2004
DOI: 10.1111/j.1939-165x.2004.tb00364.x
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Detection of neoplastic lymphocytes in peripheral blood of dogs with lymphoma by polymerase chain reaction for antigen receptor gene rearrangement

Abstract: PCR is more sensitive than microscopy for the detection of clonal lymphocytes in peripheral blood. The results of this study also suggest that neoplastic lymphocytes circulate in peripheral blood at a higher frequency than previously reported. PCR may be useful for detecting or phenotyping lymphoma, monitoring response to therapy, identifying recurrence, and screening breeds at risk.

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Cited by 41 publications
(32 citation statements)
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“…4 More recently, a similar assay was developed based on the canine genome database by targeting the T-cell receptor gamma chain (TCRc) gene 15 and the immunoglobulin heavy chain (IgH) gene. 9 Although the diagnostic value of PCR analysis has been demonstrated in several types of lymphoproliferative disorders, 7,[11][12][13][14] only limited studies have been done to identify neoplastic proliferation of lymphocytes in dogs with small-cell lymphocytosis. In the present study, immunophenotypical evaluation was performed on the blood of dogs with small lymphocytosis.…”
Section: Introductionmentioning
confidence: 99%
“…4 More recently, a similar assay was developed based on the canine genome database by targeting the T-cell receptor gamma chain (TCRc) gene 15 and the immunoglobulin heavy chain (IgH) gene. 9 Although the diagnostic value of PCR analysis has been demonstrated in several types of lymphoproliferative disorders, 7,[11][12][13][14] only limited studies have been done to identify neoplastic proliferation of lymphocytes in dogs with small-cell lymphocytosis. In the present study, immunophenotypical evaluation was performed on the blood of dogs with small lymphocytosis.…”
Section: Introductionmentioning
confidence: 99%
“…So PARR is an objective and highly sensitive method to detect clonal populations of B or T lymphocytes (Burnett et al, 2003). The sensitivity of PARR for detecting lymphoma cells may provide a noninvasive method for detecting lymphoma in its early stages, determining phenotype, monitoring therapy, screening breeds at risk for lymphoma, and possibly for assessing prognosis (Keller et al, 2004). Also, this method can be applied for the diagnosis of lymphoma from limited biopsy samples, formalin-fixed/paraffin-embedded tissues (Wan et al, 1990;Tai and Peh, 2003), or even sections already mounted on slides and stained (Fend et al, 1999;Yu et al, 2009).…”
Section: Discussionmentioning
confidence: 99%
“…The stage of canine lymphoma is currently diagnosed primarily by morphological assessment of lymphoid tissue based on subjective lightmicroscopic assessments (Keller et al, 2004;Tamura et al, 2006). Although this definition of stage V lymphoma appears easy, microscopic criteria are subjective and varied to detect neoplastic cells in lymph node and peripheral blood.…”
Section: Discussionmentioning
confidence: 99%
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“…In PARR, clonal expansion of tumor lymphocytes that contain a rearranged immunoglobulin heavy chain (IgH) gene or a T cell receptor gamma (TCR) gene can be detected in B-cell and T-cell lymphoid neoplasias, respectively. PARR is an objective and highly sensitive method, and its usefulness in diagnosis of canine lymphoid neoplasia has recently been proven [3,8,10,17]. In the present study, we evaluated the usefulness of PARR using endoscopic biopsy specimens in diagnosis of alimentary lymphoma.…”
mentioning
confidence: 99%