A case of sickle cell hemoglobinopathy diagnosed after traumatic hyphema
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Case Report
P: 315-317
December 2005

A case of sickle cell hemoglobinopathy diagnosed after traumatic hyphema

Gulhane Med J 2005;47(4):315-317
1. Diyarbakır Asker Hastanesi Göz Hastalıkları Servisi
2. GATA Haydarpaşa Eğitim Hastanesi Göz Hastalıkları Servisi
3. Eskişehir Hava Hastanesi Göz Hastalıkları Servisi
No information available.
No information available
Received Date: 17.06.2005
Accepted Date: 30.09.2005
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ABSTRACT

Hyphema is traditionally considered as a benign condition by ophthalmologists and expected to disappear within a few days. However, hyphema developing after blunt trauma may be potentially sightthreatening in some cases. Vision-threatening complications of traumatic hyphema are well known in blacks and children with hemoglobinopathy. This report describes a previously healthy case who had marked elevation of intraocular pressure due to a minimal hyphema resulting from blunt trauma, and we emphasize that sickle cell trait hemoglobinopathy should be considered in the differential diagnosis of traumatic hyphema in also white adults.

Keywords:
Sickle cell trait hemoglobinopathy, secondary glaucoma, traumatic hyphema