Hashimoto Y, Nakamura N, Kuze T, Ono N, Abe M
1st Department of Pathology, School of Medicine, Fukushima Medical University, Japan.
Hum Pathol. 1999 May;30(5):581-7. doi: 10.1016/s0046-8177(99)90205-8.
Multiple lymphomatous polyposis (MLP) is characterized by multiple polyps involving long segments of the gastrointestinal (GI) tract. MLP is thought to represent mantle cell lymphoma (MCL) of the GI tract; however, some cases of follicular lymphoma (FL) of the GI tract are found with a multiple polypoid appearance. In the present study, to clarify the cellular origin of MLP, clonal immunoglobulin heavy chain (IgH) gene rearrangement of four cases with MLP was amplified by polymerase chain reaction (PCR) and analyzed for the presence of somatic mutation. The IgH variable (VH) region sequences of three cases (CD5+ CD10- cyclin D1+) showed a little somatic mutation compared with the closest published germline. The other case (CD10+ CD5- cyclin D1-) was highly mutated and showed intraclonal heterogeneity (ongoing somatic hypermutation). These data indicate that three of the cases with MLP are derived from pregerminal center B cells (mantle zone B cells) and one case with MLP from germinal center B cells. Our study suggests that MLP is a heterogenous group that includes MCL and FL.
多发性淋巴瘤性息肉病(MLP)的特征是胃肠道(GI)长段出现多个息肉。MLP被认为代表胃肠道的套细胞淋巴瘤(MCL);然而,胃肠道的一些滤泡性淋巴瘤(FL)病例也呈现出多发性息肉样外观。在本研究中,为了阐明MLP的细胞起源,通过聚合酶链反应(PCR)扩增了4例MLP患者的克隆性免疫球蛋白重链(IgH)基因重排,并分析了体细胞突变的存在情况。3例(CD5 + CD10 - 细胞周期蛋白D1 +)的IgH可变(VH)区序列与最接近的已发表种系相比,体细胞突变较少。另一例(CD10 + CD5 - 细胞周期蛋白D1 -)高度突变,并表现出克隆内异质性(正在进行的体细胞超突变)。这些数据表明,3例MLP病例源自生发中心前B细胞(套区B细胞),1例MLP病例源自生发中心B细胞。我们的研究表明,MLP是一个异质性群体,包括MCL和FL。