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联合组织学与分子生物学用于早期胃黏膜相关淋巴组织淋巴瘤的诊断

Combined histology and molecular biology for diagnosis of early stage gastric MALT lymphoma.

作者信息

Yi Zhi Hui, Ouyang Qin, Li Gan Di, Chen Dai Yun

机构信息

Department of Gastroenterology, West China Hospital, Sichuan Universty, Chengdu, Sichuan Province, China.

出版信息

Chin J Dig Dis. 2006;7(1):12-8. doi: 10.1111/j.1443-9573.2006.00238.x.

Abstract

OBJECTIVE

To establish a sequential diagnostic procedure of gastric mucosa-associated lymphoid tissue (MALT) lymphoma and provide evidence for selected optimal cases to be treated in the early stage.

METHODS

Thirty-one cases of gastric lymphoid hyperplasia (GLH) were selected and multiple investigations including histology, protein level, DNA and chromosome levels, combined with clinical follow-up were performed. Histological grade was according to Isaacson's criteria of GLH; CD20, UCHL-1 (CD45RO), anti-kappa (kappa), anti-lambda (lambda) and Ki-67 were used for immunohistochemical staining; semi-nested polymerase chain reaction (PCR) was used to detect IgH gene rearrangement and reverse-transcription PCR (RT-PCR) was used to detect API2-MALT1 fusion of the chromosome translocation t(11;18)(q21;q21). Twenty-nine cases underwent eradication therapy for Helicobacter pylori. Changes in histological grade, endoscopic appearance, expression of Ki-67 and IgH gene rearrangement were compared after eradication treatment.

RESULTS

Of the 31 cases of GLH with predominant chronic gastritis and gastric ulcer most were histological grade 2 and 3. Only one case had lambda light chain restriction and 10 cases had monoclonal IgH gene rearrangement. Expression of Ki-67 and monoclonal IgH gene rearrangement were significantly increased with increased lymphoid hyperplasia (P < 0.05). Two cases had API2-MALT1 fusion. Helicobacter pylori was eradicated in 25 cases and another course of treatment had to be given in 4 cases. All cases were followed up for 1.5-37 months. Of the 27 successful eradication cases, 18 showed complete regression both histologically and endoscopically, 4 had partial regression and 7 were unchanged.

CONCLUSIONS

A sequential diagnostic procedure based on histology, expression of Ki-67 combined with clonality of IgH rearrangement and API2-MALT1 fusion helps to diagnosis of early stage gastric MALT lymphoma and choose the best treatment strategy.

摘要

目的

建立胃黏膜相关淋巴组织(MALT)淋巴瘤的序贯诊断程序,并为选择早期治疗的最佳病例提供依据。

方法

选取31例胃淋巴组织增生(GLH)病例,进行包括组织学、蛋白质水平、DNA和染色体水平在内的多项检查,并结合临床随访。组织学分级依据Isaacson的GLH标准;采用CD20、UCHL-1(CD45RO)、抗κ(kappa)、抗λ(lambda)和Ki-67进行免疫组织化学染色;采用半巢式聚合酶链反应(PCR)检测IgH基因重排,采用逆转录PCR(RT-PCR)检测染色体易位t(11;18)(q21;q21)的API2-MALT1融合。29例患者接受了幽门螺杆菌根除治疗。比较根除治疗后组织学分级、内镜表现、Ki-67表达及IgH基因重排的变化。

结果

31例以慢性胃炎和胃溃疡为主的GLH病例中,多数为组织学2级和3级。仅1例有λ轻链限制,10例有单克隆IgH基因重排。Ki-67表达和单克隆IgH基因重排随淋巴组织增生增加而显著升高(P<0.05)。2例有API2-MALT1融合。25例幽门螺杆菌被根除,4例需再次治疗。所有病例随访1.5~37个月。27例成功根除病例中,18例组织学和内镜均完全缓解,4例部分缓解,7例无变化。

结论

基于组织学、Ki-67表达结合IgH重排的克隆性及API2-MALT1融合的序贯诊断程序有助于早期胃MALT淋巴瘤的诊断及选择最佳治疗策略。

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