CASE REPORT article

Front. Pediatr.

Sec. Pediatric Immunology

Volume 13 - 2025 | doi: 10.3389/fped.2025.1484145

Management of a pediatric patient with rapidly progressive glomerulonephritis and cutaneous mucormycosis:a case report

Provisionally accepted
  • 1Department of Pediatrics, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China
  • 2Department of Pediatrics, Jinling School of Clinical Medicine, Nanjing Medical University, Nanjing, China
  • 3National Clinical Research Center for Kidney Disease, Jinling Hospital, Nanjing Medical University, Nanjing, China

The final, formatted version of the article will be published soon.

Mucormycosis is a highly invasive and rare opportunistic infection caused by mucor fungi, characterized by challenging diagnosis and rapid disease progression. It predominantly affects patients with compromised immune systems due to various reasons, such as kidney failure, long-term use of antibiotics or corticosteroids. We recently successfully treated a pediatric patient with rapidly progressive glomerulonephritis accompanied by severe cutaneous mucormycosis. To our knowledge, this is the first reported case of rapidly progressive glomerulonephritis nephritis accompanied by dermatophytosis in a pediatric patient. In this case, we share our management experience, including special nursing experience. Cutaneous mucormycosis progresses quickly and is difficult to diagnose and treat, especially in children with compromised immune function, warranting high vigilance from clinicians and nursing staff. Early diagnosis and targeted treatment are crucial for improving the prognosis of patients. Therefore, once there is a suspicion of a mucormycosis infection, we recommend the early application of various testing methods such as fungal culture, skin biopsy and genetic testing in order to to promptly confirm the diagnosis.

Keywords: Rapidly progressive glomerulonephritis, Cutaneous mucormycosis, pediatric, Management, compromised immune function

Received: 21 Aug 2024; Accepted: 22 Apr 2025.

Copyright: © 2025 Jia, Shi, Sun, Xu, Sun and Gao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Chunlin Gao, Department of Pediatrics, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China

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