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. 2012;5(5):625-9.
doi: 10.3980/j.issn.2222-3959.2012.05.16. Epub 2012 Oct 18.

Retinoblastoma in a young adult mimicking Coats' disease

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Retinoblastoma in a young adult mimicking Coats' disease

Zheng Zhang et al. Int J Ophthalmol. 2012.

Abstract

Retinoblastoma is the most common childhood primary intraocular malignancy, with the majority of cases being diagnosed before 5 years of age. Retinoblastoma in adults is extremely rare. Here, we report the case of a 20-year-old man who presented with a 3 year history of blurred vision in the right eye. Imaging did not reveal the typical presentation of retinoblastoma. After considering Coats' disease, a diagnosis of late-presenting retinoblastoma was made through cytological analysis. Diagnosis of retinoblastoma should be considered in the presence of uncertain mass lesions in the fundus of an adult.

Keywords: Coats'disease; adult; cytological analysis; retinoblastoma.

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Figures

Figure 1
Figure 1. Ultrasonographic examination of the right eye showing a moderately reflective material occupying the nasal peripheral retina that was suggestive of a mass with a collection of fluid beneath the retina, a highly reflective lesion can be seen in the mass. The left eye was sound.
Figure 2
Figure 2. Computed tomography (CT) showing the mass involving the nasal retina with a minimal higher density and without calcification in the right eye.
Figure 3
Figure 3. A: Axial T1-weighted MR image showing the mass involving the ciliary body, which had slightly higher signal intensity; B: Axial T2-weighted MR image showing the mass had a relatively low-intensity signal; C: The contrast-enhanced MR image showing there was diffuse enhancement of the mass.
Figure 4
Figure 4. Cytological analysis of the anterior chamber puncture fluid showing neoplastic cells forming loosely cohesive clusters. Note the scant cytoplasm, the high nuclear to cytoplasmic ratio (staining by hematoxylin-eosin; original magnification, ×400).
Figure 5
Figure 5. A: The tumor was present in the anterior segment and implanted into the iris and ciliary body with neovascularization on the anterior surface of the iris (staining by hematoxylin-eosin; original magnification, ×40). B: The tumor was found to have invaded the optic nerve head without any extension to the lamina cribrosa and optic nerve (staining by hematoxylin-eosin; original magnification, ×40). C: The presence of a classical Homer-Wright rosette pattern (staining by hematoxylin-eosin; original magnification, ×100).

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