Müller-Weiss disease: Four case reports

• Published in: World journal of orthopedics 2020, Vol.11 (11), p.507-515
• Main Authors: Volpe, Antonio, Monestier, Luca, Malara, Teresa, Riva, Giacomo, Barbera, Giuseppe La, Surace, Michele Francesco
• Format: Report
• Language: English
• ISSN: 2218-5836; 2218-5836
• DOI: 10.5312/wjo.v11.i11.507

BACKGROUNDMüller-Weiss disease (MWD) is an idiopathic foot condition characterized by spontaneous tarsal "scaphoiditis" in adults. Frequently bilateral and affecting females during the 4th-6th decades of life, the pathogenesis of MWD remains unclear: It has been traditionally considered a spontaneous osteonecrosis of the navicular. The typical presentation of MWD is a long period of subtle discomfort followed by prolonged standing, atraumatic, disabling pain. Currently, there is no gold standard for the treatment of patients with MWD. Most support initial conservative therapy. Operative treatment should be considered for failure of conservative therapies longer than 6 months. The indication for surgery is severity of symptoms rather than severity of deformities. Operative treatment options include core decompression, internal fixation of the tarsal navicular, open or arthroscopic triple fusion, talo-navicular or talo-navicular-cuneiform arthrodesis, and navicular excision with reconstruction of the medial column. CASE SUMMARYIn this study, we report four patients affected by MWD. Clinical and radiographic assessment, follow-up and treatment are reported. CONCLUSIONAs it is frequently misdiagnosed, MWD is challenging for orthopedic surgeons. Early diagnosis and effective treatment are mandatory to avoid sequelae.