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Mycetoma

GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal

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Mycetoma — a chronic granulomatous infection of skin, subcutaneous tissue, fascia and bone caused by fungi (eumycetoma) or bacteria (actinomycetoma) — is a WHO Neglected Tropical Disease added to the NTD list in 2016, causing progressive, deforming, often amputation-requiring destruction of affected limbs, predominantly in the “mycetoma belt” stretching from Sudan through sub-Saharan Africa to South Asia and Latin America (WHO). Sudan accounts for approximately 70% of global mycetoma cases, predominantly caused by Madurella mycetomatis (eumycetoma). Treatment: itraconazole + surgery for eumycetoma; trimethoprim-sulfamethoxazole (+ amikacin for severe) for actinomycetoma. WHO targets 75% reduction in disability by 2030.

Key messages

WHO NTD since 2016 — Sudan carries 70% of burden
Mycetoma was added to the WHO Neglected Tropical Diseases list in 2016. Sudan accounts for approximately 70% of global mycetoma cases — with the Gezira state being the highest-burden area in the world (WHO).
Two types — fungal (eumycetoma) and bacterial (actinomycetoma)
Mycetoma is caused by either fungi (eumycetoma — Madurella mycetomatis most common, black grains) or bacteria (actinomycetoma — Nocardia, Actinomadura, Streptomyces — pale/white/yellow grains). The distinction determines treatment.
Painless progressive destruction
Mycetoma presents as a painless, slowly progressive swelling — typically of the foot (Madura foot), hand or knee — that forms sinuses (tracks to the surface) discharging coloured granules (the grains). Untreated, it progressively destroys skin, subcutaneous tissue, fascia and bone.
Amputation in approximately 30% of untreated cases
Without effective treatment, mycetoma causes progressive bone destruction and leads to amputation in approximately 30% of cases. Even with treatment, functional disability is common.
Itraconazole for eumycetoma, TMP-SMX for actinomycetoma
Treatment: eumycetoma — itraconazole (prolonged courses, often 12-24+ months, combined with surgery); actinomycetoma — trimethoprim-sulfamethoxazole (first-line, alone or with amikacin for 3-6+ months, then TMP-SMX maintenance). Response rates are modest and recurrence is common.
WHO 2030 target — 75% reduction in disability
WHO targets 75% reduction in mycetoma-related disability by 2030 through improved case detection, standardised treatment, access to medicines and research into new therapies.

Key statistics

~70%
of global mycetoma in Sudan
WHO
2016
year added to WHO NTD list
WHO
~30%
of untreated cases eventually require amputation
WHO
75%
WHO target reduction in disability by 2030
WHO NTD Roadmap
Farmers
and rural workers are highest-risk groups
WHO
Massively
underreported — true burden unknown
WHO

Mycetoma — global endemic distribution and relative burden

Source: WHO. The "mycetoma belt" runs from Sudan/Somalia through West Africa, India and Mexico/Venezuela.

Glossary of key terms

Eumycetoma
WHO
Fungal mycetoma — caused by true fungi, predominantly Madurella mycetomatis (responsible for approximately 70% of eumycetoma globally; produces black/dark brown granules). Other fungi: Scedosporium boydii, Fusarium, others. Responds partially to itraconazole (prolonged treatment); voriconazole or posaconazole for resistant cases. Surgery combined with antifungals.
Actinomycetoma
WHO
Bacterial mycetoma — caused by aerobic filamentous bacteria (actinomycetes): Nocardia brasiliensis (pale/white granules — most common in Latin America); Actinomadura madurae (white-yellow granules); Streptomyces somaliensis (yellow granules). More responsive to antibiotics than eumycetoma. First-line: TMP-SMX ± amikacin.
Grains (granules)
WHO/Pathology
The pathognomonic feature of mycetoma — aggregates of the causative organism embedded in a protein matrix. Discharged through sinuses (draining tracts) to the skin surface. Colour and morphology identify the causative organism: black (Madurella); white/pale (Actinomadura madurae, Nocardia); yellow (Streptomyces); red (Actinomadura pelletieri).
Madura foot
WHO/History
The historical name for mycetoma of the foot — first described by British physician Henry Van Dyke Carter in 1860 in Madurai district (India). Mycetoma of the foot (the most common anatomical site) was originally described as "Madura foot." Now any anatomical site can be affected.
Itraconazole for eumycetoma
WHO/DNDi
An azole antifungal — the most-used treatment for eumycetoma. Inhibits ergosterol synthesis in fungi. Response rates in M. mycetomatis eumycetoma: approximately 70-80% partial response; complete cure rare with antifungal alone. Combined with surgical debulking. Duration: often 12-24 months or longer.
Fosravuconazole (WHO/DNDi)
DNDi/research
A new azole antifungal prodrug of ravuconazole — in clinical development for eumycetoma through DNDI and the Mycetoma Research Centre (Khartoum). Phase 2/3 trials in Sudan. A potentially more effective oral option for M. mycetomatis eumycetoma.

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