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dc.contributor.authorKaye, Sarrah
dc.date.accessioned2012-05-25T16:16:57Z
dc.date.available2012-05-25T16:16:57Z
dc.date.issued2012-04-18
dc.identifier.urihttps://hdl.handle.net/1813/28967
dc.description.abstractAn 18 month old female spayed domestic ferret presented to the Cornell University Hospital for Animals for a blood transfusion, following a one-month history of non-regenerative anemia of unknown origin. Bone marrow aspirate cytologic evaluation was diagnostic for pure red cell aplasia, a presumptively immune-mediated disease targeting erythrocyte precursors. This disorder has been reported once previously in the ferret (Malka et al, 2010). The patient initially responded to immunosuppressive therapy with glucocorticoids (2 mg/kg) and cyclosporine (4 mg/kg). Cyclosproine levels one month after initiation were at toxic levels (<2100ng/ml); soon after, the patient developed severe hepatobiliary disease, refractory to treatment. The patient was euthanized 139 days post initial presentation. Post-mortem histological exmaination of the liver revealed biliary coccidiosis with Eimeria spp, a presumptively opportunisitc pathogen that has never been previously reported in adult ferrets.en_US
dc.language.isoen_USen_US
dc.relation.ispartofseriesSenior seminar paper
dc.relation.ispartofseriesSeminar SF610.1 2012
dc.subjectFerrets -- Diseases -- Case studiesen_US
dc.titlePure red cell aplasia in a young ferreten_US
dc.typeterm paperen_US


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