Differentiation Syndrome; Post-ATRA/ATO Induction Therapy in Acute Promyelocytic Leukemia

Acute Promyelocytic Leukemia

Authors

  • Kanwal Karim Shalamar Nursing College, Lahore, Pakistan
  • Simab Pervaiz Shalamar Nursing College, Lahore, Pakistan
  • Ina Abdul Majeed The Aga Khan School of Nursing and Midwifery, Karachi, Pakistan
  • Sana Mushtaq Saida Waheed FMH College of Nursing, Lahore, Pakistan
  • Hina Arshad Saida Waheed FMH College of Nursing, Lahore, Pakistan

DOI:

https://doi.org/10.54393/pjhs.v4i10.1070

Keywords:

Acute, Promyelocytic, Leukemia, Differentiation Syndrome

Abstract

Acute promyelocytic leukemia (APL) is a disease described as definite morphological and cytogenetical abnormalities and leads to coagulopathy leaving the patient in a life-threatening condition. A specific chromosomal translocation of 15 and 17 chromosomes leads to retinoic acid receptor-α (RARα) and promyelocytic leukemia (PML) genes fusion that produces an abnormal gene mutation forming an oncogenic protein which is (PML-RARα). Those APL patients, who have been treated with all-trans retinoic acid (ATRA) or arsenic trioxide (ATO) commonly lead a complicated condition called differentiation syndrome which is rarely severe. This case report explains the 37-years old male diagnosed with acute promyelocytic leukemia and later developed a differentiation syndrome after initiation of all-trans retinoic acid and arsenic trioxide induction therapy.

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Published

2023-10-31
CITATION
DOI: 10.54393/pjhs.v4i10.1070
Published: 2023-10-31

How to Cite

Karim, K., Pervaiz, S., Majeed, I. A., Mushtaq, S., & Arshad, H. (2023). Differentiation Syndrome; Post-ATRA/ATO Induction Therapy in Acute Promyelocytic Leukemia: Acute Promyelocytic Leukemia. Pakistan Journal of Health Sciences, 4(10), 238–240. https://doi.org/10.54393/pjhs.v4i10.1070

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