已发表论文

急性白血病的继发性眼部表现:临床模式与血液学相关性

 

Authors Yan BJ, Luo LH, Shen J, Huang YX

Received 4 March 2025

Accepted for publication 15 May 2025

Published 8 June 2025 Volume 2025:18 Pages 3289—3297

DOI https://doi.org/10.2147/JMDH.S522369

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Scott Fraser

Bo-Jing Yan,1 Li-Hua Luo,1 Jing Shen,2 Ying-Xiang Huang1 

1Department of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, People’s Republic of China; 2Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, People’s Republic of China

Correspondence: Ying-Xiang Huang, Email bshuang@163.com

Objective: To explore the clinical manifestations of secondary ocular changes in acute leukemia, classify these based on disease progression, investigate the etiology and treatment options for this rare retinal disease, and provide references for clinical management.
Methods: This cohort study was conducted in collaboration between the Department of Ophthalmology and Hematology at Beijing Friendship Hospital, Capital Medical University. A total of 74 acute leukemia patients admitted to the Hematology Department from January 2018 to September 2023 were enrolled. Ocular screenings were performed, and 34 patients with ocular symptoms were categorized and followed up. Clinical data differences were statistically analyzed based on hematologic diagnosis, and ocular manifestations and treatment outcomes were observed to identify optimal treatment approaches.
Results: Among the 74 patients, 34 (45.9%) exhibited ocular manifestations, with the majority being retinal changes (91.2%), mainly retinal hemorrhage or vascular occlusion. Ocular involvement in AML and ALL patients was classified into three severity levels, each corresponding to different treatments. Red blood cell hematocrit, white blood cell count, and platelet count were compared between AML and ALL patients with and without ocular involvement. Results showed that AML and ALL patients with retinal hemorrhage had lower hematocrit than those without ocular involvement (P< 0.05). Platelet counts were higher in AML and ALL patients with Roth spots than in those without ocular involvement (P< 0.05).
Conclusion: Acute leukemia remains a rare condition in ophthalmology practice in China. This study fills a diagnostic gap, providing valuable theoretical support for clinicians in terms of etiology, clinical manifestations, and treatment strategies.

Keywords: acute leukemia, secondary ocular manifestations, retinal vascular lesions, clinical treatment