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Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report
BACKGROUND: Fusarium spp. is being isolated with increasing frequency as a pathogen in oncohematologic patients. Caspofungin and amphotericin B have been reported to have synergistic activity against Fusarium spp. CASE PRESENTATION: We herein report a case of disseminated fusariosis diagnosed by che...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1878481/ https://www.ncbi.nlm.nih.gov/pubmed/17493279 http://dx.doi.org/10.1186/1471-2334-7-40 |
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author | Vagace, José-Manuel Sanz-Rodriguez, Cesar Casado, Maria-Soledad Alonso, Nieves Garcia-Dominguez, Manuel de la Llana, Francisco Garcia Zarallo, Luis Fajardo, Miguel Bajo, Roberto |
author_facet | Vagace, José-Manuel Sanz-Rodriguez, Cesar Casado, Maria-Soledad Alonso, Nieves Garcia-Dominguez, Manuel de la Llana, Francisco Garcia Zarallo, Luis Fajardo, Miguel Bajo, Roberto |
author_sort | Vagace, José-Manuel |
collection | PubMed |
description | BACKGROUND: Fusarium spp. is being isolated with increasing frequency as a pathogen in oncohematologic patients. Caspofungin and amphotericin B have been reported to have synergistic activity against Fusarium spp. CASE PRESENTATION: We herein report a case of disseminated fusariosis diagnosed by chest CT scan and positive blood cultures to Fusarium spp. Because the patient's clinical condition deteriorated, CRP levels increased, and blood cultures continued to yield Fusarium spp. despite liposomal amphotericin B monotherapy up to 5 mg/kg daily, treatment with caspofungin was added. Within 2 weeks of onset of combined antifungal therapy, the chest CT scan demonstrated a progressive resolution of the pulmonary lesions. Upon discontinuation of intravenous antifungals, the patient received suppressive therapy with oral voriconazole. Three months later, a chest CT scan showed no abnormalities. Twenty-five months after discontinuation of all antifungal therapy, the patient remains in complete remission of her neoplastic disease with no signs of clinical activity of the Fusarium infection. CONCLUSION: This is the first description of successful treatment of disseminated fusariosis in a pediatric patient with acute lymphoblastic leukemia with caspofungin and amphotericin B followed by oral suppressive therapy with voriconazole. |
format | Text |
id | pubmed-1878481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18784812007-05-29 Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report Vagace, José-Manuel Sanz-Rodriguez, Cesar Casado, Maria-Soledad Alonso, Nieves Garcia-Dominguez, Manuel de la Llana, Francisco Garcia Zarallo, Luis Fajardo, Miguel Bajo, Roberto BMC Infect Dis Case Report BACKGROUND: Fusarium spp. is being isolated with increasing frequency as a pathogen in oncohematologic patients. Caspofungin and amphotericin B have been reported to have synergistic activity against Fusarium spp. CASE PRESENTATION: We herein report a case of disseminated fusariosis diagnosed by chest CT scan and positive blood cultures to Fusarium spp. Because the patient's clinical condition deteriorated, CRP levels increased, and blood cultures continued to yield Fusarium spp. despite liposomal amphotericin B monotherapy up to 5 mg/kg daily, treatment with caspofungin was added. Within 2 weeks of onset of combined antifungal therapy, the chest CT scan demonstrated a progressive resolution of the pulmonary lesions. Upon discontinuation of intravenous antifungals, the patient received suppressive therapy with oral voriconazole. Three months later, a chest CT scan showed no abnormalities. Twenty-five months after discontinuation of all antifungal therapy, the patient remains in complete remission of her neoplastic disease with no signs of clinical activity of the Fusarium infection. CONCLUSION: This is the first description of successful treatment of disseminated fusariosis in a pediatric patient with acute lymphoblastic leukemia with caspofungin and amphotericin B followed by oral suppressive therapy with voriconazole. BioMed Central 2007-05-10 /pmc/articles/PMC1878481/ /pubmed/17493279 http://dx.doi.org/10.1186/1471-2334-7-40 Text en Copyright © 2007 Vagace et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Vagace, José-Manuel Sanz-Rodriguez, Cesar Casado, Maria-Soledad Alonso, Nieves Garcia-Dominguez, Manuel de la Llana, Francisco Garcia Zarallo, Luis Fajardo, Miguel Bajo, Roberto Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title | Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title_full | Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title_fullStr | Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title_full_unstemmed | Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title_short | Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
title_sort | resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1878481/ https://www.ncbi.nlm.nih.gov/pubmed/17493279 http://dx.doi.org/10.1186/1471-2334-7-40 |
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