“…Immune‐mediated keratitis was diagnosed based on criteria described previously . Briefly, IMMK was characterized by corneal opacification localized to the superficial stromal, middle stroma, or endothelium; corneal vascularization; mild or lack of ocular pain; no etiologic organisms identified; and favorable response to immunosuppressive therapy . Pigmentary keratouveitis (PK), a disease that is similar to IMMK, was diagnosed based on clinical criteria described recently, which included signs of corneal edema, pigmented keratic precipitates, anterior uveitis, and iridal depigmentation .…”