Movilia A, De Servi B, Assi A
Unità Operativa di Anatomia e Istologia Patologica, Azienda Ospedaliera, Ospedale Civile di Legnano.
Pathologica. 2000 Jun;92(3):172-6.
The application of PCR to detect monoclonality at the immunoglobulin heavy chain gene locus in FNA cytologic specimens was evaluated.
Immunoglobulin heavy chain gene rearrangement analysis was performed by a nested PCR for the VDJ region on 27 lymph nodes FNA paraffin embedded by cell blocking technique specimens (1 suspicious of NOS lymphoma, 1 Hodgkin's disease, 6 B cell non Hodgkin's lymphomas, 10 reactive hyperplasias).
A monoclonal band was seen in 13 of 17 suspicious or positive malignant cases. The other 4 specimens gave a policlonal pattern. Specimens from reactive lymph nodes produced policlonal bands in 8 cases, no product in 1 case and 1 specimen gave a monoclonal band. When needed, the results of PCR examinations were compared with the subsequent histologic evaluation of the same lymph-node.
From our experience we can see that clonal analysis by PCR based IgH gene rearrangement analysis can be applied to FNA material and can be useful in diagnosis.
评估了聚合酶链反应(PCR)在细针穿刺(FNA)细胞学标本的免疫球蛋白重链基因位点检测单克隆性中的应用。
采用巢式PCR对27例经细胞块技术包埋的FNA石蜡包埋淋巴结标本(1例疑似未另行分类淋巴瘤、1例霍奇金病、6例B细胞非霍奇金淋巴瘤、10例反应性增生)的VDJ区域进行免疫球蛋白重链基因重排分析。
17例可疑或阳性恶性病例中有13例出现单克隆条带。其他4份标本呈现多克隆模式。反应性淋巴结标本8例产生多克隆条带,1例无产物,1份标本出现单克隆条带。必要时,将PCR检测结果与同一淋巴结随后的组织学评估结果进行比较。
根据我们的经验,基于PCR的免疫球蛋白重链基因重排分析进行的克隆分析可应用于FNA材料,对诊断有帮助。