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Peer-reviewed veterinary case report

Dog with autoimmune blistering skin disease treated with oclacitinib

By Aymeric, Estelle & Bensignor, Emmanuel·Published in Veterinary Dermatology·2017·Clinique Vétérinaire Avenue 19 mars 1962 13390 Auriol France, France·View original on Crossref

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Original publication title: A case of presumed autoimmune subepidermal blistering dermatosis treated with oclacitinib

Species:
dog

Plain-English summary

A 5-year-old German shepherd mix was brought in with painful, blistering skin lesions on its face, mouth, and body. The vet initially treated the dog with a steroid medication, but it caused severe side effects and the skin condition returned when the dose was lowered. The vet then switched to oclacitinib, a newer medication, which led to complete healing of the skin within a month, and the dog remained symptom-free for a year without any side effects. This case suggests that oclacitinib could be a promising option for treating certain autoimmune skin issues in dogs.

People also search for: dog skin blisters treatment · autoimmune skin disease in dogs · oclacitinib for dogs · German shepherd skin problems · dog steroid side effects

Abstract

BackgroundAutoimmune subepidermal blistering dermatoses (ASBD) are a group of severe autoimmune dermatoses rarely described in dogs. Their treatment usually necessitates the long term use of medications potentially associated with adverse effects. In humans, Janus Kinase (JAK) inhibitors have been demonstrated to be of value in some cases of autoimmune skin disease.Hypothesis/ObjectivesTo evaluate oral oclacitinib, a JAK‐1 predominant inhibitor, in one case of ASBD in a dog.Case reportA 5‐year‐old German shepherd cross‐bred dog was presented with an acute onset of ulcerative and blistering skin lesions on the face, oral cavity, lateral trunk and limbs. Associated systemic signs were not seen. A clinical diagnosis of ASBD was supported by the finding of subepidermal clefts and visualization of the epidermal basement membrane zone at the bottom of the clefts on histopathological examination. Treatment was initiated with prednisolone at 1.2 mg/kg twice daily. Because of severe adverse effects and relapse, when the prednisolone dose was reduced, oclacitinib therapy was administered at 0.5 mg/kg twice a day. A complete resolution of clinical signs was noted after one month and no relapse was observed after twelve months of treatment. No adverse effects were reported.ConclusionThe use of oclacitinib may be useful for the treatment of some autoimmune skin diseases in dogs. Further controlled studies are needed to confirm our findings.

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Original publication on Crossref: https://doi.org/10.1111/vde.12458