Evidence map›Paper›PMID 40041068›Full record

ArticleSurgical neurology international2025

Orbital tumors: A retrospective analysis of cases from Iraq and orbital anatomical perspectives.

Najah K Mohammad

Abstract read
In one paragraph

Article in Surgical neurology international, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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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

1 author.

Najah K MohammadDepartment of Surgery, University of Baghdad, College of Medicine, Baghdad, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: With its vital ocular and adnexal structures, the orbit may be affected by a wide array of neoplasms, including primary, secondary, and metastatic neoplasms. These lesions pose significant diagnostic and therapeutic challenges in view of complex orbital anatomy and overlapping clinical presentations. This study aimed to analyze the epidemiology, clinical features, refractive impacts, and management outcomes of orbital tumors, providing insights to optimize diagnosis and treatment strategies. Methods: This study retrospectively analyzes 22 patients who had a presentation of orbital tumors at the Istishari Ophthalmic Eye Hospital between January 2019 and January 2024. Collected data were demographic, clinical, refractive, tumor type, laterality, and management outcome. Advanced imaging studies and histopathological diagnoses confirm the diagnoses. Statistical tests will be applied in assessing the relationship among tumor types, clinical presentations, and refractive changes by means of Analysis of Variance and Chi-square tests. Results: Cavernous hemangioma was the most prevalent tumor (54.5%), followed by adenoid cystic carcinoma and optic nerve meningioma (13.6% and 9.1%, respectively). Proptosis (31.8%) was the predominant symptom. Significant refractive changes were noted across tumor types ( Conclusion: Orbital tumors present diverse clinical and refractive manifestations, necessitating individualized, multidisciplinary approaches for effective management. This study underscores the importance of advanced imaging, tailored surgical strategies, and the integration of minimally invasive techniques. Future multicenter studies are needed to validate these findings and enhance therapeutic outcomes.

Indexed as

Lateral orbitotomyMultidisciplinary managementOrbital tumorsProptosisRefractive changes

Identifiers

PMID40041068
PMCPMC11878717

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Registered trials

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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.