We report a calcified cataractous lens in a 24-year-old man who had retinal degeneration in the right eye since childhood. The visual acuity had dropped to light perception. Clear corneal phacoemulsification was performed, and the shell of a 5.4 mm x 4.0 mm x 2.0 mm calcified substance was removed with a forceps using the can-opener technique. The specimen was analyzed using radiological study, histopathological examination, chemical element analysis, and transmission electron microscopy. Four years postoperatively, the patient's visual acuity was 20/200.

Adult-onset Still's disease is a multisystem inflammatory disorder of unknown etiology and is characterized by high, spiking fever, arthritis, evanescent maculopapular rash, myalgia, serositis, leukocytosis, and involvement of various organs including the eyes. The ocular manifestations have been described including orbital pseudotumor, ptosis, and diplopia with orbital pain but never Purtscher's-like retinopathy. We describe a 21-year-old male patient with adult-onset Still's disease who developed the Purtscher's-like retinopathy. To our knowledge, this is the first reported adult-onset Still's disease patient with Purtscher's-like retinopathy as the initial presentation.

Purpose: We report a rare case of complete anterior dislocation of the capsular tension ring (CTR)-intraocular lens (IOL) complex spontaneously.Methods: Case report. Results:The patient was initially treated conservatively because she was unwilling to receive operation. However, surgical treatment was eventually performed when the implant attached to her cornea and caused endothelial decompensation. From an outpatient department review several months later, it was found that her corneal edema and visual acuity improved. Conclusion:The possibility of CTR-IOL anterior dislocation should be mentioned to the patient before mydriatic examination. Surgical options should be taken early especially once complications such as uveitis, glaucoma, macular edema and corneal endothelium decompensation happen.

A 30 year old female with absolute glaucoma status post-evisceration developed recurrent orbital implant exposure and scleral melting. We successfully treated the large conjunctiva defect by utilizing secondary implant of dermis fat graft for tissue growth and tension-free conjunctiva closure. The patient was satisfied with the postoperative outcome, and no major complications were observed in the following six months. Age and underlying disease may both be associated with dermis fat graft properties. Our case demonstrates that secondary dermis fat implantation is an effective method for treatment of exposed orbital implants and empty sockets after extrusion of an orbital implant.