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Extranodal T/NK-cell lymphoma with fronto-orbital localization: A case report
Kaoutar Maslouhi1, Eric Michel Charlemagne Junior Kessi1, Salma Malak Ridah1
1Pediatric Radiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Pediatric orbito-cerebral lymphoma is a rare cancer impacting the eyes and brain. Early diagnosis and multimodal treatment, including chemotherapy and targeted therapies, improve outcomes for this challenging childhood malignancy.
Area of Science:
- Pediatric oncology
- Neuro-oncology
- Ophthalmology
Background:
- Orbito-cerebral lymphoma is a rare extranodal non-Hodgkin lymphoma predominantly affecting children.
- The condition impacts both the orbital and cerebral regions, presenting diagnostic challenges due to its mimicry of other diseases.
Observation:
- Symptoms are diverse, encompassing ocular, neurological, and systemic manifestations, often leading to delayed diagnosis.
- Magnetic Resonance Imaging (MRI) is the cornerstone for accurate diagnosis of pediatric orbito-cerebral lymphoma.
Findings:
- Treatment strategies combine chemotherapy, radiotherapy, and emerging targeted therapies, significantly enhancing patient survival rates.
- Prognosis is generally favorable for localized disease, whereas advanced stages or central nervous system involvement correlate with increased recurrence risk.
Implications:
- Improved diagnostic protocols and multimodal treatment approaches are crucial for managing this rare pediatric cancer.
- Long-term surveillance is essential for detecting recurrence and managing potential long-term side effects of treatment in survivors.
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