Literature DB >> 23037580

[Leprosy with an unusual course].

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.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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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


  1 in total

1.  A case of leprosy, erythema nodosum leprosum, and hemophagocytic syndrome: A continuum of manifestations of same agent-host interactions.

Authors:  Prasan Kumar Panda; Ramjas Prajapati; Arvind Kumar; Manisha Jana; Pradeep Immanuel; Pranay Tanwar; Naveet Wig
Journal:  Intractable Rare Dis Res       Date:  2017-08
  1 in total

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