J Korean Ophthalmol Soc > Volume 50(2); 2009 > Article
Journal of the Korean Ophthalmological Society 2009;50(2):294-298.
DOI: https://doi.org/10.3341/jkos.2009.50.2.294    Published online February 15, 2009.
Orbital Leiomyoma: A Case Report.
Jongshin Kim, Nam Ju Kim
1Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Korea. resourceful@hanmail.net
2Department of Ophthalmology, Seoul National University Bundang Hospital, Gyeonggi, Korea.
안와 평활근종 1예
김종신1ㆍ김남주1,2
Department of Ophthalmology, Seoul National University College of Medicine1, Seoul, Korea / Department of Ophthalmology, Seoul National University Bundang Hospital2, Gyeonggi, Korea
Abstract
PURPOSE
To report a case of orbital leiomyoma presenting with proptosis. CASE SUMMARY: A 69-year-old woman presented with a 3-month history of proptosis in her left eye. Intraocular pressure was 17 mmHg in her right eye and 23 mmHg in her left eye. There was a left hypotropia on upgaze. A fundus examination showed retinal folds in the superotemporal area in her left eye. Computed tomography revealed a 2.6 cm-sized well-defined enhancing solid mass in the superotemporal extraconal space of the left orbit, pushing her left eye forward. Lateral orbitotomy, tumor removal, and biopsy were performed. Pathological findings showed a fascicular pattern of benign spindle cells with mild cellular pleomorphism and hyaline degeneration, without mitotic figures. Immunohistochemical stain was positive with smooth muscle actin (SMA), which was compatible with orbital leiomyoma. CONCLUSIONS: Orbital leiomyoma is rare, but it should be considered as a differential diagnosis of orbital tumor when the presenting symptom is proptosis and limitation of ocular movement.
Key Words: Orbital leiomyoma;Orbital tumor;Proptosis


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