Department of Hematopathology, The University of Texas M. D. Anderson Cancer Center, Houston, 77030, USA.
Am J Clin Pathol. 2010 Jul;134(1):112-8. doi: 10.1309/AJCP0HT6ZGSZKNFT.
Patients with mucosa-associated lymphoid tissue (MALT) lymphoma often have multiple sites of disease at initial diagnosis or during the clinical course. The neoplasms at multiple sites are often presumed to be identical, indicating dissemination or relapse. However, evidence to support this presumption is usually not available. We compared IGH VDJ sequences in 4 patients with 2 sequential sites of MALT lymphoma. The specimen pairs were stomach and nasopharynx, stomach and lung, ocular adnexa and nasopharynx, and ocular adnexa and parotid gland. The median interval between biopsies was 4 months (range, 1-32 months). Monoclonal IGH gene rearrangement was detected in all cases. In 3 patients, the VDJ sequences were distinct; in 1 patient the 2 biopsy specimens shared the same clone. MALT lymphomas involving multiple sites in a patient are usually not clonally related but arise independently, likely due to chronic antigenic stimulation, inducing oligoclonal B-cell proliferations and eventually a dominant B-cell clone.
患者黏膜相关淋巴组织(MALT)淋巴瘤往往在初始诊断或临床病程中有多个部位的疾病。多个部位的肿瘤通常被认为是相同的,表明其传播或复发。然而,通常没有支持这一假设的证据。我们比较了 4 例 MALT 淋巴瘤 2 个连续部位的IGH VDJ 序列。标本对为胃和鼻咽部、胃和肺部、眼附属器和鼻咽部以及眼附属器和腮腺。活检之间的中位间隔为 4 个月(范围为 1-32 个月)。所有病例均检测到单克隆IGH 基因重排。在 3 例患者中,VDJ 序列不同;在 1 例患者中,2 个活检标本共享相同的克隆。患者多个部位的 MALT 淋巴瘤通常不是克隆相关的,而是独立发生的,可能是由于慢性抗原刺激,诱导寡克隆 B 细胞增殖,最终导致一个优势 B 细胞克隆。