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Clonality assessment of lymphoproliferative lesions using the polymerase chain reaction: An analysis of two methods.
Indian J Pathol Microbiol ; 2011 Apr-Jun 54(2): 330-334
Article in English | IMSEAR | ID: sea-141994
ABSTRACT

Background:

Lymphoid malignancies are a heterogeneous group of disorders which may be difficult to differentiate from reactive proliferations even after immunohistochemistry. Polymerase chain reaction (PCR) is believed to be a good adjunct tool for diagnosis. Materials and

Methods:

We examined 24 cases of neoplastic and non-neoplastic lymphoproliferative lesions in this study and evaluated the PCR as an additional tool in the confirmation of the diagnosis. Two different PCR methodologies were evaluated.

Results:

In the evaluation of the T-cell PCR, it was seen that the correlation using both the commercial kits and the custom-synthesized primers was highly significant at a P value of <0.05. In the evaluation of the B-cell PCR, it was seen that the correlation using both the commercial kits and the custom-synthesized primers was not significant using either method (P > 0.05).

Conclusions:

Both the methods showed an excellent concordance for T-cell γ gene rearrangements, However, the same was not seen in the B-cell receptor rearrangements. This may be because of the small sample size or the inability of consensus V primers to recognize complementary DNA sequences in all of the V segments.
Subject(s)

Full text: Available Index: IMSEAR (South-East Asia) Main subject: Reagent Kits, Diagnostic / Humans / T-Lymphocytes / Polymerase Chain Reaction / Clone Cells / DNA Primers / Pathology, Molecular / Lymphoproliferative Disorders Type of study: Diagnostic study Language: English Journal: Indian J Pathol Microbiol Year: 2011 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Reagent Kits, Diagnostic / Humans / T-Lymphocytes / Polymerase Chain Reaction / Clone Cells / DNA Primers / Pathology, Molecular / Lymphoproliferative Disorders Type of study: Diagnostic study Language: English Journal: Indian J Pathol Microbiol Year: 2011 Type: Article