Scedosporium infection in immunocompromised patients:: Successful use of liposomal amphotericin B and itraconazole
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作者:
Barbaric, D
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Westmead Royal Alexandra Hosp Children, Childrens Hosp, Oncol Unit, Westmead, NSW 2145, AustraliaWestmead Royal Alexandra Hosp Children, Childrens Hosp, Oncol Unit, Westmead, NSW 2145, Australia
Barbaric, D
[1
]
Shaw, PJ
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Westmead Royal Alexandra Hosp Children, Childrens Hosp, Oncol Unit, Westmead, NSW 2145, AustraliaWestmead Royal Alexandra Hosp Children, Childrens Hosp, Oncol Unit, Westmead, NSW 2145, Australia
Shaw, PJ
[1
]
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[1] Westmead Royal Alexandra Hosp Children, Childrens Hosp, Oncol Unit, Westmead, NSW 2145, Australia
来源:
MEDICAL AND PEDIATRIC ONCOLOGY
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2001年
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37卷
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02期
Background. invasive fungal disease is a major cause of death in immunocompromised patients. The filamentous fungus Scedosporium consists of two species, S. prolificans and S. apiospermum, which can cause infections in immunocompromised patients that are often fatal. A significant feature of this pathogen is its broad resistance to many antifungal agents, including amphotericin B. Procedure and Results Five cases of infection with Scedosporium spp. occurred in patients with haematologic malignancies over a 10-month period. Three patients with S. prolificans were severely immunosuppressed and neutropenic; two were in relapse and another was early post-matched unrelated bone marrow transplant. All three died despite treatment with various combinations of amphotericin B and itraconazole. Two patients who were less immunosuppressed and had a normal neutrophil count developed S. apiospermum infection. Both were successfully treated with liposomal amphotericin B and itraconazole. Conclusions. Disseminated infection in immunocompromised hosts with Scedosporium spp. is often fatal. However, in patients with a lesser degree of immunocompromise and particularly in those infected with the less virulent S. apiospermum, intensive antifungal therapy with liposomal amphotericin B and itraconazole may be associated with complete eradication of infection. Med Pediatr Oncol 2001;37:122-125. (C) 2001 Wiley-Liss, Inc.
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Cuenca-Estrella, M
Ruiz-Díez, B
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Ruiz-Díez, B
Martínez-Suárez, JV
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Martínez-Suárez, JV
Monzón, A
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Monzón, A
Rodríguez-Tudela, JL
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Cuenca-Estrella, M
Ruiz-Díez, B
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Ruiz-Díez, B
Martínez-Suárez, JV
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Martínez-Suárez, JV
Monzón, A
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain
Monzón, A
Rodríguez-Tudela, JL
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Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, SpainInst Salud Carlos III, Ctr Nacl Microbiol, Unidad Micol, Madrid 28220, Spain