The jejunal lymph nodes of 57 dogs without clinical signs of gastrointestinal disease were examined to characterize their ultrasonographic appearance on B-mode and power Doppler examination, and to obtain ultrasonographic measurements. The lymph nodes were mildly hypoechoic to the mesentery in 71% of dogs and isoechoic in 29%. All dogs, 6 years of age or older had jejunal lymph nodes of uniform echogenicity. In dogs less than 6 years of age, nonuniform lymph nodes with different echopatterns were observed. Although most lymph nodes had no blood flow based on power Doppler examination, hilar blood flow was detected in 33% of dogs, which were generally less than 2 years of age. The median maximum thickness of the jejunal lymph nodes was 3.9 mm (range 1.6-8.2 mm), and their median maximum width 7.5 mm (range 2.6-14.7 mm). There was a significant correlation between larger lymph node diameter and younger age and higher body weight. We concluded that patient age should be considered when interpreting the echopattern and vascularity of jejunal lymph nodes in dogs, and that the jejunal lymph nodes of dogs without clinical signs of gastrointestinal disease may exceed the previously stated upper limit of 5-6 mm thickness.
A 14-year-old male domestic shorthair cat presented with an acute onset of aggressive behaviour, fear and hypersalivation. Neurological examination revealed bilateral mydriasis and left-sided facial twitching and hemiparesis. Magnetic resonance imaging (MRI) showed moderate bilateral symmetrical T2-hyperintensity along the entire hippocampus and bilateral asymmetric T2-hyperintensity in the pyriform lobes. Marked bilateral contrast enhancement of the hippocampus was evident on post-contrast T1-weighted images. The partial complex seizures were refractory to medical treatment and the cat was euthanased 4 days after admission. The clinical and MRI findings were consistent with feline hippocampal necrosis (FHN). On histopathology, neuronal necrosis and astrocytosis were present in the hippocampi and pyriform lobes. In addition, an oligodendroglioma was detected in the right pyriform lobe. Contrary to previous reports of FHN in which no underlying cause could be identified, we believe that in this case the seizure focus arose from a neoplastic lesion within the right pyriform lobe. This unique case report represents the so-called 'dual pathology' of temporal lobe epilepsy in humans, in which an extrahippocampal lesion within the temporal lobe results in hippocampal sclerosis.
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