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Published on: October 26, 2011
Malassezia: is it a pulmonary pathogen in the stem cell transplant population?
A H Blaes1, W P Cavert, V A Morrison
1Division of Hematology/Oncology/Transplantation, Veterans Affairs Medical Center, University of Minnesota, Minneapolis, Minnesota 55455, USA. blaes004@umn.edu
Abstract:
Malassezia furfur is a yeast that can cause a variety of infections, most commonly in normal hosts, and also in immunocompromised hosts. This yeast typically colonizes the skin, and is the causative agent of tinea versicolor. However, in immunocompromised hosts, it can more commonly cause catheter-related fungemia or folliculitis. Pulmonary infections from Malassezia have not been commonly recognized. Unlike many other common opportunistic fungal infections in immunocompromised hosts, neutropenia and the use of broad-spectrum antibiotics do not appear to be significant risk factors for Malassezia infections in the stem cell transplant (SCT) population. Additionally, disseminated infection, despite fungemia, is uncommon. A series of patients who underwent SCT at the University of Minnesota between 2004 and 2006 were reviewed for the occurrence of suspected Malassezia infections in the post-transplant period. Four cases of possible pulmonary M. furfur infection were identified in our SCT recipients. The clinical characteristics of these patients, the infections, treatment, and outcome are described. In addition, we discuss the possible pathogenicity of this yeast in the pulmonary setting.
Insights
Malassezia furfur can cause lung infections in stem cell transplant patients. Unlike other fungi, neutropenia is not a risk factor, and disseminated disease is rare.
Area of Science:
- Mycology
- Infectious Diseases
- Immunocompromised Hosts
Background:
- Malassezia furfur is a yeast commonly causing skin infections like tinea versicolor.
- In immunocompromised individuals, it can lead to catheter-related fungemia or folliculitis.
- Pulmonary infections by Malassezia are rarely documented, especially in stem cell transplant (SCT) recipients.
Observation:
- This study reviewed SCT recipients at the University of Minnesota from 2004-2006.
- Four cases of suspected pulmonary Malassezia furfur infection were identified post-transplant.
- Clinical characteristics, infection details, treatment, and outcomes were analyzed.
Findings:
- Malassezia infections in SCT patients may manifest as pulmonary disease.
- Neutropenia and broad-spectrum antibiotics are not significant risk factors for Malassezia in SCT.
- Disseminated infection is uncommon even with fungemia.
Implications:
- Highlights the potential for Malassezia furfur to cause pulmonary infections in SCT recipients.
- Suggests a need to consider Malassezia in the differential diagnosis of pulmonary infections in this population.
- Contributes to understanding the pathogenicity of Malassezia in non-cutaneous settings.
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