Evidence map›Paper›PMID 40534812›Full record

ArticleInternational journal of ophthalmology2025

Dysplasia of extraocular muscles presenting as orbital space-occupying lesions-an extremely rare disorder.

Shi-Yu Tang, Xiang-Jun Wang, Meng-Ya Han, Jian-Hua Yan

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Article in International journal of ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shi-Yu TangState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou 510060, Guangdong Province, China.
Xiang-Jun WangState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou 510060, Guangdong Province, China.
Meng-Ya HanState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou 510060, Guangdong Province, China.
Jian-Hua YanState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou 510060, Guangdong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo describe the clinical manifestations, imaging features and surgical treatments in 5 cases of extraocular muscle (EOM) dysplasia presenting as orbital space-occupying lesions (SOL).

methodsRecords from the 5 cases with EOM dysplasia between 2004 and 2016 were retrospectively reviewed and clinical data were recorded including family history, age at onset, age at surgery, visual acuity, cycloplegic refraction, ocular alignment and motility, stereoacuity, exophthalmos, anterior segment and fundus, orbital computed tomography (CT) or magnetic resonance imaging (MRI) scan, surgical methods and final outcomes.

resultsAll 5 cases (1 male, 4 females) were unilateral (3 right, 2 left eyes). The average age was 5.4y (range 4-6y) with no family history. Patients had unilateral strabismus (horizontal and vertical), restricted eye movement, and eyelid changes (abnormal fissures, lagophthalmos, and/or entropion) in the affected eye. None had proptosis; 1 had 2-mm enophthalmos. Orbital CT/MRI showed irregular, ill-defined masses in EOM. Two anterior orbitotomies and 3 strabismus surgeries were performed, and pathology confirmed EOM dysplasia. After surgery, horizontal deviations, which ranged from exotropia (XT) 10 prism diopter (PD) to esotropia (ET) 10 PD (average 6 PD), decreased by an average of 18 PD, while vertical deviations, which ranged from 4 PD to 20 PD (mean 9.8 PD), decreased by an average of 23.2 PD.

conclusionSOL from EOM dysplasia is non-familial and typically presenting unilaterally characterized by an irregular, diffusely infiltrating mass within the EOM. EOM involvement causes strabismus, restricted eye movement, eyelid changes, and enophthalmos likely due to cicatricial processes.

Indexed as

dysplasiaextraocular muscleorbitspace-occupying lesionstrabismus

Identifiers

PMID40534812
PMCPMC12120459

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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.