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Case Reports
. 2022 May 20:12:Doc11.
doi: 10.3205/oc000198. eCollection 2022.

Multimodal imaging of a sporadic retinal astrocytic hamartoma simulating retinoblastoma in a newborn

Affiliations
Case Reports

Multimodal imaging of a sporadic retinal astrocytic hamartoma simulating retinoblastoma in a newborn

Bilge Batu Oto et al. GMS Ophthalmol Cases. .

Abstract

Introduction: To report a sporadic astrocytic hamartoma simulating retinoblastoma in a newborn.

Methods: Clinical data was reviewed retrospectively.

Results: A 3-month-old baby with a history of perinatal asphyxia was referred to our ocular oncology clinic with suspected retinoblastoma in the left eye. Dilated fundoscopy revealed a solitary tumor covering the optic disc at the left eye. The whitish-yellow lesion was well-defined, opaque, and minimally calcified. High internal reflectivity and posterior shadowing due to the intralesional calcification, and intratumoral cystic spaces were observed in B-scan ultrasound imaging. Optical coherence tomography imaging showed an intraretinal tumor with cystic spaces and posterior shadowing. The tumor was diagnosed as an astrocytic hamartoma. The systemic evaluation was negative for phacomatoses. The lesion has been observed with multimodal imaging for six years without significant changes.

Conclusions: Retinal astrocytic hamartomas are benign tumors that arise within the retinal nerve fiber layer. Differential diagnosis constitutes high importance since they may be misdiagnosed as retinoblastoma, and therefore may be overtreated. Whereas retinoblastoma requires immediate treatment, retinal astrocytic hamartomas are commonly followed-up. Multimodal imaging with B-scan ultrasonography and optical coherence tomography are useful in distinguishing those two entities.

Keywords: neoplasms; optical coherence tomography; retinal astrocytic hamartoma; retinal tumors; retinoblastoma.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1. A) Fundus image of the left eye at initial examination shows a well-defined, opaque, minimally calcified, whitish-yellow lesion that is covering the optic disc. B) B-scan ultrasonography image of the left eye at initial examination shows high internal reflectivity, posterior shadowing, and intratumoral cystic spaces.
Figure 2
Figure 2. A) Fundus image of the left eye after a six-year follow-up shows a minimal change. B) Optical coherence tomography image of the left eye after six-year follow-up shows intratumoral cystic spaces and acoustic shadowing due to the calcification.

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