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CASE REPORT
Year : 2018  |  Volume : 8  |  Issue : 3  |  Page : 110-113

Aggressive orbital rhabdomyosarcoma in adulthood: A case report in a public hospital in Damascus, Syria


1 Department of Internal Medicine, Tishreen hospital, Damascus, Syria
2 Department of Internal Medicine, Al Assad University Hospital and Al Mouwasat University Hospital, Damascus, Syria
3 Department of Internal Medicine, University of Jordan, Amman, Jordan
4 Department of Ophthalmology, Yusuf Al-Azma Hospital, Damascus, Syria

Correspondence Address:
Dr. Hasan Nabil Al Houri
Department of Internal Medicine, Al Assad University Hospital and Al Mouwasat University Hospital, Damascus
Syria
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ajm.AJM_62_18

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Orbital rhabdomyosarcoma (RMS) is a highly malignant tumor that originates mainly from mesenchymal tissue. It is considered a rare childhood malignancy; therefore, presentation in adulthood is scarce. In this case report, a 36-year-old male patient presented with a rapidly progressive RMS of the left orbit. The patient was treated in a different institution with radiochemotherapy with good response. However, relapse occurred after 2 months of completing the course, as rapid growing proptosis. Computed tomography scan revealed a lesion in the left orbit with invasion of the left ethmoid cells and the left maxillary sinus. Exenteration of the left orbit with the left partial maxillectomy and ethmoidectomy was performed. RMS is a highly aggressive malignancy that should be considered in any orbital mass that progresses rapidly. Surgery should be the first line in treatment. Delay in diagnosis and inappropriate treatment negatively affects the outcome.


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