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Peer-reviewed veterinary case report

Cat with progressive histiocytosis nodules goes into remission

By Bruna Voltolin de Sena et al.·Published in Frontiers in Veterinary Science·2024·Department of Veterinary Medicine and Surgery, Veterinary School, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil, CH·View original on DOAJ

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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 was brought in with a 9-month history of nodules on her nose, lip, and tail, which were diagnosed as feline progressive histiocytosis (FPH), a rare skin disease. After trying chemotherapy with no success, the cat received a combination of treatments including electrochemotherapy, which initially led to partial improvement, followed by chlorambucil. Ultimately, this combination of treatments resulted in complete disappearance of all lesions. The cat lived for 460 days without any new skin problems after treatment.

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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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Original publication on DOAJ: https://doi.org/10.3389/fvets.2024.1397592