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Choroidal lymphoma: clinical features and association with systemic lymphoma
Arman Mashayekhi1, Shripaad Y Shukla1, Jerry A Shields1
1Ocular Oncology Service, Wills Eye Institute, Thomas Jefferson University, Philadelphia, Pennsylvania.
Ophthalmology
|August 28, 2013
Summary
Choroidal lymphoma (CL) often presents without systemic involvement, but secondary CL is morphologically high-grade and linked to severe ocular issues. Systemic evaluation is crucial for patients with CL lacking prior diagnosis of systemic lymphoma.
Area of Science:
- Ophthalmology
- Hematology
- Oncology
Background:
- Choroidal lymphoma (CL) is a rare malignancy affecting the eye.
- Understanding its clinical and histopathologic features is crucial for diagnosis and management.
- Association with systemic lymphoma impacts prognosis and treatment strategies.
Purpose of the Study:
- To detail the clinical and histopathologic characteristics of choroidal lymphoma.
- To investigate the association between choroidal lymphoma and systemic lymphoma.
- To differentiate between primary and secondary choroidal lymphoma.
Main Methods:
- Retrospective observational case series.
- Analysis of 59 patients (73 eyes) diagnosed with choroidal lymphoma.
- Review of clinical features, histopathology, and systemic lymphoma status.
Main Results:
- Systemic lymphoma was absent in 69% (primary CL) and present in 31% (secondary CL) of patients.
- Secondary CL exhibited more aggressive features, including higher rates of poor vision, bilateral involvement, and specific ocular manifestations.
- Secondary CL was morphologically higher grade (e.g., diffuse large cell lymphoma) compared to primary CL.
Conclusions:
- Secondary choroidal lymphoma is morphologically high-grade and presents with more severe ocular findings.
- Systemic evaluation is recommended for patients with CL without a known history of systemic lymphoma.
- Primary CL in this cohort did not show late development of systemic lymphoma.
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