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Multicentric castleman disease with ocular involvement: a clinicopathologic case report
Geoffrey G Emerson1, Lyndell Lim, Marc Loriaux
1From the *Casey Eye Institute, Oregon Health & Science University, Portland, Oregon; the †Department of Pathology and Medicine, Oregon Health & Science University, Portland, Oregon; and ‡Health Associates of Peace Harbor, Florence, Oregon.
This case report details the first instance of multicentric Castleman disease affecting the eye. The rare lymphoproliferative disorder presented as bilateral choroidal infiltrates in a 69-year-old male patient.
Area of Science:
- Ophthalmology
- Hematology
- Pathology
Background:
- Castleman disease is a rare lymphoproliferative disorder.
- It typically involves lymph nodes in the abdomen, mediastinum, and cervical chain.
- Ocular involvement is uncommon.
Purpose of the Study:
- To describe a unique ocular manifestation of Castleman disease.
- To report the first clinicopathologic findings of multicentric Castleman disease involving the eye.
Main Methods:
- Clinicopathologic case report.
- Patient presented with lymphadenopathy and bilateral choroidal infiltrates.
- Diagnostic procedures included lymph node and choroidal biopsies.
Main Results:
- Lymph node biopsy confirmed Castleman disease without a monoclonal component.
- Choroidal biopsy revealed infiltration by lymphocytes and plasma cells.
- Initial suspicion of systemic lymphoma with ocular involvement was revised.
Conclusions:
- This is the first clinicopathologic report of multicentric Castleman disease presenting with ocular findings.
- Highlights the importance of considering Castleman disease in cases of unexplained choroidal infiltrates.
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