Invasive Rhino-Orbito-Cerebral Mucormycosis in Pediatric Patient with Acute Leukemia
Jazyk angličtina Země Česko Médium print
Typ dokumentu kazuistiky, časopisecké články
PubMed
32303134
DOI
10.14735/amko2020138
PII: 121921
Knihovny.cz E-zdroje
- Klíčová slova
- Rhizopus, acute leukemia, mucormycosis,
- MeSH
- akutní lymfatická leukemie farmakoterapie mikrobiologie chirurgie MeSH
- amfotericin B terapeutické užití MeSH
- antifungální látky terapeutické užití MeSH
- antitumorózní látky terapeutické užití MeSH
- centrální nervový systém mikrobiologie MeSH
- dítě MeSH
- lidé MeSH
- mukormykóza * farmakoterapie etiologie mikrobiologie chirurgie MeSH
- orbitocelulitida * farmakoterapie etiologie mikrobiologie chirurgie MeSH
- Rhizopus * MeSH
- sinusitida * farmakoterapie etiologie mikrobiologie chirurgie MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- amfotericin B MeSH
- antifungální látky MeSH
- antitumorózní látky MeSH
BACKGROUND: Invasive fungal infections are a life-threatening complication of cancer treatments, especially in hemato-oncological patients. Mucormycosis is the third leading cause of invasive fungal infections after Aspergillus and Candida infections. The first clinical symptoms are usually non-specific, which can lead to a late diagnosis and delayed therapy. PURPOSE: The objective of this report is to summarize data in the literature about mucormycosis and to present a case report of a patient with acute lymphoblastic leukemia, who developed this infection at our center. Risk factors for the development of mucormycosis, clinical symptoms, radiology, laboratory results, and outcome were retrospectively evaluated. CASE: We describe a 6-years-old female patient with acute lymphoblastic leukemia. During the induction phase of therapy, the patient developed febrile neutropenia and did not respond to therapy with a combination of antibiotics and supportive treatment. Pansinusitis and orbitocellulitis developed. Examination of the biological material revealed that the etiological agent was a Rhizopus sp. The patient was treated with a combination of antimycotic drugs, but the infection disseminated to the central nervous system. She underwent radical surgical resection of the affected tissue. At this time, she is still under treatment with antimycotic and oncology agents, but is in remission of the main diagnosis and in good clinical condition. CONCLUSION: Mucormycosis is an invasive fungal infection with high morbidity and mortality. Early diagnosis and initiation of effective therapy using a combination of amphotericin B administration and surgery are necessary to obtain a favorable outcome. The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.
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