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CASE REPORT

Successful Treatment of Rare Pulmonary Coprinopsis cinerea Infection in a 17-Year-Old Female After Hematopoietic Stem Cell Transplantation: A Case Report

ORCID Icon, , , , , , , , , & show all
Pages 1567-1572 | Received 11 Nov 2022, Accepted 16 Mar 2023, Published online: 18 Mar 2023
 

Abstract

Invasive fungal infections (IFIs) are among the most severe complications in recipients of hematopoietic stem cell transplantation (HSCT) recipients and in patients with hematological malignancies. An increasing number of uncommon fungal infections have been reported in this era of antifungal prophylaxis. Coprinopsis cinerea is a rare pathogen that causes opportunistic infections in the immunocompromised patients, including HSCT recipients and is associated with very high mortality rates. Herein, we present a successfully treated pediatric HSCT patient with breakthrough pulmonary IFI caused by Coprinopsis cinerea despite posaconazole, prophylaxis using multidisciplinary approaches.

Ethical Approval and Consent for Participate

Written consents in approval for publication of this manuscript were obtained from both the patients and parents. The publication of this case report has been approved by Shenzhen Children’s Hospital Ethics Committee (approval number 2021102).

Consent for Publication

Written consent was obtained from the parents of the patient for the participation of this study.

Acknowledgments

We thank the patient and parents for giving the consent for the publication of this paper.

Author Contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Disclosure

The authors have no conflict of interests to declare for this work.

Additional information

Funding

This publication fee of this paper is funded by Shenzhen Science and Technology Innovation Commission (RCBS20200714114858018), Shenzhen Key Medical Discipline Construction Fund (SZXK034), Shenzhen Fund for Guangdong Provincial High-level Clinical Key Specialties (SZGSP012), Shenzhen High-level Hospital Construction Fund, Shenzhen Children’s Hospital Research fund (ynkt2021-zz26, ynkt2020-zz01).