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Disseminated fusariosis and hematologic malignancies, a still devastating association. Report of three new cases
Juan Carlos García-Ruiz1, Iñigo Olazábal1, Rosa María Adán Pedroso2
1Servicio de Hematología y Hemoterapia, BioCruces Health Research Institute, Hospital Universitario Cruces, Plaza de Cruces s/n, 48903 Barakaldo, Bizkaia, Spain.
Background:
Fungi of the genus Fusarium are primarily plant pathogens and saprobes that produce disseminated infections in immunologically deficient humans. After aspergillosis, disseminated fusariosis is the second most common cause of invasive infection by filamentous fungi in patients with hematologic malignancies or those undergoing transplants of hematopoietic progenitors.
Aims:
Disseminated fusariosis (DF) is considered an extremely rare infection and has reached a stable incidence rate, but its high mortality rate and the lack of an optimal management protocol have raised increasing interest in this mycosis.
Methods:
We present three cases of DF produced by Fusarium oxysporum species complex, Fusarium solani species complex and the highly unusual Fusarium dimerum in patients with advanced hematological malignancies diagnosed in our hospital between 2007 and 2011. The species level identification of the Fusarium isolates was established by sequencing their TEF1 gene.
Results:
The isolates showed low susceptibility to most of the antifungal agents analyzed, except that observed for F. dimerum to amphotericin B (AmB) and terbinafine, and F. oxysporum species complex to AmB. Interestingly, the strain of F. solani species complex exhibited high MIC values for AmB and voriconazole, notwithstanding these drugs were used for treatment with good results. Other relevant aspects to be considered in the treatment of DF are surgically cleaning foci of infection, withdrawing presumably contaminated catheters and recovery from neutropenia.
Conclusions:
The prevention of infection in colonized patients, the maintenance of a high level of diagnostic suspicion for early diagnosis, and the combined, vigorous and prolonged use of L-AmB and voriconazole are essential to decrease the mortality rate of this devastating infection.
Insights
Disseminated fusariosis (DF) is a rare but deadly fungal infection in immunocompromised patients. Early diagnosis and aggressive treatment with liposomal amphotericin B and voriconazole are crucial for survival.
Area of Science:
- Mycology
- Infectious Diseases
- Hematology
Background:
- Fusarium species cause disseminated infections in immunocompromised individuals, particularly those with hematologic malignancies.
- Disseminated fusariosis (DF) is the second most common invasive filamentous fungal infection in transplant recipients and cancer patients.
- Despite a stable incidence, DF has a high mortality rate and lacks standardized treatment protocols.
Observation:
- Three cases of DF caused by Fusarium oxysporum, Fusarium solani, and Fusarium dimerum in patients with advanced hematologic malignancies were analyzed.
- Species identification was performed using TEF1 gene sequencing.
- In vitro antifungal susceptibility testing revealed low susceptibility to most agents, with notable exceptions for F. dimerum and F. oxysporum.
Findings:
- Fusarium isolates demonstrated limited susceptibility to common antifungals.
- One Fusarium solani strain showed high minimum inhibitory concentrations (MICs) for amphotericin B (AmB) and voriconazole, yet responded well to treatment.
- Successful DF management involved antifungal therapy, surgical debridement of infection foci, catheter removal, and recovery from neutropenia.
Implications:
- Early diagnosis and prompt, aggressive treatment are vital for improving outcomes in disseminated fusariosis.
- Combined therapy with liposomal amphotericin B (L-AmB) and voriconazole is recommended for DF.
- Preventing infection in colonized patients and maintaining high diagnostic suspicion are key strategies.
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