Evidence map›Paper›PMID 31124483›Full record

ReviewIndian journal of ophthalmology2019

Intraocular medulloepithelioma - A review of clinical features, DICER 1 mutation, and management.

Sameeksha H Tadepalli, Carol L Shields, Jerry A Shields, Santosh G Honavar

Open access · diamondAbstract readReview
In one paragraph

Review in Indian journal of ophthalmology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Guideline
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  11. Review
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  16. Article
  17. Article
  18. Article
  19. Optic disc and peripapillary tumors.Taiwan journal of ophthalmology
    Review
  20. Ciliary Body Leiomyoma.Case reports in ophthalmology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Sameeksha H TadepalliDepartment of Ocular Oncology, Wills Eye Hospital, Philadelphia, PA, USA; Department of Ocular Oncology, Centre for Sight, Hyderabad, Telangana, India.
Carol L ShieldsDepartment of Ocular Oncology, Wills Eye Hospital, Philadelphia, PA, USA, India.
Jerry A ShieldsDepartment of Ocular Oncology, Wills Eye Hospital, Philadelphia, PA, USA, India.
Santosh G HonavarDepartment of Ocular Oncology, Centre for Sight, Hyderabad, Telangana, India.
Wills Eye Hospital · USCentre for Sight · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intraocular medulloepithelioma is a nonhereditary neoplasm of childhood arising from primitive medullary epithelium. It most often involves the ciliary body. Most patients present between 2 and 10 years of age with loss of vision, pain, leucocoria, or conjunctival congestion. The mass appears as a grey-white ciliary body lesion with intratumoral cysts. Presence of a neoplastic cyclitic membrane with extension to retrolental region is characteristic. Secondary manifestations like cataract and neovascular glaucoma may be present in up to 50% and 60% patients, respectively. These could be the first signs for which, unfortunately, about 50% patients undergo surgery before recognition of the hidden tumor. Systemic correlation with pleuropulmonary blastoma (DICER1 gene) has been documented in 5% cases. Histopathology shows primitive neuroepithelial cells arranged as cords closely resembling the primitive retina. Histopathologically, the tumor is classified as teratoid (containing heteroplastic elements) and nonteratoid (containing medullary epithelial elements), each of which are further subclassified as benign or malignant. Retinoblastoma-like and sarcoma-like areas may be seen within the tissue. The treatment modality depends on tumor size and extent of invasion. For small localized tumors (≤3-4 clock hours), conservative treatments with cryotherapy, plaque radiotherapy, or partial lamellar sclerouvectomy (PLSU) have been used. Plaque brachytherapy is generally preferred for best tumor control. Advanced and extensive tumors require enucleation. Rare use of intra-arterial and intravitreal chemotherapy has been employed. Systemic prognosis is favorable, but those with extraocular extension and orbital involvement show risk for local recurrence and metastatic disease, which can lead to death.

Indexed as

Disease ManagementEye NeoplasmsMutationNeuroectodermal Tumors, PrimitiveCombined Modality TherapyDEAD-box RNA HelicasesDNA, NeoplasmHumansRibonuclease IIIDEAD-box RNA HelicasesDICER1 protein, humanDNA, NeoplasmRibonuclease IIIciliary bodyCiliary epitheliumdiktyomamedulloepitheliomanon-teratoidteratoidtumor

Identifiers

PMID31124483
PMCPMC6552580
OpenAlexW2947390990

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.