Bhagavathi Sharathkumar, Blenc A M, Amin M, Nikitin V D, Patel M C, Warren S, Malhotra R K
Department of Pathology and Laboratory Medicine, Division of Hematopathology, Indiana University, 350 W 11th Street, Indianapolis, IN 46022, USA.
Am J Dermatopathol. 2010 Jul;32(5):439-41. doi: 10.1097/DAD.0b013e3181c1195b.
Primary cutaneous lymphomas are defined as lymphomas, which are present in the skin without evidence of extracutaneous disease at the time of diagnosis. Primary cutaneous large B-cell lymphoma (PCLBCL) is a subtype of primary cutaneous B-cell lymphoma with a female predominance, occurring in elderly patients and known to have unfavorable prognosis. We evaluated 10 cases of PCLBCL in immunocompetent patients between 2005 and 2008. A panel of immunoperoxidase stains; CD3, CD10, CD20, BCL2, BCL6, and MUM1 were performed on all cases. Nuclear factor kappa B (NF-kappaB) pathway activation was evaluated using an immunostain for P65. The presence of Epstein-Barr virus (EBV) was assessed using Epstein-Barr virus encoded RNA (EBER) in situ hybridization probe. All cases were CD20 positive and CD3 negative. CD10, BCL6, BCL2, and MUM1 were positive in 4/10 (40%), 6/10 (60%), 7/10 (70%), and 7/10 (70%) cases, respectively. NF-kappaB activation was detected in 7/10 (70%) cases. One (10%) case was positive for EBV by in situ hybridization. Interestingly, the EBV positive case was also positive for MUM1 and negative for CD10, indicating an activated immunophenotype. In conclusion, majority of PCLBCL shows activation of NF-kappaB pathway with a low incidence of EBV.
原发性皮肤淋巴瘤被定义为在诊断时仅存在于皮肤而无皮肤外疾病证据的淋巴瘤。原发性皮肤大B细胞淋巴瘤(PCLBCL)是原发性皮肤B细胞淋巴瘤的一种亚型,女性多见,发生于老年患者,预后不良。我们评估了2005年至2008年间10例免疫功能正常患者的PCLBCL。对所有病例进行了一组免疫过氧化物酶染色;CD3、CD10、CD20、BCL2、BCL6和MUM1。使用P65免疫染色评估核因子κB(NF-κB)途径的激活。使用爱泼斯坦-巴尔病毒编码RNA(EBER)原位杂交探针评估爱泼斯坦-巴尔病毒(EBV)的存在。所有病例CD20阳性,CD3阴性。CD10、BCL6、BCL2和MUM1分别在4/10(40%)、6/10(60%)、7/10(70%)和7/10(70%)的病例中呈阳性。在7/10(70%)的病例中检测到NF-κB激活。1例(10%)原位杂交检测EBV阳性。有趣的是,EBV阳性病例MUM1也呈阳性,CD10呈阴性,表明免疫表型激活。总之,大多数PCLBCL显示NF-κB途径激活,EBV发生率低。