| Literature DB >> 23037580 |
A Desenfants1, E Huguon, Y Polfrit, M Crouzat, V Rouleau, V Chassot, L Besson-Leaud, I Missotte.
Abstract
In developed countries, Hansen disease, or leprosy, is a rare and little-known disease. Over the last few years, its prevalence in New Caledonia has remained stable (0.35 per 10,000 inhabitants). We report the case of an 11-year-old child who presented lepromatous leprosy complicated by a type 2 reaction. Despite appropriate treatment, the course was unusual with fever lasting a few weeks associated with asthenia, weight loss, and biological perturbations such as inflammatory syndrome, anemia, and hyperferritinemia. After a brief review of Hansen disease and its complications, we discuss the different hypotheses that can explain the clinical and biological progression of our patient (hemolytic anemia secondary to dapsone, type 2 reaction, and aspects of hemophagocytic syndrome) and describe therapeutic management, which led to a good outcome.Entities:
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Year: 2012 PMID: 23037580 DOI: 10.1016/j.arcped.2012.08.021
Source DB: PubMed Journal: Arch Pediatr ISSN: 0929-693X Impact factor: 1.180