Bilateral Subperiosteal Hematoma and Orbital Compression Syndrome in Sickle Cell Disease
| Autor: | Selma Unal, Özer Dursun, Cem Sundu, Erdem Dinç, Ayça Sari |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
Male
medicine.medical_specialty Adolescent genetic structures Exophthalmos Infarction Anemia Sickle Cell 03 medical and health sciences 0302 clinical medicine Hematoma Orbital Diseases medicine Humans medicine.diagnostic_test business.industry Magnetic resonance imaging General Medicine medicine.disease Magnetic Resonance Imaging eye diseases Surgery Posterior segment of eyeball Otorhinolaryngology Methylprednisolone Cellulitis 030221 ophthalmology & optometry sense organs medicine.symptom business Orbit 030217 neurology & neurosurgery medicine.drug |
| Zdroj: | Journal of Craniofacial Surgery. 28:e775-e776 |
| ISSN: | 1049-2275 |
| DOI: | 10.1097/scs.0000000000003972 |
| Popis: | A 14-year-old boy with sickle cell disease presented with preseptal cellulitis findings as proptosis, eyelid edema, and hyperemia. His best corrected visual acuity in the right eye was 20/20 and 16/20 in the left eye. He had limited ductions in vertical and lateral gazes in both eyes. Bilateral venous tortuosity was observed in posterior segment examination. Orbital bone infarction and subperiosteal hematoma were seen in magnetic resonance imaging. He was diagnosed as having orbital compression syndrome secondary to vaso-occlusive crisis of sickle cell disease and was treated with intravenous ampicilin-sulbactam and methylprednisolone. |
| Databáze: | OpenAIRE |
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