Pediatric Acute Myeloid Leukemia: Unraveling Complexities in Intensive Chemotherapy and the Emergence of Superbugs - A Case Study.

Infect Drug Resist

Department of Haematology and Oncology, Shenzhen Children's Hospital, Shenzhen, Guangdong Province, People's Republic of China.

Published: October 2024

AI Article Synopsis

  • - The case report discusses a complex situation involving an 11-year-old boy with acute myeloid leukemia (AML) who faced significant challenges due to multidrug-resistant bacteria (CRPA) while undergoing chemotherapy.
  • - After initially achieving remission, the patient developed severe complications such as septic shock and bone marrow failure, necessitating changes in antibiotic treatment and revealing a highly resistant strain of CRPA through genomic analysis.
  • - The findings emphasize the need for reevaluating treatment approaches in pediatric AML cases and highlight the increasing issue of antimicrobial resistance, suggesting that more research is needed to improve patient outcomes.

Article Abstract

Background: This case report underscores the intricate challenges in managing paediatric patients with acute myeloid leukaemia (AML) undergoing intensive chemotherapy, particularly when complicated by the emergence of multidrug-resistant pathogens such as Carbapenem-Resistant (CRPA).

Case Presentation: An 11-year-old male with AML presented with skin purpura and persistent cough. Clinical and laboratory assessments revealed a high-risk AML profile with genetic mutations, leading to the initiation of intensive chemotherapy per the C-HUANA-AML-2015 protocol. Despite successful disease remission after initial chemotherapy courses, the patient experienced unexpected complications. Notably, septic shock, bone marrow failure, and the emergence of CRPA were encountered during the clinical course. Septic shock occurred following Course B3 chemotherapy, marked by a fever unresponsive to initial antibiotic therapy. Despite negative blood cultures, meropenem and vancomycin were initiated, successfully normalizing temperature. Subsequent challenges included persistent bone marrow suppression, perianal dermatitis, and the identification of CRPA in stool cultures, leading to altered antibiotic therapy guided by minimum inhibitory concentration (MIC) considerations. Whole-genome sequencing (WGS) of the CRPA strain revealed a highly virulent clone (ST-970) with numerous resistance and virulence genes.

Conclusion: This case report offers new insights into the complexities of pediatric AML management, with a focus on the emergence of CRPA. The discovery of a high-risk CRPA clone with detailed genomic data underscores the growing challenge of antimicrobial resistance in pediatric oncology. The persistent presence of CRPA and ongoing bone marrow failure highlight the difficulties in managing these complications. This case calls for a reassessment of treatment strategies and encourages further research to improve outcomes in pediatric AML, emphasizing the need for a multidisciplinary approach to address infectious complications and antimicrobial resistance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11471062PMC
http://dx.doi.org/10.2147/IDR.S478065DOI Listing

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