“…1 In our case, the sole presence of subepithelial fibrosis and corneal perforation, in the absence of skin or other mucosal lesions, made the diagnosis clinically indistinguishable from other cicatricial conjunctivitis, such as MMP, rosacea, and Stevens–Johnson syndrome (SjS). 5 Recurrent hordeolum and chalazion, lid margin telangiectasia, and erythema are common findings in ocular rosacea. 2 On the other hand, acute sloughing of the entire ocular surface with eyelash loss and symblepharon formation, along with a recent history of systemic drug use, mainly anticonvulsants or antibiotics, are the hallmark of ocular SjS.…”