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Infantile leukemia presenting with cholestasis secondary to massive pancreatic infiltration

Dana R Rausch1, Karen I Norton, Ronald B J Glass

  • 1Department of Radiology, Mount Sinai School of Medicine, New York, NY 10029, USA.

Pediatric Radiology
|April 17, 2002
PubMed

Insights

A rare case of infantile leukemia caused pancreatic enlargement and neonatal cholestasis in a 10-week-old infant. This presentation highlights the need to consider leukemia in infants with unexplained cholestasis and pancreatic issues.

Area of Science:

  • Pediatric Hematology
  • Neonatal Gastroenterology
  • Medical Imaging

Background:

  • Neonatal cholestasis is a critical condition requiring prompt diagnosis.
  • Pancreatic enlargement is an uncommon finding in infants, especially in the context of leukemia.
  • Acute lymphoid leukemia (ALL) is rare in infants and typically presents differently.

Observation:

  • A 10-week-old infant presented with cholestasis and was found to have biliary obstruction due to massive pancreatic infiltration via ultrasound.
  • Diagnostic workup confirmed acute lymphoid leukemia (ALL) as the underlying cause.
  • The infant's pancreas showed significant enlargement, an unusual manifestation for both the age group and the disease.

Findings:

  • Massive pancreatic infiltration leading to biliary obstruction can be a presenting sign of infantile acute lymphoid leukemia (ALL).
  • Pancreatic enlargement in infants, while rare, should prompt consideration of hematologic malignancies.
  • Neonatal cholestasis may be an early indicator of leukemia in infants.

Implications:

  • This case underscores the importance of considering infantile leukemia in the differential diagnosis of neonatal cholestasis with pancreatic abnormalities.
  • Early recognition of leukemia in infants presenting with gastrointestinal symptoms can lead to timely intervention and improved outcomes.
  • Further research into the diverse presentations of infantile leukemia is warranted to enhance diagnostic capabilities.

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