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Published on: March 22, 2012
Malassezia furfur bloodstream infection: still a diagnostic challenge in clinical practice
Rosalba Petruccelli1, Terenzio Cosio2,3, Valeria Camicia1
1Laboratory of Clinical Microbiology, Policlinico Tor Vergata, 00133, Rome, Italy.
Abstract:
The opportunistic fungus Malassezia furfur (M. furfur) can cause either cutaneous or systemic infections. We report a case of M. furfur fungemia in a 22-year-old male with T-cell Acute Lymphoblastic Leukemia (T-ALL) who developed concomitant Bacillus cereus (B. cereus) septicemia. The fungal infection was diagnosed by microscopic examination and culture-based methods, while automated blood culture systems and molecular approaches failed in identifying the fungus. Despite appropriate therapy, the patient died 18 days after the hospitalization.
Insights
A case of Malassezia furfur fungemia and Bacillus cereus septicemia occurred in a T-cell Acute Lymphoblastic Leukemia patient. Traditional methods diagnosed the fungus, unlike automated systems, but the patient did not survive.
Area of Science:
- Mycology
- Infectious Diseases
- Hematology
Background:
- Malassezia furfur is an opportunistic fungus causing cutaneous and systemic infections.
- T-cell Acute Lymphoblastic Leukemia (T-ALL) is a hematologic malignancy that can predispose patients to infections.
Observation:
- A 22-year-old male with T-ALL developed concurrent fungemia and bacteremia.
- The fungemia was caused by Malassezia furfur.
- The bacteremia was caused by Bacillus cereus.
Findings:
- Microscopic examination and culture successfully identified M. furfur fungemia.
- Automated blood culture systems and molecular methods failed to detect the fungal infection.
- The patient succumbed to the infections despite treatment.
Implications:
- Highlights the limitations of automated systems in diagnosing certain fungal infections like M. furfur.
- Emphasizes the importance of traditional diagnostic methods in immunocompromised patients.
- Underscores the severe prognosis of combined fungal and bacterial septicemia in T-ALL patients.
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