ABSTRACT
An 8-year-old domestic shorthair cat was examined for severe anterior uveitis of the right eye that was unresponsive to aggressive treatment with anti-inflammatory drugs and for a possible intraocular parasite or foreign body trapped within a large fibrin clot in the anterior chamber. Surgical exploration of a presumed entry site on the caudal aspect of the third eyelid led to keratotomy and removal of a larval parasite later identified as a first instar Cuterebra spp. Aggressive treatment with anti-inflammatory drugs was continued after surgery, and intraocular pressure was monitored closely to ensure that the cat did not develop glaucoma. Two weeks after surgery, the cat had vision in the affected eye, with resolving uveitis and a normal fundus. Six weeks after surgery, the uveitis continued to resolve; however, the cat did not have vision in the affected eye, and examination of the fundus revealed retinal atrophy. In contrast to the condition in humans, a Cuterebra spp larval infection within the eye of cats may cause not only an intense, acute inflammatory reaction, but also retinal degeneration and blindness despite prompt surgical removal.
Subject(s)
Cat Diseases/parasitology , Diptera/classification , Eye Infections, Parasitic/veterinary , Myiasis/veterinary , Uveitis, Anterior/veterinary , Animals , Cat Diseases/therapy , Cats , Diagnosis, Differential , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/therapy , Female , Larva , Myiasis/parasitology , Myiasis/therapy , Uveitis, Anterior/parasitology , Uveitis, Anterior/therapyABSTRACT
The clinical and pathologic features of six cases of atypical primary ocular melanoma in cats are described. In contrast to diffuse iris melanomas, these atypical tumors originated multifocally from any portion of the uvea and in five of the six cases were very advanced at the time of clinical presentation. Two of the advanced cases involved primarily the ciliary body, while three others showed extensive involvement of the choroid. Histologically, these tumors consisted primarily of round, heavily pigmented cells lacking the anaplastic nuclear features characteristic of advanced diffuse iris melanomas. The advanced stage of the tumors at presentation may have been due to either the posterior uveal origin of these tumors or to more rapid progression. Additional cases with long-term follow-up need to be studied in order to accurately assess the biological behaviour of these tumors.
