2014
DOI: 10.1111/vco.12127
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Splenic and hepatic ultrasound and cytology in canine lymphoma: effects of findings on stage migration and assessment of prognosis

Abstract: Stage migration is described in humans and dogs as a sequel of using more sensitive diagnostic methods. One hundred eighty-six dogs with multicentric lymphoma were enrolled with results of conventional staging as well as ultrasonographic and cytological examination of liver and spleen being available. The addition of splenic respective hepatic ultrasound and cytology findings resulted in slightly lower number of dogs classified as having liver and spleen involvement. In dogs with multicentric lymphoma, additio… Show more

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Cited by 19 publications
(21 citation statements)
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“…This led to the inclusion of dogs that had either confirmed ( n = 1) or possible ( n = 5) intra‐abdominal disease. These dogs were included in this study as they lacked peripheral lymphadenopathy, their presenting clinical signs were attributable to the presence of a large mediastinal mass, and questionable prognostic value of hepatic and splenic aspirates in lymphoma staging …”
Section: Discussionmentioning
confidence: 99%
“…This led to the inclusion of dogs that had either confirmed ( n = 1) or possible ( n = 5) intra‐abdominal disease. These dogs were included in this study as they lacked peripheral lymphadenopathy, their presenting clinical signs were attributable to the presence of a large mediastinal mass, and questionable prognostic value of hepatic and splenic aspirates in lymphoma staging …”
Section: Discussionmentioning
confidence: 99%
“…Ultrasonographic changes in homogeneity as well as echogenicity of liver and spleen were considered positive for lymphoma despite published literature 15 …”
Section: Methodsmentioning
confidence: 99%
“…A number of studies have explored methods to predict outcome in canine lymphoma including refining diagnostic staging methods using cytology and sonography to evaluate the liver and spleen [7], measurement of chemotherapy-induced neutropenia [8], assessment of the relative expression levels of BCL2 and MYC [9], the use of the modified Glasgow Prognostic Score [10]), the immunosignature at diagnosis [11], the assessment of Ki67 and its correlation with mitotic index [12] and flow cytometric characterization of S-phase fraction and ploidy in lymph node aspirates [13]. To date, no useful prognostic indicators have been established that consistently correlate with either the length or lack of remission.…”
Section: Introductionmentioning
confidence: 99%