ReviewPediatric radiology2013
Imaging features of medulloepithelioma: report of four cases and review of the literature.
Review in Pediatric radiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.
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Who cites it
7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.
- Practical guidelines on imaging of retinoblastoma: a 2025 update on behalf of the European Retinoblastoma Imaging Collaboration and the European Retinoblastoma Group.European radiology · 2026Guideline
- Ciliary body medulloepithelioma treated with intra-operative brachytherapy after fine needle aspiration biopsy.Journal of contemporary brachytherapy · 2022Article
- Imaging of DICER1 syndrome.Pediatric radiology · 2019Review
- Intraocular medulloepithelioma - A review of clinical features, DICER 1 mutation, and management.Indian journal of ophthalmology · 2019Review
- Intraocular medulloepithelioma in children: clinicopathologic features itself hardly differentiate it from retinoblastoma.International journal of ophthalmology · 2019Article
- Conventional, diffusion, and permeability MR findings in ocular medulloepithelioma.Neuroradiology · 2018Article
- Unusual case of intraocular medulloepithelioma in an adult male.Romanian journal of ophthalmologyArticle
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundIntraocular medulloepithelioma is a childhood tumor arising from the nonpigmented primitive ciliary neuroepithelium. Although rarer than retinoblastoma, it remains the second most common primary intraocular neoplasm in children. The rarity of intraocular medulloepithelioma creates the challenge in establishing a clinical diagnosis, and radiologically the tumor is often confused with other intraocular masses.
objectiveTo describe the clinical, imaging and pathological features of intraocular medulloepithelioma with emphasis on the role of imaging to enable its differentiation from more common intraocular pathology. MATERIALS AND
methodsWe retrospectively analyzed the clinical, histopathological and imaging data of four children with intraocular medulloepithelioma.
resultsAll four children had medulloepithelioma arising from the ciliary body. The children were imaged with US (n = 3), MRI (n = 4), whole-body (99m)Tc-MDP scintigraphy (n = 2) and CT (n = 1). All four children had enucleation of the involved eye. One tumor was a malignant teratoid variant, two tumors were malignant nonteratoid variants and one was a nonteratoid variant of uncertain malignant potential. None of the tumors had extraocular extension on histopathology or imaging. Two children had associated retinal detachment on US and MRI examinations. All tumors were iso/hyperintense to vitreous on T1-weighted and hypointense on T2-weighted MRI and showed marked contrast enhancement of the solid components. No calcifications were identified on US or CT examinations.
conclusionOur findings are consistent with previously reported cases of medulloepithelioma. This series emphasizes the roles of various imaging modalities, with pathological correlation, in differentiating the tumor from other ciliary body masses, in detecting tumor extension and in identifying associated ocular complications. In this series we also describe the results of postsurgical follow-up for tumor recurrence.
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