Purpose: To describe and clinically characterize a syndrome of self-inflict
ed scleritis,
Study Design: Case reports and literature review.
Methods: Two patients had persistent scleritis at presentation. Both did no
t respond to prescribed therapy, including systemic corticosteroids and imm
unosuppression, The first had unexplained, diffuse anterior scleritis and p
ersistent linear keratoconjunctival abrasions after a work-related injury.
Several objective indicators pointed to concealed noncompliance with medica
tions. The second patient was a medical assistant with diffuse, unilateral
anterior scleritis and unexplained visual loss. Systemic work-up was negati
ve. She had pharmacologic mydriasis and keratoconjunctival abrasions at pre
sentation.
Results: Systemic therapy was stopped in both patients. The first patient,
who was in the process of requesting permanent disability status, showed pe
rsistent inflammation on each follow-up visit. The second patient improved
with no further therapy after she was confronted with objective indicators
of a self-inflicted condition.
Conclusions: Although the presentation of self-inflicted scleritis can be s
imilar to that of idiopathic or autoimmune anterior scleritis, the former m
ay show additional findings of traumatic conjunctival and corneal abrasions
. Indicators of self-inflicted etiology, of which malingering is one such e
ntity, include evidence of concealed noncompliance with prescribed treatmen
ts and lack of response to potent antiinflammatory and immunosuppressive ag
ents. Correct diagnosis including early psychiatric evaluation in all such
cases, may help prevent unnecessary treatment and unjustified work-related
compensation. Ophthalmology 2001;108:192-195 (C) 2001 by the American Acade
my of Ophthalmology.