1. Choroidal Hemangioma in a Black Patient With Sturge-Weber Syndrome: Challenges in Diagnosis
- Author
-
Paul T. Finger, Nitish Mehta, Edmund Tsui, Yasha S. Modi, and Soshian Sarrafpour
- Subjects
Male ,medicine.medical_specialty ,genetic structures ,Adolescent ,Radiography ,Sturge–Weber syndrome ,Black People ,03 medical and health sciences ,0302 clinical medicine ,Vascularity ,Sturge-Weber Syndrome ,Ophthalmology ,medicine ,Humans ,Retina ,business.industry ,Choroid Neoplasms ,Exudative retinal detachment ,Cheek ,medicine.disease ,eye diseases ,medicine.anatomical_structure ,030221 ophthalmology & optometry ,Nevus flammeus ,sense organs ,medicine.symptom ,Choroidal hemangioma ,business ,Hemangioma - Abstract
A black teenager presented with long-standing vision loss in his right eye. Clinical exam revealed increased conjunctival vascularity and total exudative retinal detachment of the right eye. Ultrasound imaging demonstrated a choroidal mass with moderate-to-high reflectivity consistent with a choroidal hemangioma. A closer external examination demonstrated a subtle reddish hue of the eyelids and cheek, consistent with a nevus flammeus. MRI of the brain revealed a T2 enhancing vascular mass. Collectively, these findings were consistent with Sturge-Weber Syndrome. This case highlights the need for a high degree of suspicion for Sturge-Weber Syndrome in dark-skinned individuals that can otherwise mask the nevus flammeus. Physical exam findings and radiographic evidence can be used to guide the diagnosis. [ Ophthalmic Surg Lasers Imaging Retina . 2019;50:183–186.]
- Published
- 2018