Assessing Ocular Involvements in Childhood Leukemia Insights into Pathophysiology and Treatment

Malignancies Pediatric Leukemia Examination Ophthalmoscopy

Authors

  • Dr. Wisam Idham Jasim M.B.Ch.B., F.I.C.M.S. \ (Paediatrics) Iraqi Ministry of Health, Kirkuk Health Directorate, Kirkuk Teaching Hospital, Kirkuk, Iraq
  • Dr. Munther Saleh Abed Iraqi Ministry of Health, Kirkuk Health Directorate, Maternity and Children Hospital, Kirkuk, Iraq
  • Dr. Nihad Tariq Farage Iraqi Ministry of Health, Kirkuk Health Directorate, Maternity and Children Hospital, Kirkuk, Iraq
  • Dr. Ali Qais Abdulkafi M.B.Ch.B., D.C.H. \ (Pediatrics) Iraqi Ministry of Health, Kirkuk Health Directorate, Director of the Technical Affairs Department, Kirkuk Teaching Hospital, Kirkuk, Iraq
May 10, 2025

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Background: Malignancies such as acute leukemia-in its most common form in pediatric age groups-have been associated with eye involvements; these involvements may arise either because of the disease itself, its secondary complications, or side effects of therapy.

Aim of the study: To ascertain the prevalence of ocular involvement in leukemia patients.

Patients and Methods: Patients with leukemia were admitted to Nanakali Hematology and Oncology Hospital in Erbil from February 1 to May 31, 2024. This study included 120 eyes of 60 leukemia patients (58 with acute lymphoblastic leukemia and 2 with chronic myeloid leukemia). Patients' ages, sex, and hematological data were recorded. Their eyes were then examined for any lesions. This included determining visual acuity using a Snellen distance chart, flashlight anterior segment examination, slit-lamp examination, and dilated fundus examination with direct ophthalmoscopy. Ocular changes were correlated with hematological data.

Results: Ocular changes were seen in 23 patients with leukemia (38.3%), of which 22 were acute lymphoblastic leukemics, and 1 was chronic myeloid leukemia.

Conclusion: Ophthalmological manifestations in patients with Acute Leukemia are very common; these involvements can either be secondary to direct infiltration of leukemic cells or due to secondary causes of the disease or even treatment of the disease.

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