Corneal dystrophies are usually bilateral. We report a case of unilateral map-dot corneal dystrophy.

Molluscum contagiosum should be included in the differential diagnosis of chronic follicular conjunctivitis. A complete eye examination is essential to decide the proper treatment for any type of conjunctivitis.

20200725;This is the case of a 36-year-old white female with an iris nevus that progressed to diffuse iris melanoma in just 4 months. Management included fine-needle aspiration biopsy and Iodine-125 plaque radiotherapy.

A case of bilateral acute annular outer retinopathy in a 52 year old man who presented with decreased vision and bilateral central scotomas

Congenital RPE hamartoma almost always manifests in the macula, rarely affects visual acuity unless located directly in the foveola, and has not been reported to enlarge or undergo malignant transformation.

A 50-year-old woman presented with long-standing left corneal opacity resulting in diminished visual acuity. B Optical coherence tomography revealed focal hyperreflectivity in the mid and deep corneal stroma, corresponding to the lipid deposits seen clinically, with sparing of the epithelium and anterior stroma. A penetrating keratoplasty was performed. C Hematoxylin and eosin staining demonstrated focal pronounced mid and deep stromal neovascularization, scarring and foamy cells the anterior stroma was spared x20. D Immunostaining for adipophilin accentuated the numerous foamy cells, highlighting lipid-containing vesicles x60 and inset.

We find this case to be interesting for a several reasons. First, the presentation of solitary metastasis to the anterior chamber angle secondary to prostate adenocarcinoma is highly unusual. Second, from a management standpoint, this patient did not require invasive intraocular biopsy in order to establish diagnosis. Third, the ocular metastasis responded completely to androgen deprivation therapy rather than the conventional radiotherapy techniques frequently used to treat intraocular tumors and his vision was fully restored. Finally, this case required collaboration between a large number of subspecialty services, and consequently we feel it will appeal to a wide audience.

Retinochoroidal ColobomaRCC is a developmental anomaly that occurs due to failed or incomplete closure of the embryonic fissure. Associated complications include Pre-senile cataract , Retinal detachment, and rarely Choroidal neovascularisationCNV. Prophylactic Barrage laser around the coloboma helps in prevention of retinal detachment in these eyes. CNV in these eyes have been reported to respond well to Ant-VEGF therapy.

Blunt ocular trauma produces an isolated complete 360-degree iridodialysis with preservation of the remaining intraocular structures.

The image reveals the classic, eye-catching appearance of lattice corneal dystrophy. It is a localized form of a disease that results from the deposition of misfolded proteins in the cornea, leading to progressive loss of vision among other symptoms.