ArticleInternational journal of hematology2013
A case of Schizophyllum commune sinusitis following unrelated cord blood transplantation for acute lymphoblastic leukemia.
Article in International journal of hematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 16 citations in OpenAlex.
- Schizophyllum commune infection following chimeric antigen receptor T-cell therapy in a patient with lymphoma.Journal of clinical and experimental hematopathology : JCEH · 2025Article
- Pneumonia due toInfection & chemotherapy · 2022Article
- Article
- Schizophyllum radiatum, an Emerging Fungus from Human Respiratory Tract.Journal of clinical microbiology · 2016Article
- First report of otitis externa caused by Schizophyllum commune and review of the literature.Wiener klinische Wochenschrift · 2016Review
- Schizophyllum commune-induced allergic fungal rhinosinusitis and sinobronchial mycosis.Medical mycology case reports · 2015Article
- Reply to "implications of high antifungal susceptibility on Schizophyllum commune-associated allergy in clinical practice".Antimicrobial agents and chemotherapy · 2013Article
- Filamentous Basidiomycetes in the Clinical Laboratory.Current fungal infection reports · 2013Article
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Authors and funding
9 authors at 2 institutions in 1 country.
Funding
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Abstract
Schizophyllum commune is a globally distributed basidiomycete fungus that is known as a rare cause of sinusitis, for which no prompt treatment has been established. We describe the first report of S. commune sinusitis following unrelated cord blood transplantation for acute lymphoblastic leukemia. Thirteen days after transplantation, a 23-year-old female developed maxillary and ethmoid sinusitis. The sinusitis was antimicrobial-resistant, and the sinus aspirate culture revealed white wooly mold, which was identified as S. commune by nucleotide sequencing. The patient was successfully treated with intravenous administration of liposomal amphotericin B for 2 months, followed by oral voriconazole. This report suggests the effectiveness of liposomal amphotericin B and voriconazole for S. commune infection in immunocompromised patients. Given the difficulty in distinguishing S. commune infection from aspergillosis by standard culture methods, the incidence of S. commune infection following allogeneic hematopoietic stem cell transplantation may be underestimated. Nucleotide sequencing may be useful in the diagnosis of S. commune infection.
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