Background Cerebrospinal fluid (CSF) analysis is an important component of the evaluation of horses with neurologic disease. Lumbosacral (LS) centesis is routine, but CSF is also collected from the space between the first and second cervical vertebrae (C1‐C2). Objectives To compare collection times, CSF cytology results, and equine protozoal myelitis (EPM) titers of CSF collected from the C1‐C2 and LS sites. Animals Fifteen university‐owned adult horses with no evidence of neurologic disease, and 9 horses with signs of neurologic disease: 3 university‐owned and 6 client‐owned. Methods Prospective study. Cerebrospinal fluid collection from the LS space and C1‐C2 space of each horse was performed in randomized order. Continuous data were analyzed using mixed‐effects linear models and count data using mixed‐effects negative binomial regression. Statistical significance was set at P < .05. Results Cerebrospinal fluid collected from the C1‐C2 site had a significantly lower mean protein concentration (49 [95% CI: 43‐55.8] mg/dL C1‐C2 versus 52.1 [95% CI: 45.7‐59.3] mg/dL LS; P = .03) and red blood cell count (6 [95% CI: 2‐16] cells/μL versus 33 [95% CI: 13‐81] cells/μL; P = .02). Collection time, total nucleated cell count, EPM titers, and serum:CSF EPM titer ratios were not significantly different between collection sites. Conclusions and Clinical Importance Cerebrospinal fluid from the C1‐C2 space provides an acceptable alternative to LS CSF collection with decreased likelihood of clinically important blood contamination of samples.

An 8-y-old Labrador Retriever was presented to a small animal practice in northern Virginia with a history of recent lethargy. Physical examination findings were unremarkable. Ultrasound revealed several large hepatic masses and multiple smaller masses involving the pancreas. Cytologic findings on fine-needle aspirates of the hepatic masses included inflammation and necrosis with eosinophilic, membranous oval structures consistent with cestode infection. Histopathologic findings for biopsies of these masses included extensive necrosis, inflammation, and PAS-positive hyaline-like membranous material interpreted as metacestode cyst wall. A PCR product was generated from aspirate material using primers specific for Echinococcus multilocularis. Subsequent sequence data were 100% homologous to E. multilocularis NADH dehydrogenase subunit I gene sequences. The dog received daily oral albendazole (10 mg/kg) treatment, but its condition deteriorated, and the dog was euthanized. The dog, born in Mississippi, was brought as a puppy to Virginia with no other travel history. To our knowledge, alveolar echinococcosis has not been reported previously in a dog in the United States; E. multilocularis infection was apparently acquired in the mid-Atlantic region of the United States.