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Conjunctival Pediatric-Type Follicular Lymphoma
Joseph O Okudolo1, Adam Bagg2, Beeran B Meghpara3,4
1Sidney Kimmel Medical College of Thomas Jefferson University.
Ophthalmic Plastic and Reconstructive Surgery
|December 24, 2019
Summary
Pediatric-type follicular lymphoma, a rare B-cell lymphoma, was diagnosed in the conjunctiva of a young adult. This case highlights a rare ocular manifestation and identifies a key MAP2K1 mutation.
Area of Science:
- Oncology
- Ophthalmology
- Hematology
Background:
- Pediatric-type follicular lymphoma (PTFL) is a rare B-cell neoplasm typically affecting pediatric and young adult head and neck lymph nodes.
- Ocular involvement by PTFL is exceptionally rare, with only five prior conjunctival cases documented.
Purpose of the Study:
- To report a rare case of conjunctival PTFL in a young adult.
- To detail the clinical presentation, pathological findings, and molecular characteristics of this unusual ocular lymphoma.
Main Methods:
- Clinical examination and excisional biopsy of conjunctival nodules.
- Immunohistochemistry (CD20, CD10, BCL6, BCL2), polymerase chain reaction (PCR) for immunoglobulin heavy chain rearrangement, fluorescence in situ hybridization (FISH), and next-generation sequencing (NGS).
Main Results:
- Biopsy revealed PTFL with characteristic germinal center morphology and immunophenotype (CD20+, CD10+, BCL6+, BCL2-).
- PCR confirmed a monoclonal B-cell population.
- NGS identified a pathogenic MAP2K1 mutation, a known genetic driver in PTFL.
Conclusions:
- Conjunctival PTFL is a rare but distinct entity that can mimic benign lesions like pyogenic granuloma.
- Molecular profiling, particularly identifying MAP2K1 mutations, is crucial for accurate diagnosis and understanding the pathogenesis of PTFL.
- This case expands the known spectrum of ocular involvement in PTFL and underscores the importance of comprehensive diagnostic workup for conjunctival masses.
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