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Bilateral Lacrimal Gland Lymphoma - Case Presentation
Violeta Ioana Prună1, Diana Mihaela Ciuc2, Valeriu Gabi Dincă3
1Department of Ophthalmology, CF2 Clinical Hospital, Bucharest, Romania.
Romanian Journal of Ophthalmology
|July 15, 2024
Summary
This case study details a rare bilateral lacrimal gland lymphoma, a type of non-Hodgkin lymphoma, in an 83-year-old male. Surgical intervention and corticosteroid therapy led to symptom improvement and tumor reduction.
Area of Science:
- Ophthalmology
- Oncology
- Pathology
Background:
- Lacrimal gland lymphomas are rare orbital tumors, comprising a small percentage of ocular adnexal malignancies.
- Orbital tumors can significantly impact visual function and require prompt diagnosis and management.
Observation:
- An 83-year-old male presented with bilateral lacrimal gland tumors, predominantly in the left orbit.
- Symptoms included decreased visual acuity, red eye, excessive tearing, and diplopia.
Findings:
- Initial evaluations suggested bilateral lacrimal gland lymphoma.
- Histopathology confirmed diffuse large B-cell non-Hodgkin lymphoma of the MALT type.
- Surgical intervention followed by corticosteroid therapy resulted in symptom improvement and tumor size reduction.
Implications:
- Comprehensive diagnostic approaches (clinical, imaging, histopathological) are crucial for rare orbital tumors.
- A multidisciplinary approach is essential for managing lacrimal gland lymphoma.
- Effective oncological management is vital for long-term disease control and patient well-being.
