Andrews C, Operacz M, Maes R, Kiupel M
Diagnostic 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
Diagnostic Center for Population and Animal Health, Michigan State University, Lansing, MI, USA.
Vet Pathol. 2016 May;53(3):559-62. doi: 10.1177/0300985815595518. Epub 2015 Jul 27.
Feline enteropathy-associated T-cell lymphoma (EATL) type II is characterized by infiltration of the small intestinal mucosa with small T-cells with variable epitheliotropism and is often difficult to differentiate from inflammation. Polymerase chain reaction (PCR) to assess antigen receptor rearrangements (PARR) amplifies the T- (T-cell receptor gamma, TCRG) or B-cell (immunoglobulin heavy chain, IGH) antigen receptor genes and is used to differentiate EATL from inflammation. However, PARR does not determine lymphocyte phenotype, and clonal rearrangement of either or both the TCRG or IGH genes may be detected in neoplastic T-cells. The purpose of this study was to determine the incidence of cross lineage rearrangement in feline EATL type II. Using a diagnostic algorithm combining histology, immunohistochemistry, and PARR testing, 8 of 92 cases diagnosed as EATL type II at Michigan State University between January 2013 and June 2014 showed cross lineage rearrangement (8.7%). PARR for the IGH gene facilitates the diagnosis of cases histologically highly suggestive of EATL type II in which polyclonal rearrangement of the TCRG gene is detected.
II型猫肠道病相关T细胞淋巴瘤(EATL)的特征是小肠黏膜被具有不同上皮嗜性的小T细胞浸润,且常难以与炎症区分。评估抗原受体重排(PARR)的聚合酶链反应(PCR)可扩增T细胞(T细胞受体γ,TCRG)或B细胞(免疫球蛋白重链,IGH)抗原受体基因,用于区分EATL与炎症。然而,PARR并不能确定淋巴细胞表型,并且在肿瘤性T细胞中可能检测到TCRG或IGH基因之一或两者的克隆重排。本研究的目的是确定II型猫EATL中跨谱系重排的发生率。使用结合组织学、免疫组织化学和PARR检测的诊断算法,在2013年1月至2014年6月期间,密歇根州立大学诊断为II型EATL的92例病例中有8例显示跨谱系重排(8.7%)。IGH基因的PARR有助于诊断组织学上高度提示II型EATL且检测到TCRG基因多克隆重排的病例。