Mucormycosis diagnosed during induction chemotherapy in five pediatric patients with acute lymphoblastic leukemia

Catherine Aftandilian1, Lourdes Eguiguren2, Roshni Mathew2

  • 1Pediatric Hematology/Oncology, Stanford University School of Medicine, Palo Alto, California.

Insights

Pediatric oncology patients with mucormycosis, a rare fungal infection, survived after modified chemotherapy and multidisciplinary care. Rapid diagnosis and treatment improved outcomes, even with disseminated disease during acute lymphoblastic leukemia treatment.

Area of Science:

  • Mycology
  • Pediatric Oncology
  • Infectious Diseases

Background:

  • Mucormycosis is a rare but severe fungal infection in pediatric oncology patients.
  • It is associated with high rates of morbidity and mortality, especially during intensive chemotherapy for acute lymphoblastic leukemia (ALL).

Purpose of the Study:

  • To describe the clinical characteristics and outcomes of pediatric patients with acute lymphoblastic leukemia who developed mucormycosis during induction chemotherapy.
  • To highlight the importance of early diagnosis and a multidisciplinary approach in managing this life-threatening infection.

Main Methods:

  • Retrospective case series of five pediatric patients diagnosed with mucormycosis during induction chemotherapy for ALL.
  • Chemotherapy regimens were modified to balance leukemia control with minimizing immunosuppression during antifungal treatment.

Main Results:

  • All five patients survived their mucormycosis infection, including those with disseminated disease.
  • Chemotherapy modification was successfully employed to manage both the leukemia and the fungal infection.
  • Rapid diagnosis and a multidisciplinary team approach were crucial for successful outcomes.

Conclusions:

  • Mucormycosis, despite its high fatality rate, can be effectively managed in pediatric oncology patients.
  • A tailored, multidisciplinary strategy involving modified chemotherapy and prompt antifungal treatment can lead to survival, even in complex cases of disseminated disease during intensive cancer therapy.

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
214
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
276
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
200
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
261
Diagnosing Acidosis and Alkalosis01:24

Diagnosing Acidosis and Alkalosis

Diagnosing acid-base imbalances involves systematically analyzing arterial blood samples, focusing on three key measurements: pH, bicarbonate (HCO3−) concentration, and carbon dioxide partial pressure (PCO2). This analysis follows a four-step process that helps identify the imbalance's underlying cause and nature.
First, the pH level is assessed to determine whether the blood pH is normal (7.35–7.45), low (acidosis), or high (alkalosis).
Next, the PCO2  and...
1.1K
Chemotherapy-Induced Nausea and Vomiting: Cannabinoids01:21

Chemotherapy-Induced Nausea and Vomiting: Cannabinoids

Tetrahydrocannabinol (THC) is a phytocannabinoid that primarily interacts with the CB1 receptor, a type of G protein-coupled receptor (GPCR) predominantly in and around the chemoreceptor trigger zone (CTZ) and emetic center. THC also blocks the serotonin receptor activity in the dorsal vagal complex (DVC) by inhibiting serotonin release. THC exerts its anti-emetic effects through these interactions, which are beneficial for patients undergoing chemotherapy.
Two synthetic agonists of THC,...
716