Rai Manoj Ponadka, Bedi Prabhjot Singh, Marinas Edwin B, Khan Nazia Naz S
Michigan State University/Sparrow hospital B301, 788 Service Road East Lansing Michigan 48824.
UPMC East 2775 Mosside Blvd Monroeville Pennsylvania 15146.
Clin Case Rep. 2018 Feb 10;6(4):750-752. doi: 10.1002/ccr3.1388. eCollection 2018 Apr.
Angioimmunoblastic T-cell lymphoma (AITL) is a rare form of NHL and usually presents in the late stage due to the atypical laboratory findings. Immunohistochemistry of the lymph node in AITL is characterized by positive CD2, CD3, CD4, CD10, CXCL-13, PD1 often BCL-6 and CD20 positive. Meshworks of follicular dendritic cells are seen outside follicles with CD21 and CD23 stains. EBV can be often positive as well. Autologous transplantation should be offered in the first remission as poor outcome is reported with anthracycline-containing regimens.
血管免疫母细胞性T细胞淋巴瘤(AITL)是一种罕见的非霍奇金淋巴瘤(NHL)形式,由于其非典型的实验室检查结果,通常在晚期出现。AITL淋巴结的免疫组织化学特征为CD2、CD3、CD4、CD10、CXCL - 13、PD1通常呈阳性,BCL - 6和CD20也常呈阳性。用CD21和CD23染色可在滤泡外看到滤泡树突状细胞网络。EBV通常也可为阳性。由于含蒽环类药物方案的预后较差,应在首次缓解时提供自体移植。