Sterry W, Staib G
Abteilung Dermatologie, Universität Ulm.
Hautarzt. 1995 Jan;46(1):4-9. doi: 10.1007/s001050050199.
The diagnosis of cutaneous malignant lymphoma is based on clinical, histo-morphological and immunochemical findings and, now a days, on molecular biology analyses of the genotype in the lymphocytic infiltrate. By using the polymerase chain reaction (PCR) with specific primers for the Ig heavy chain gene and the T-cell receptor gamma chain gene, the detection of monoclonal cell populations in the skin infiltrate is possible. Since this method produces results within 3 days, since paraffin-embedded skin and lymph node biopsies and heparinized peripheral blood can be used and since no radioactivity is necessary, this technique has important advantages over traditional techniques such as Southern blot analyses. In addition, specific PCR analyses may allow a patient-specific monitoring during therapy and also may detect early relapses of the lymphoproliferative malignant disease.
皮肤恶性淋巴瘤的诊断基于临床、组织形态学和免疫化学检查结果,如今还基于对淋巴细胞浸润物基因型的分子生物学分析。通过使用针对免疫球蛋白重链基因和T细胞受体γ链基因的特异性引物进行聚合酶链反应(PCR),可以检测皮肤浸润物中的单克隆细胞群。由于该方法在3天内即可得出结果,由于石蜡包埋的皮肤和淋巴结活检组织以及肝素化外周血均可使用,且无需放射性,因此该技术相对于传统技术(如Southern印迹分析)具有重要优势。此外,特异性PCR分析可在治疗期间对患者进行个体化监测,还可检测淋巴增殖性恶性疾病的早期复发。