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Case Reports
. 2019 Oct 21;4(3):253-256.
doi: 10.1177/2474126419880403. eCollection 2020 Jun.

Presumed Choroidal Metastasis From Oncocytic Carcinoma of the Parotid Gland: A Case Report

Affiliations
Case Reports

Presumed Choroidal Metastasis From Oncocytic Carcinoma of the Parotid Gland: A Case Report

Yousef J Cruz-Iñigo et al. J Vitreoretin Dis. .

Abstract

Purpose: This article reports a case of presumed choroidal metastasis from an oncocytic carcinoma of the parotid gland.

Methods: A 70-year-old man with history of an oncocytic carcinoma of the parotid gland presented owing to a 1-month history of progressive blurred central vision shortly after metastatic surveillance workup revealed liver, lung, and spine metastases. Fundus examination of the right eye showed a yellow choroidal mass surrounding the optic nerve and extending inferonasally, which is associated with subretinal fluid involving the foveal center. A-scan and B-scan ultrasonography were remarkable for a dome-shaped choroidal mass with medium-to-high internal reflectivity. Fluorescein angiography revealed pinpoint foci of hyperfluorescence over the choroidal lesion with late leakage. Magnetic resonance imaging of the brain showed evidence of metastatic disease to the cerebellum. While the patient underwent systemic chemotherapy, external beam radiotherapy was used to treat the eye.

Results: Four months later, visual acuity improved, the tumor reduced in size, and the subretinal fluid resolved. Systemic workup disclosed no new metastases.

Conclusion: Oncocytic carcinoma of the parotid gland is a rare and aggressive malignant neoplasm with frequent recurrences and distant metastases. The current case suggests that oncocytic carcinoma can metastasize to the choroid and, consequently, ocular metastasis surveillance is advised in these patients.

Keywords: choroidal metastasis; oncocytic carcinoma; parotid gland.

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Conflict of interest statement

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Wide-field fundus photography of the right eye showed a yellow choroidal mass surrounding the optic nerve and extending inferonasally posterior to the equator. Associated subretinal fluid temporal to the optic nerve was also noted.
Figure 2.
Figure 2.
B-scan ultrasonography of the right eye showed a dome-shaped choroidal mass with medium-to-high internal reflectivity and an apical height of 2.0 mm.
Figure 3.
Figure 3.
Wide-field fluorescein angiography of the right eye (left) revealed early-phase pinpoint foci of hyperfluorescence over the choroidal lesion with (right) late leakage.
Figure 4.
Figure 4.
Optical coherence tomography of the right eye showed a large, homogenous, hyporeflective, elevated area of choroidal infiltration temporal to the optic nerve, which is associated with overlying subretinal fluid involving the foveal center. Inner and outer retinal hyperreflective foci were also noted.

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