Pediatric Mucormycosis: A 10-Year Systematic Review of Reported Cases and Review of the Literature

Author:

Otto William R1ORCID,Pahud Barbara A23,Yin Dwight E23

Affiliation:

1. Department of Pediatrics, Division of Infectious Diseases, Children’s Hospital of Philadelphia, Pennsylvania

2. Department of Pediatrics, Division of Infectious Diseases, Children’s Mercy, Kansas City, Missouri

3. Department of Pediatrics, University of Missouri–Kansas City School of Medicine, Missouri

Abstract

AbstractMucormycosis is a severe infection that affects a variety of patients, including immunocompromised children and neonates. Given improved survival rates from advances in the treatment of malignancies, the population at risk for mucormycosis is increasing. We conducted a systematic review of cases of mucormycosis in children in the English-language literature reported between August 2008 and June 2017 and analyzed the clinical characteristics, diagnosis, management, and outcome of those infections. The most common underlying diagnoses included neutropenia (41%), hematologic malignancy (39%), prematurity (13%), and hematopoietic stem cell transplant (11%). Sinus disease (28%) and disseminated disease (24%) were the most common presentations. Rhizopus spp were the most common organisms isolated (22%). Amphotericin B remains the backbone of treatment and was prescribed in 86% of these cases. The resulting mortality rate remains high (32%). We provide here the results of a literature review of mucormycosis in children, including its epidemiology and clinical manifestations, and describe current advances in its diagnosis and treatment.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,General Medicine,Pediatrics, Perinatology and Child Health

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