01689nas a2200265 4500000000100000008004100001260001300042653001000055653002100065653001100086653001100097653002500108653001300133653000900146653001600155653001300171653001600184100001300200700001100213245007300224300001000297490000700307520109500314022001401409 2009 d c2009 Sep10aAdult10aErythema Nodosum10aFemale10aHumans10aLeprosy, lepromatous10aMalaysia10aMale10aMiddle Aged10aNecrosis10aYoung Adult1 aChoon SE1 aTey KE00aLucio's phenomenon: a report of three cases seen in Johor, Malaysia. a984-80 v483 a

BACKGROUND: Lucio's phenomenon is a rare and aggressive necrotising variant of erythema nodosum leprosum that classically occur in patients with undiagnosed, diffuse non-nodular lepromatous leprosy. It is a potentially fatal leprosy reaction characterised by extensive, bizarrely-shaped, painful purpuric skin lesions and ulcerations. Lucio's phenomenon is very rarely reported outside of Mexico and Costa Rica.

METHODS: We describe 3 cases seen in Johor, Malaysia.

RESULTS: The first two cases responded to the prompt simultaneous institution of daily rifampicin, dapsone, clofazimine and prednisolone. Case 3 continued to have new lesions and extension of existing lesions while on dapsone and clofazimine. The subsequent addition of rifampicin and prednisolone prevented new lesion formation but patient succumbed to the extensive cutaneous infarcts and consequent sepsis.

CONCLUSIONS: Early diagnosis and prompt institution of multi-drug therapy together with prednisolone may improve the prognosis and outcome of Lucio's phenomenon.

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