Peer-reviewed veterinary case report
Cat with progressive histiocytosis nodules goes into remission
By de Sena, Bruna Voltolin et al.·Published in Frontiers in veterinary science·2024·Department of Veterinary Medicine and Surgery, Brazil·View original on PubMed →
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Original publication title: Case report: Complete clinical remission of feline progressive histiocytosis after multimodal treatment including electrochemotherapy.
- Species:
- cat
Plain-English summary
A 6-year-old mixed-breed cat had a nodule on her nose for 9 months, which turned out to be a type of skin cancer called feline progressive histiocytosis. She developed more nodules on her lip, toe, and tail, and initial treatments with chemotherapy didn't work. After trying a combination of treatments including electrochemotherapy and another medication, all the nodules completely disappeared. The cat lived for another 460 days without any signs of the disease returning, showing that this treatment approach was effective.
People also search for: cat skin cancer treatment · feline progressive histiocytosis · electrochemotherapy for cats
Abstract
Feline histiocytic diseases are uncommon and rarely reported. Feline progressive histiocytosis (FPH) is the most common histiocytic disease in cats, predominantly affecting middle-aged animals. The most common presentation is the cutaneous form with solitary or multiple cutaneous nodules. A female, mixed-breed 6-year-old cat was presented with a 9-month history of a nodule in the nasal planum and was diagnosed by histopathology with histiocytic proliferation. At the time of diagnosis, new nodules were discovered on the lower lip, digit, and two lesions in the tail region, with the largest measuring 1.5 cm. Supplementary immunohistochemistry, showed immunolabeling for Iba-1 that in combination with the clinical course of the disease, confirmed the diagnosis of FPH. No response to chemotherapy treatment with lomustine alternated with doxorubicin was achieved. Toceranib phosphate resulted in a transient response and, stable disease for a short period (6 weeks). Electrochemotherapy with bleomycin was initiated and resulted in partial remission. Later on, chlorambucil was also started. Ultimately, the combination of all three treatments led to a complete response and disappearance of all the lesions. FPH is considered a disease resistant to various treatments, and effective treatments have not been reported. In this case report, we describe a successful multimodal therapeutic approach that resulted in complete resolution of the FPH and long-term survival (460 days without external lesions at the time of death). Further studies are necessary to confirm the efficacy of this therapeutic approach.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39239387/