Raderer Markus, Wöhrer Stefan, Streubel Berthold, Troch Marlene, Turetschek Karl, Jäger Ulrich, Skrabs Cathrin, Gaiger Alexander, Drach Johannes, Puespoek Andreas, Formanek Michael, Hoffmann Martha, Hauff Wolfgang, Chott Andreas
Department of Internal Medicine I and IV, University of Vienna, Austria.
J Clin Oncol. 2006 Jul 1;24(19):3136-41. doi: 10.1200/JCO.2006.06.0723. Epub 2006 Jun 12.
Molecular data and preliminary clinical findings have suggested mucosa-associated lymphoid tissue (MALT) lymphoma as a multifocal disease in a high percentage of patients. We report our findings with an extensive staging routine applied in patients diagnosed with MALT lymphoma at our institution.
A total of 140 consecutive patients (61 with gastric and 79 with extragastric MALT lymphoma) underwent staging according to a standardized protocol. Staging included gastroscopy with multiple biopsies, endosonography of the upper GI tract, computed tomography of thorax and abdomen, lymph node sonography, colonoscopy with multiple biopsies, otorhinolaryngologic assessment, magnetic resonance imaging of salivary and lacrimal glands, and bone marrow biopsy. All lesions suggestive of lymphoma involvement were subjected to biopsy, if accessible, and biopsies were evaluated for MALT lymphoma-specific genetic aberrations by means of reverse transcriptase polymerase chain reaction and/or fluorescent in situ hybridization.
Fifteen (25%) of 61 patients with gastric MALT lymphoma had multiorgan involvement, with dissemination beyond the GI tract in six patients. By contrast, significantly more patients with extragastric MALT lymphoma had dissemination to another MALT organ (37 of 79 patients, 46%; P = .045). Nine of these 37 patients had dissemination to the stomach. Only three (2%) of 140 patients had bone marrow involvement. Multifocality was significantly associated with t(11;18)(q21;q21) in gastric lymphomas (P = .045) and with trisomy 18 in extragastric lymphomas (P = .011).
Our findings suggest that MALT lymphoma frequently presents as a multifocal disease. Extragastric MALT lymphomas are significantly more prone to dissemination than gastric MALT lymphomas.
分子数据和初步临床研究结果表明,黏膜相关淋巴组织(MALT)淋巴瘤在高比例患者中为多灶性疾病。我们报告在本机构对诊断为MALT淋巴瘤的患者应用广泛分期程序后的研究结果。
总共140例连续患者(61例胃MALT淋巴瘤患者和79例胃外MALT淋巴瘤患者)按照标准化方案进行分期。分期包括多次活检的胃镜检查、上消化道内镜超声检查、胸部和腹部计算机断层扫描、淋巴结超声检查、多次活检的结肠镜检查、耳鼻喉科评估、唾液腺和泪腺磁共振成像以及骨髓活检。所有提示淋巴瘤受累的病变,若可及则进行活检,并通过逆转录聚合酶链反应和/或荧光原位杂交对活检组织进行MALT淋巴瘤特异性基因畸变评估。
61例胃MALT淋巴瘤患者中有15例(25%)有多器官受累,6例患者的病变播散至胃肠道以外。相比之下,胃外MALT淋巴瘤患者中有更多患者病变播散至另一个MALT器官(79例患者中有37例,46%;P = 0.045)。这37例患者中有9例病变播散至胃部。140例患者中仅有3例(2%)有骨髓受累。多灶性在胃淋巴瘤中与t(11;18)(q21;q21)显著相关(P = 0.045),在胃外淋巴瘤中与18号染色体三体显著相关(P =