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Peer-reviewed veterinary case report

Mixed histiocytic sarcoma causing lameness in Bernese Mountain Dog

By Hickey, Jillian et al.Ā·Published in Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, IncĀ·2025Ā·Wheat Ridge Animal Hospital, United StatesĀ·View original on PubMed →

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Original publication title: Mixed histiocytic sarcoma in a Bernese Mountain Dog.

Species:
dog
Dog limpingStomach & digestionDogs

Plain-English summary

An 8-year-old spayed female Bernese Mountain Dog was brought to the vet because she was limping on her right front leg and had a previous diagnosis of Evans syndrome, which wasn't getting better with treatment. After further tests, the vet suspected a rare type of cancer called mixed histiocytic sarcoma, which affects the immune system and can be difficult to diagnose. An autopsy confirmed the diagnosis, showing cancer in her lungs, spleen, liver, and bone marrow. Unfortunately, the complexity of her condition made treatment challenging, and the outcome was not favorable.

People also search for: Bernese Mountain Dog limping Ā· mixed histiocytic sarcoma in dogs Ā· Evans syndrome treatment in dogs

Abstract

An 8-y-old, spayed female Bernese Mountain Dog was presented to a referral center for evaluation of right thoracic limb lameness and previously suspected Evans syndrome that had been poorly responsive to immunosuppressive therapy. Based on review of examination findings and laboratory data, Evans syndrome was deemed unlikely and hemophagocytic histiocytic sarcoma (HHS) was strongly suspected. On blood smear evaluation, atypical, histiocytic cells were noted, some of which exhibited siderophagia. Considering that circulating cells are not typically observed in dogs with HHS, additional diagnostic investigation was performed. Autopsy and histopathology revealed that the dog had a mixed form of HS (dendritic-cell origin HS in the lung, and HHS in the spleen, liver, and bone marrow), and immunocytochemical characterization of cultured cells derived from blood suggested that the cells were of dendritic HS origin, rather than HHS origin, as originally suspected. Whole-exome sequencing revealed genetic similarity between cell lines derived from lung tissue and blood, providing additional evidence of the relatedness of these 2 cell populations. Our case highlights the rare entity of mixed HS and typifies the inherent challenges in classifying rare, atypical, circulating neoplastic cells.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39866033/