2012
DOI: 10.1177/1098612x12439266
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Feline alimentary lymphoma

Abstract: The evidence supporting this review is derived from grade II, III and IV prospective studies, retrospective case series, reviews, extrapolation from other species, pathophysiological justification and the combined clinical experience of those working in the field.

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Cited by 47 publications
(46 citation statements)
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“…It is a minimally invasive and rapid technique allowing macroscopic lesions to be described and multiple intestinal biopsy samples to be collected, albeit exclusively from mucosa or submucosa [ 15 , 20 , 72 , 105 ]. Mucosal lesions that cannot be characterised by ultrasonographic examination may be identified by endoscopy [ 75 , 106 , 107 ]. Macroscopic differentiation between inflammatory lesions (congestion, oedema, mucosal fibrosis) and LGAL lesions is not possible by endoscopic examination [ 20 , 107 ].…”
Section: Diagnosismentioning
confidence: 99%
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“…It is a minimally invasive and rapid technique allowing macroscopic lesions to be described and multiple intestinal biopsy samples to be collected, albeit exclusively from mucosa or submucosa [ 15 , 20 , 72 , 105 ]. Mucosal lesions that cannot be characterised by ultrasonographic examination may be identified by endoscopy [ 75 , 106 , 107 ]. Macroscopic differentiation between inflammatory lesions (congestion, oedema, mucosal fibrosis) and LGAL lesions is not possible by endoscopic examination [ 20 , 107 ].…”
Section: Diagnosismentioning
confidence: 99%
“…Mucosal lesions that cannot be characterised by ultrasonographic examination may be identified by endoscopy [ 75 , 106 , 107 ]. Macroscopic differentiation between inflammatory lesions (congestion, oedema, mucosal fibrosis) and LGAL lesions is not possible by endoscopic examination [ 20 , 107 ]. In addition, the jejunum and the proximal part of the ileum, which are the most frequent locations of LGAL, are often not accessible by endoscopy [ 105 ].…”
Section: Diagnosismentioning
confidence: 99%
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