Evidence map›Paper›PMID 30510760›Full record

ArticleAnnals of medicine and surgery (2012)2018

Epibulbar complex and osseous choristoma: Clinicopathological study with interesting associations.

Mohammed M Aldossary, Hind M Alkatan, Azza My Maktabi

Abstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

9 citing papers in PubMed.

  1. Article
  2. Epibulbar osseous choristoma.BMC ophthalmology · 2025
    Article
  3. Article
  4. Article
  5. Epibulbar osseous choristoma: a case report.Journal of surgical case reports · 2023
    Article
  6. Epibulbar osseous choristoma: Two case reports.World journal of clinical cases · 2022
    Article
  7. Article
  8. Lacrimal gland choristomas.Arquivos brasileiros de oftalmologia · 2021
    Review
  9. Isolated eyelid coloboma in association with complex choristoma in a newborn: A case report.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
    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

3 authors.

Mohammed M AldossaryOphthalmology Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Hind M AlkatanDepartments of Ophthalmology & Pathology, King Saud University, Riyadh, Saudi Arabia.
Azza My MaktabiPathology & Laboratory Medicine Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MATERIALS AND

methodsA retrospective cohort study of cases with tissue diagnosis of epibulbar choristoma in 2 centers presenting during the period: 2000-2016 with focus on cases of complex and osseous choristoma. Demographic and clinical data were collected by the resident from medical records. The histopathological slides were reviewed by 2 pathologists and cases of complex and osseous choristoma were analyzed by biostatical staff.

results120 epibulbar choristomas were identified. 13/120 patients (10.8%) with complex choristoma and 2/120 patients (1.7%) with osseous choristoma. 15 cases were further analyzed: 7 were males and 8 were females. Mean age at presentation was 7.6 year. Commonest location was temporal in 66.6%. The presence of smooth muscle component was associated with a larger size choristoma (p = 0.042). 73.3% had other ophthalmic manifestations (mostly eyelid anomalies) while 9 systemic associations (mostly Goldenhar's syndrome) were found in 8/13 cases of complex choristoma.

conclusionEpibulbar complex and osseous choristomas are rare. Histopathologically, the presence of smooth muscle significantly correlates with the lesion size. Complex choristoma is more likely to be associated with systemic manifestations. Further genetic studies for this condition are recommended.

Identifiers

PMID30510760
PMCPMC6258243

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