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Orbital compression syndrome in a Ugandan child with sickle cell disease: A case report
Ronald Olum1, Catherine Nabaggala2, Victoria Katasi Mwebe3
1School of Medicine Makerere University College of Health Sciences Kampala Uganda.
Abstract:
Orbital compression syndrome is a rare acute complication of sickle cell disease that may impair vision. Assessment by a multidisciplinary team incorporates detailed history and physical examination, fundoscopy, and appropriate imaging to exclude infections or neoplasms. Supportive treatment is adequate unless there is evidence of life-threatening space-occupying lesion warranting surgery.
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