SUMMARY A solitary choroidal mass with an overlying neurosensory retinal detachment was seen in an otherwise healthy 25-year-old Caucasian female. Ocular and general physical examinations, serum chemistry, and pathological examination of a lymph node biopsy confirmed sarcoidosis as the cause for the choroidal mass. Treatment with systemic steroids resulted in resolution of the lesion and return of normal visual acuity.
Case reportA 25-year-old Caucasian female was seen by her local ophthalmologist and referred for retinal examination because of central blurring in her left eye for the previous 3 days. The patient noticed no redness, pain, or photophobia. Ocular history revealed one sister who was noted to have a unilateral eye defect which by history was suggestive of a coloboma. The sister was not examined. Past medical history was negative except for an upper respiratory infection one month prior to ocular examination. Four months previously the patient had given birth to a full-term, healthy child, delivered by caesarean section because of prolonged labour. After delivery the patient had a raised white blood count, the cause of which was never determined. There was no history of fever, weight loss, or anorexia. The patient abused neither drugs nor alcohol.Ocular examination revealed best corrected visual acuity of 20/20 OD, 20/100 OS. Applanation intraocular tensions were 12/13. External examination was normal. The pupils were 4 mm, equal, round, and reacted to light directly and consensually without an afferent defect. A muscle balance test showed orthophoria. Motility tests revealed full ductions and versions. A photo stress test showed a delay on the left greater than one minute compared with the right. American Optical colour plates showed 12 of 15 correct OD, 0 of 15 OS. An Amsler grid test showed a central scotoma OS. Slit-lamp examination of the anterior segment was unremarkable in both eyes.