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Cross Lineage Rearrangement in Feline Enteropathy-Associated T-cell Lymphoma.

C Andrews1, M Operacz2, R Maes2

  • 1Diagnostic Center for Population and Animal Health, Michigan State University, Lansing, MI, USA Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, USA caroline.andrews@nih.gov.

Veterinary Pathology
|July 29, 2015
PubMed
Summary
This summary is machine-generated.

Cross lineage rearrangement occurs in 8.7% of feline enteropathy-associated T-cell lymphoma (EATL) type II. Polymerase chain reaction (PCR) for antigen receptor rearrangements (PARR) aids in diagnosing EATL by detecting immunoglobulin heavy chain (IGH) gene rearrangements.

Keywords:
PARRTCRGfelinegastrointestinal neoplasmslymphomareceptor rearrangement

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Area of Science:

  • Veterinary Pathology
  • Canine and Feline Oncology
  • Molecular Diagnostics

Background:

  • Feline enteropathy-associated T-cell lymphoma (EATL) type II presents diagnostic challenges, often mimicking inflammatory conditions due to small T-cell infiltration.
  • Polymerase chain reaction (PCR) for antigen receptor rearrangements (PARR) is crucial for differentiating EATL from inflammation by assessing T-cell receptor gamma (TCRG) and immunoglobulin heavy chain (IGH) gene rearrangements.

Purpose of the Study:

  • To determine the incidence of cross lineage rearrangement in feline EATL type II.
  • To evaluate the utility of PARR testing in diagnosing feline EATL type II, particularly when TCRG gene rearrangements are polyclonal.

Main Methods:

  • A diagnostic algorithm integrating histology, immunohistochemistry, and PARR testing was employed.
  • Analysis of 92 feline cases diagnosed as EATL type II between January 2013 and June 2014.
  • Assessment of both TCRG and IGH gene rearrangements using PARR.

Main Results:

  • Cross lineage rearrangement was identified in 8.7% (8 of 92) of feline EATL type II cases.
  • PARR testing for the IGH gene proved valuable in diagnosing cases with suspected EATL type II and polyclonal TCRG rearrangement.
  • This highlights the complexity of lymphocyte clonality in feline EATL.

Conclusions:

  • Cross lineage rearrangement is an important consideration in the diagnosis of feline EATL type II.
  • Integrating PARR, especially IGH gene analysis, with traditional methods improves diagnostic accuracy.
  • Accurate differentiation of EATL from inflammation is critical for appropriate feline patient management.