Management of mycetoma: Major challenge in tropical mycoses with limited international recognition
Current Opinion in Infectious Diseases , Volume 20 - Issue 2 p. 146- 151
PURPOSE OF REVIEW: The present review highlights an orphan infectious disease in alarming need of international recognition. While money is being invested to develop new broad-spectrum antimicrobial drugs to treat infection in general, improvement in the management of complicated infections such as mycetoma receives little support. RECENT FINDINGS: Many case presentations describe single-center experience in the management of mycetoma. Unfortunately, randomized and blinded clinical studies into the efficacy of antimicrobial treatment are desperately lacking. Response to medical treatment is usually better in actinomycetoma than eumycetoma. Eumycetoma is difficult to treat using current therapies. Surgery in combination with azole treatment is the recommended regimen for small eumycetoma lesions in the extremities. Bone involvement complicates clinical management, leaving surgical amputation as the only treatment option. Although clinical management has not received major attention recently, laboratory technology has improved in areas of molecular diagnosis and epidemiology. SUMMARY: Management of mycetoma and laboratory diagnosis of its etiological agents need to be improved and better implemented in endemic regions. Optimized therapeutic approaches and more detailed epidemiological data are urgently needed. It is vital to initiate multicenter collaborations on national and international levels to develop consensus clinical score sheets and state-of-the-art treatment regimens for mycetoma patients.
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|Current Opinion in Infectious Diseases|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Ahmed, A.O.A, van de Sande, W.W.J, Fahal, A.H, Bakker-Woudenberg, I.A.J.M, Verbrugh, H.A, & van Belkum, A.F. (2007). Management of mycetoma: Major challenge in tropical mycoses with limited international recognition. Current Opinion in Infectious Diseases (Vol. 20, pp. 146–151). doi:10.1097/QCO.0b013e32803d38fe