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Posaconazole as rescue therapy in African histoplasmosis

African histoplasmosis is a granulomatous mycosis caused by Histoplasma capsulatum var. duboisii. Treatment is usually extrapolated from guidelines for classical histoplasmosis, and includes 2–4 weeks of amphotericin B followed by a step-down maintenance therapy with itraconazole. Pediatric usage of...

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Detalles Bibliográficos
Autores principales: Gonçalves, Daniel, Ferraz, Catarina, Vaz, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427377/
https://www.ncbi.nlm.nih.gov/pubmed/23312726
http://dx.doi.org/10.1016/j.bjid.2012.06.027
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author Gonçalves, Daniel
Ferraz, Catarina
Vaz, Luisa
author_facet Gonçalves, Daniel
Ferraz, Catarina
Vaz, Luisa
author_sort Gonçalves, Daniel
collection PubMed
description African histoplasmosis is a granulomatous mycosis caused by Histoplasma capsulatum var. duboisii. Treatment is usually extrapolated from guidelines for classical histoplasmosis, and includes 2–4 weeks of amphotericin B followed by a step-down maintenance therapy with itraconazole. Pediatric usage of posaconazole, an oral second-generation azole, remains off-label, but recent surveys show that it is safe and well tolerated in children. We report a case of disseminated African histoplasmosis in a 12-year-old boy from Guinea-Bissau. Therapy with amphotericin B and itraconazole led to a progressive clinical deterioration. A dramatic and lasting improvement was observed using posaconazole. He completed 12 months of therapy. No relapse was noted during or 3 months after treatment. We report that posaconazole may be a safe and efficacious drug in the salvage management of disseminated AH, either in patients with disease refractory to conventional anti-fungal therapy, or in patients whose serious adverse effects of first-line drugs preclude its use.
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spelling pubmed-94273772022-09-01 Posaconazole as rescue therapy in African histoplasmosis Gonçalves, Daniel Ferraz, Catarina Vaz, Luisa Braz J Infect Dis Case Report African histoplasmosis is a granulomatous mycosis caused by Histoplasma capsulatum var. duboisii. Treatment is usually extrapolated from guidelines for classical histoplasmosis, and includes 2–4 weeks of amphotericin B followed by a step-down maintenance therapy with itraconazole. Pediatric usage of posaconazole, an oral second-generation azole, remains off-label, but recent surveys show that it is safe and well tolerated in children. We report a case of disseminated African histoplasmosis in a 12-year-old boy from Guinea-Bissau. Therapy with amphotericin B and itraconazole led to a progressive clinical deterioration. A dramatic and lasting improvement was observed using posaconazole. He completed 12 months of therapy. No relapse was noted during or 3 months after treatment. We report that posaconazole may be a safe and efficacious drug in the salvage management of disseminated AH, either in patients with disease refractory to conventional anti-fungal therapy, or in patients whose serious adverse effects of first-line drugs preclude its use. Elsevier 2013-01-09 /pmc/articles/PMC9427377/ /pubmed/23312726 http://dx.doi.org/10.1016/j.bjid.2012.06.027 Text en © 2013 Elsevier Editora Ltda. . https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Gonçalves, Daniel
Ferraz, Catarina
Vaz, Luisa
Posaconazole as rescue therapy in African histoplasmosis
title Posaconazole as rescue therapy in African histoplasmosis
title_full Posaconazole as rescue therapy in African histoplasmosis
title_fullStr Posaconazole as rescue therapy in African histoplasmosis
title_full_unstemmed Posaconazole as rescue therapy in African histoplasmosis
title_short Posaconazole as rescue therapy in African histoplasmosis
title_sort posaconazole as rescue therapy in african histoplasmosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427377/
https://www.ncbi.nlm.nih.gov/pubmed/23312726
http://dx.doi.org/10.1016/j.bjid.2012.06.027
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