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Buruli ulcer often starts as a painless swelling (nodule), a large painless area of induration (plaque) or a diffuse painless swelling of the legs, arms or face (oedema). The disease may progress with no pain and fever.

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Health Topic - 1 : Buruli ulcer (Mycobacterium ulcerans infection)
Definition:- Buruli ulcer is a chronic debilitating disease that mainly affects the skin and sometimes bones. First described by Sir Albert Cook in 1897 in Uganda, it was not until the 1930s that Australian scientists led by Peter MacCallum first succeeded in culturing the organism from lesions of patients from the Bairnsdale region. The name Buruli comes from an area of Uganda where many cases were reported in the 1960s. In Africa, about half of the patients are children under 15 years. In Australia, the average age is around 60 years. In 1998, WHO established the Global Buruli Ulcer Initiative in response to the growing spread of the disease, particularly in West Africa. Buruli ulcer is caused by Mycobacterium and belongs to the family of bacteria that causes tuberculosis and leprosy. Although the causative organism of the Buruli ulcer is an environmental bacterium, the mode of transmission to humans remains unknown. The organism produces a unique toxin – mycolactone – that causes damage to the skin. Early diagnosis and treatment are crucial to minimizing morbidity, costs and preventing long-term disability. Symptoms:- Symptoms of Buruli ulcer begin with painless nodules and swelling, usually on the arms and legs and sometimes on other parts of the body. These areas can then develop into large ulcers with a white and yellow base. M. ulcerans produces the toxin mycolactone. This has local immunosuppressive properties that enable the disease to progress rapidly with no pain and fever, making early detection difficult. However, if the ulcers are treated quickly, most will heal completely. If diagnosed late or left untreated, the condition can lead to scarring, permanent disfigurement and disability. Buruli ulcer has been reported in 33 countries in Africa, the Americas, Asia and the Western Pacific. Most cases occur in tropical and subtropical regions except in Australia, China and Japan. Out of the 33 countries, 14 regularly report data to WHO. Treatment:- Treatment consists of a combination of antibiotics and complementary treatments (under morbidity management and disability preventionehabilitation). Antibiotics: Current WHO recommendations are rifampicin 10 mg/kg per body weight daily and clarithromycin 7.5 mg/kg per body weight twice daily. Other interventions In addition to the antibiotics and depending on the stage of the disease, other interventions such as wound care, lymphedema management, surgery (mainly debridement and skin grafting to speed up healing) and physiotherapy are needed. Psychological support may also be needed for those with severe disease.

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