02195nas a2200217 4500000000100000008004100001260001200042653003100054653001600085653002300101653001200124100001700136700001300153700001400166245008900180856009300269300000800362490000700370520158600377022001401963 2024 d c12/202410aMycobacterium lepromatosis10aCase report10aHansen’s disease10aleprosy1 aAkhverdyan N1 aCantor Z1 aHawkins K00aAn alternative multidrug regimen for multibacillary Hansen's disease: a case report. uhttps://jmedicalcasereports.biomedcentral.com/counter/pdf/10.1186/s13256-024-04971-9.pdf a1-40 v183 a
Background: Leprosy (Hansen's disease) is an infectious disease most common in resource-limited countries caused by the acid-fast bacilli Mycobacterium leprae and Mycobacterium lepromatosis that frequently affects the skin and peripheral nerves. Prompt diagnosis and treatment with multidrug therapy is crucial to reduce disease transmission and sequelae, which include nerve function impairment, ocular injury, and stigmatizing physical deformities. Traditional treatment of multibacillary leprosy consists of 12-24 months of multidrug therapy with dapsone, rifampin, and clofazimine. However, this regimen is associated with high pill burden and side effects that limit adherence.
Case presentation: We report a case of multibacillary leprosy in a previously healthy 30-year-old Hispanic man who recently immigrated to the USA from South America and presented with progressive nodular skin lesions on his face and extremities. He was treated with a monthly regimen of rifampin, moxifloxacin, and minocycline. At follow-up there was significant improvement of his cutaneous lesions without signs of reversal reaction or erythema nodosum leprosum.
Conclusions: This case report adds to the growing repertoire of literature supporting the use of rifampin, moxifloxacin, and minocycline. Further studies are needed to assess the efficacy of this antimycobacterial regimen and monitor rates of relapse and delayed immunologic reactions, which may occur 5-10 years after completion of treatment.
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