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黏膜相关淋巴组织淋巴瘤

MALT Lymphomas.

作者信息

Malek Sami N, Hatfield Amy J, Flinn Ian W

机构信息

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1650 Orleans Street, CRB Room 388, Baltimore, MD 21231, USA.

出版信息

Curr Treat Options Oncol. 2003 Aug;4(4):269-79. doi: 10.1007/s11864-003-0002-2.

Abstract

Mucosa-associated lymphoid tissue (MALT) lymphomas occur in a variety of organs, including the orbit, conjunctiva, salivary glands, skin, thyroid gland, lungs, stomach, and intestine. These tumors are often localized and of indolent clinical behavior. Diagnosis is made by pathologic evaluation of a tissue biopsy. Careful staging is mandatory and tailored to the initial presentation. Staging includes a history and physical, chemistries, computed tomography scan, and bone marrow biopsy. This information is supplemented with an ear, nose, and throat consultation, esophagogastro-duodenoscopy, colonoscopy, endoscopic ultrasound of the stomach, and cytogenetic/immunohistochemical analysis of the tumors. Treatment is tailored to organ involvement and stage at presentation. Eradication of Helicobacter pylori using a triple anti-H. pylori regimen approved by the US Food and Drug Administration is standard therapy for all H. pylori-positive gastric MALT lymphomas. Endoscopic ultrasound- and computed tomography-staged gastric MALT stage IE tumors will achieve a complete response with this approach in approximately 60% to 90% of patients (the more superficial the tumor, the better the response). Patients with tumors that are T4 node-positive Musshoff stage IIE1 and IIE2 or tumors with adverse cytogenetics should receive radiotherapy or surgery with or without radiotherapy. Tumors with a significant high-grade component or large cell tumors with a minor low-grade MALT component should receive CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)-based chemotherapy. Localized MALT lymphomas of the orbit, conjunctiva, salivary glands, and thyroid gland are treated successfully with radiotherapy. Surgery as first-line therapy for gastric MALT lymphomas was replaced by attempts at organ preservation. In the past, margin-free surgical excision or tumor debulking followed by radiation therapy and chemotherapy has been highly effective for gastric MALT lymphomas. Therefore, surgical excision of large cell or bulky tumors of the stomach, thyroid, lung, and salivary gland, followed by adjuvant radiotherapy or chemotherapy, may still be an important consideration in selected patients. Surgery still has a role for patients with relapsed or refractory low-grade disease and life-threatening hemorrhage. Disseminated MALT lymphomas are incurable and are treated primarily with chemotherapy according to symptoms.

摘要

黏膜相关淋巴组织(MALT)淋巴瘤可发生于多种器官,包括眼眶、结膜、唾液腺、皮肤、甲状腺、肺、胃和肠道。这些肿瘤通常局限,临床行为惰性。通过组织活检的病理评估进行诊断。必须进行仔细分期,并根据初始表现进行调整。分期包括病史和体格检查、血液检查、计算机断层扫描以及骨髓活检。这些信息还需补充耳鼻喉科会诊、食管胃十二指肠镜检查、结肠镜检查、胃内镜超声检查以及肿瘤的细胞遗传学/免疫组织化学分析。治疗方案根据器官受累情况和就诊时的分期进行调整。使用美国食品药品监督管理局批准的三联抗幽门螺杆菌方案根除幽门螺杆菌是所有幽门螺杆菌阳性胃MALT淋巴瘤的标准治疗方法。经内镜超声和计算机断层扫描分期的胃MALT ⅠE期肿瘤采用这种方法,约60%至90%的患者可实现完全缓解(肿瘤越表浅,缓解效果越好)。肿瘤为T4淋巴结阳性的Musshoff ⅡE1和ⅡE2期患者或细胞遗传学不良的肿瘤患者应接受放疗或手术联合或不联合放疗。具有显著高级别成分的肿瘤或具有少量低级别MALT成分的大细胞肿瘤应接受基于CHOP(环磷酰胺、阿霉素、长春新碱和泼尼松)的化疗。眼眶、结膜、唾液腺和甲状腺的局限性MALT淋巴瘤通过放疗可成功治疗。胃MALT淋巴瘤的一线治疗已从手术转变为尝试器官保留。过去,无边缘手术切除或肿瘤减积后联合放疗和化疗对胃MALT淋巴瘤非常有效。因此,对于胃、甲状腺、肺和唾液腺的大细胞或体积较大的肿瘤,手术切除后联合辅助放疗或化疗,在特定患者中可能仍是重要的考虑方案。手术对于复发或难治性低级别疾病以及危及生命的出血患者仍有作用。播散性MALT淋巴瘤无法治愈,主要根据症状进行化疗。

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