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Published on: March 26, 2018
Pseudohypopyon in acute myelogeneous leukemia
1Department of Ophthalmology, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Insights
A child presented with eye inflammation and high eye pressure, initially mimicking other conditions. Further development revealed acute myelogenous leukemia, highlighting a rare presentation of this cancer.
Area of Science:
- Ophthalmology
- Pediatric Oncology
- Hematology
Background:
- Uniocular hypopyon, elevated intraocular pressure, and iris nodules are critical indicators of intraocular inflammation in pediatric patients.
- Differential diagnosis for these ocular findings in infants includes trauma, infection, retinoblastoma, and various histiocytic disorders.
- Early identification and accurate diagnosis are crucial for effective management and improved outcomes in pediatric eye conditions.
Observation:
- An 11-month-old boy presented with unilateral hypopyon, elevated intraocular pressure, and iris nodules.
- Initial investigations, including physical examination and laboratory tests, yielded normal results, complicating the diagnostic process.
- The child's condition evolved significantly over a three-week period.
Findings:
- The patient subsequently developed fulminant acute myelogenous leukemia (AML).
- This case underscores a rare and atypical presentation of AML in a pediatric patient.
- Ocular manifestations can precede or coincide with the systemic diagnosis of hematologic malignancies.
Implications:
- This case highlights the importance of considering hematologic malignancies in the differential diagnosis of pediatric uveitis and related ocular findings, even with initially normal investigations.
- Ophthalmologists and pediatricians should maintain a high index of suspicion for systemic diseases presenting with ocular symptoms.
- Prompt recognition of evolving symptoms is critical for timely diagnosis and management of life-threatening conditions like acute myelogenous leukemia.
Abstract:
An 11-month-old boy presented with uniocular hypopyon, elevated intraocular pressure, and iris nodules. A differential diagnosis of physical abuse, infection, retinoblastoma, juvenile xanthogranuloma, and histiocytosis X were considered but initial physical and laboratory investigations all had normal results. Three weeks following initial presentation, the child developed fulminant acute myelogenous leukemia. The clinical course, investigations, and outcome are reviewed.
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