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[The infant with leukemia].

W A Kamps1, E J Sjamsoedin-Visser, E R van Wering

  • 1Stichting Nederlandse Werkgroep Leukemie bij Kinderen (SNWLK) te Den Haag.

Tijdschrift Voor Kindergeneeskunde
|April 1, 1988
PubMed
Summary

Infant leukemia is rare, and distinguishing it from leukemoid reactions requires cytogenetic analysis. Infants with leukemia face poor prognoses due to aggressive disease features and immature systems, necessitating specialized care and trials.

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NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols.

Leukemia·2010

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Cytogenetics

Context:

  • Infant leukemia presents unique diagnostic and therapeutic challenges.
  • Distinguishing leukemia from leukemoid reactions in newborns is critical.
  • Current treatment protocols are insufficient for this age group.

Purpose:

  • To highlight the diagnostic complexities of infant leukemia.
  • To outline the unfavorable prognostic factors in infant leukemia.
  • To emphasize the need for specialized therapeutic protocols and clinical trials.

Summary:

  • Infant leukemia, encompassing acute lymphoblastic, monoblastic, and undifferentiated types, is rare.
  • Poor prognostic indicators include high leukocyte counts, organomegaly, meningeal involvement, lack of common ALL antigen, and specific chromosomal translocations (e.g., 4;11).
  • Treatment is complicated by immature organ systems, requiring intensive supportive care.

Impact:

  • Underscores the need for precise cytogenetic analysis in neonates.
  • Highlights the poor outlook for infants diagnosed with leukemia.
  • Stresses the urgent requirement for novel therapeutic strategies and clinical trials in infant leukemia.

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