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 Vé, France·View original on PubMed →
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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 called prednisolone, but it caused severe side effects and the dog's condition worsened when the dose was lowered. The vet then switched to a medication called oclacitinib, which is known to help with autoimmune skin issues. Within a month, the dog's skin had completely healed, and there were no signs of relapse after a year of treatment, with no reported side effects.
People also search for: dog skin blisters treatment · autoimmune skin disease in dogs · oclacitinib for dogs · German shepherd skin problems · prednisolone side effects in dogs
Abstract
BACKGROUND: Autoimmune 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/OBJECTIVES: To evaluate oral oclacitinib, a JAK-1 predominant inhibitor, in one case of ASBD in a dog. CASE REPORT: A 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. CONCLUSION: The 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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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28635010/