Paraneoplastic vitelliform retinopathy in a patient with treated choroidal melanoma

Steven L. Williams; H. Richard McDonald; J. Michael Jumper; Arthur D. Fu; Brandon Lujan; Emmett T. Cunningham; Robert N. Johnson

Paraneoplastic vitelliform retinopathy in a patient with treated choroidal melanoma

Steven L. Williams, H. Richard McDonald, J. Michael Jumper, Arthur D. Fu, Brandon Lujan, Emmett T. Cunningham, Robert N. Johnson

Research output: Contribution to journal › Article

2 Scopus citations

Abstract

Purpose: To describe a peculiar case of paraneoplastic vitelliform maculopathy/retinopathy in a patient with treated choroidal melanoma. Methods: A case report of a 58-year-old woman with a history of treated choroidal melanoma 16 years before developing visual changes in the setting of metastatic choroidal melanoma. Results: We demonstrate bilateral, multifocal vitelliform subretinal lesions and focal, neurosensory retinal detachment associated with metastatic melanoma. Conclusion: Paraneoplastic vitelliform maculopathy/retinopathy should be considered in patients with or without a history of melanoma, who have unexplained serous, vitelliform retinal detachments, especially with atypical or absence of leakage on fluorescein angiography.

Original language	English (US)
Pages (from-to)	269-272
Number of pages	4
Journal	Retinal Cases and Brief Reports
Volume	8
Issue number	4
State	Published - 2014
Externally published	Yes

Keywords

Melanoma-associated retinopathy
Paraneoplastic vitelliform retinopathy

ASJC Scopus subject areas

Ophthalmology

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Williams, S. L., McDonald, H. R., Jumper, J. M., Fu, A. D., Lujan, B., Cunningham, E. T., & Johnson, R. N. (2014). Paraneoplastic vitelliform retinopathy in a patient with treated choroidal melanoma. Retinal Cases and Brief Reports, 8(4), 269-272.

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abstract = "Purpose: To describe a peculiar case of paraneoplastic vitelliform maculopathy/retinopathy in a patient with treated choroidal melanoma. Methods: A case report of a 58-year-old woman with a history of treated choroidal melanoma 16 years before developing visual changes in the setting of metastatic choroidal melanoma. Results: We demonstrate bilateral, multifocal vitelliform subretinal lesions and focal, neurosensory retinal detachment associated with metastatic melanoma. Conclusion: Paraneoplastic vitelliform maculopathy/retinopathy should be considered in patients with or without a history of melanoma, who have unexplained serous, vitelliform retinal detachments, especially with atypical or absence of leakage on fluorescein angiography.",

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AU - Williams, Steven L.

AU - McDonald, H. Richard

AU - Jumper, J. Michael

AU - Fu, Arthur D.

AU - Lujan, Brandon

AU - Cunningham, Emmett T.

AU - Johnson, Robert N.

PY - 2014

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N2 - Purpose: To describe a peculiar case of paraneoplastic vitelliform maculopathy/retinopathy in a patient with treated choroidal melanoma. Methods: A case report of a 58-year-old woman with a history of treated choroidal melanoma 16 years before developing visual changes in the setting of metastatic choroidal melanoma. Results: We demonstrate bilateral, multifocal vitelliform subretinal lesions and focal, neurosensory retinal detachment associated with metastatic melanoma. Conclusion: Paraneoplastic vitelliform maculopathy/retinopathy should be considered in patients with or without a history of melanoma, who have unexplained serous, vitelliform retinal detachments, especially with atypical or absence of leakage on fluorescein angiography.

AB - Purpose: To describe a peculiar case of paraneoplastic vitelliform maculopathy/retinopathy in a patient with treated choroidal melanoma. Methods: A case report of a 58-year-old woman with a history of treated choroidal melanoma 16 years before developing visual changes in the setting of metastatic choroidal melanoma. Results: We demonstrate bilateral, multifocal vitelliform subretinal lesions and focal, neurosensory retinal detachment associated with metastatic melanoma. Conclusion: Paraneoplastic vitelliform maculopathy/retinopathy should be considered in patients with or without a history of melanoma, who have unexplained serous, vitelliform retinal detachments, especially with atypical or absence of leakage on fluorescein angiography.

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