodactyly database were screened for progression of macrodactyly since adulthood; this resulted in four patients. The aim of these case series is to highlight the clinical features and disease course at long-term follow-up. Results: All patients were surgically treated during childhood and showed progression of tissue overgrowth during adult life. All patients developed severe secondary degenerative bone changes in macrodactyly affected digits, such as ankyloses of joints, new bone formation, and bony spurs. Subsequently, tissue overgrowth and degenerative bone changes led to functional problems. Conclusion: Patients with macrodactyly may experience growth during adult life, which may progress to deforming changes. Consequently, patients should be informed about the possible growth, and the progressive growth should be monitored.