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Published on: September 11, 2013
Exudative retinal detachment in castleman disease
Gaetano R Barile1, Nora Khatib, Song Eun Lee
1From the *Department of Ophthalmology, and †Department of Pathology, Columbia University Medical Center, New York, New York.
Insights
Castleman disease (CD) can cause visual symptoms like retinal detachments. Systemic treatment for CD led to the resolution of these retinal issues without local therapy, highlighting a key observation for managing this rare condition.
Area of Science:
- Ophthalmology
- Hematology
- Oncology
Background:
- Castleman disease (CD) is a rare lymphoproliferative disorder.
- CD can present with diverse clinical manifestations, including ocular involvement.
- Visual symptoms and retinal disease are uncommon but significant presentations of CD.
Purpose of the Study:
- To document a case of Castleman disease presenting with visual disturbances.
- To describe the ocular findings, specifically retinal disease, in a patient with CD.
- To illustrate the management and outcome of retinal manifestations in CD.
Main Methods:
- Comprehensive clinical examination and fundus photography.
- Advanced imaging techniques including fluorescein and indocyanine green angiography.
- Diagnostic workup involving CT scans, blood tests, lymph node biopsy, and renal biopsy.
Main Results:
- A patient diagnosed with Castleman disease exhibited bilateral exudative retinal detachments.
- Systemic treatment with steroids for CD was initiated.
- Renal failure occurred during treatment but was successfully managed with plasmapheresis.
- The exudative retinal detachments resolved spontaneously within four weeks of systemic treatment initiation, without local ocular intervention.
Conclusions:
- Exudative retinal detachments can be a manifestation of Castleman disease.
- Systemic treatment for Castleman disease may lead to the resolution of associated retinal detachments.
- Observation of retinal changes under systemic therapy is a viable approach before considering local ocular treatments for CD-related retinal disease.
Purpose:
To describe the course of a case of Castleman disease (CD) that presented with visual symptoms and retinal disease.
Methods:
Clinical examination, fundus photography, and fluorescein and indocyanine green angiography were used to characterize the presence of bilateral exudative retinal detachments in a patient who was subsequently identified as having systemic lymphadenopathy.
Results:
After an extensive medical workup including CT scans, blood testing, and a lymph node and renal biopsy, the patient was diagnosed with CD. Steroids were administered to treat CD. During the course of treatment, the patient developed renal failure, which was successfully treated with plasmapheresis. Four weeks later, the bilateral retinal detachments had resolved without local treatment.
Conclusion:
Exudative retinal detachments as manifestations of CD may be observed under systemic treatment for resolution before considering local therapy.
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