Peer-reviewed veterinary case report
Rottweiler puppy with skin nodules from Caryospora infection
By Tham, Heng L et al.·Published in Veterinary dermatology·2016·Department of Clinical Sciences, United States·View original on PubMed →
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Original publication title: Protozoal nodular dermatitis and panniculitis in a Rottweiler puppy caused by Caryospora bigenetica.
- Species:
- dog
Plain-English summary
A Rottweiler puppy developed skin problems, showing multiple lumps under the skin that were up to 2 cm wide. Tests confirmed the puppy was infected with a rare parasite called Caryospora bigenetica. The vet treated the puppy with a combination of medications, including trimethoprim-sulfamethoxazole and clindamycin, which cleared up the lumps in about six weeks. However, after stopping the treatment, the lumps returned quickly, and the puppy needed to go back on the medications to resolve the issue again. While the puppy had some periods of remission, managing this infection proved to be challenging due to relapses.
People also search for: Rottweiler puppy skin lumps · Caryospora bigenetica treatment · dog skin infection medication
Abstract
BACKGROUND: Caryospora bigenetica is an intracellular protozoan parasite in snakes and raptors (primary hosts) and rodents (secondary host). Experimental infection has been documented in mice, pigs and goats; natural infection in dogs is rare. OBJECTIVES: To describe the clinical presentation, histological features, treatment and outcome of a case of protozoal nodular dermatitis and panniculitis in a Rottweiler puppy caused by C. bigenetica. RESULTS: The puppy presented with generalized subcutaneous nodules measuring up to 2 cm in diameter. Histopathology revealed marked suppurative to pyogranulomatous dermatitis and panniculitis with intralesional protozoal organism. PCR and DNA sequencing confirmed infection with C. bigenetica. Treatment with a combination of oral trimethoprim-sulfamethoxazole (TMS), pyrimethamine and high-dose clindamycin (20 mg/kg twice daily) resulted in resolution of lesions in 6 weeks. Discontinuation of the treatment 2 weeks later was followed by a rapid relapse of skin lesions. Clindamycin and TMS were restarted and all lesions resolved within 2 weeks; TMS was discontinued 4 weeks later due to adverse effects. The lesions remained in remission for 2 months while the puppy received clindamycin monotherapy before a second relapse of skin lesions occurred. CONCLUSION AND CLINICAL IMPORTANCE: To the best of the authors' knowledge, this is the first documentation of the treatment and outcome of C. bigenetica cutaneous infection in a dog. Although remission of clinical signs can be achieved with combination therapy of clindamycin and TMS, long-term management is challenging and relapses should be anticipated.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/26567903/