Yoon Sam S, Coit Daniel G, Portlock Carol S, Karpeh Martin S
Department of Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
Ann Surg. 2004 Jul;240(1):28-37. doi: 10.1097/01.sla.0000129356.81281.0c.
This article reviews the pathogenesis, diagnosis, and treatment of patients with primary gastric lymphoma, with special attention to the changing role of surgery.
Primary gastric lymphomas are non-Hodgkin lymphomas that originate in the stomach and are divided into low-grade (or indolent) and high-grade (or aggressive) types. Low-grade lesions nearly always arise from mucosa-associated lymphoid tissue (MALT) secondary to chronic Helicobacter pylori (H. pylori) infection and disseminate slowly. High-grade lesions may arise from a low grade-MALT component or arise de novo and can spread to lymph nodes, adjacent organs and tissues, or distant sites.
A review of the relevant English-language articles was performed on the basis of a MEDLINE search from January 1984 to August 2003.
About 40% of gastric lymphomas are low-grade, and nearly all these low-grade lesions are classified as MALT lymphomas. For low-grade MALT lymphomas confined to the gastric wall and without certain negative prognostic factors, H. pylori eradication is highly successful in causing lymphoma regression. More advanced low-grade lymphomas or those that do not regress with antibiotic therapy can be treated with combinations of H. pylori eradication, radiation therapy, and chemotherapy. Nearly 60% of gastric lymphomas are high-grade lesions with or without a low-grade MALT component. These lymphomas can be treated with chemotherapy and radiation therapy according to the extent of disease. Surgery for gastric lymphoma is now often reserved for patients with localized, residual disease after nonsurgical therapy or for rare patients with complications.
The treatment of gastric lymphoma continues to evolve, and surgical resection is now uncommonly a part of the initial management strategy.
本文回顾原发性胃淋巴瘤患者的发病机制、诊断及治疗,特别关注手术作用的变化。
原发性胃淋巴瘤是非霍奇金淋巴瘤,起源于胃,分为低度(或惰性)和高度(或侵袭性)类型。低度病变几乎总是继发于慢性幽门螺杆菌(H. pylori)感染的黏膜相关淋巴组织(MALT),且进展缓慢。高度病变可能源于低度MALT成分或原发产生,可扩散至淋巴结、邻近器官和组织或远处部位。
基于1984年1月至2003年8月的MEDLINE检索,对相关英文文章进行综述。
约40%的胃淋巴瘤为低度,几乎所有这些低度病变都归类为MALT淋巴瘤。对于局限于胃壁且无特定不良预后因素的低度MALT淋巴瘤,根除幽门螺杆菌在使淋巴瘤消退方面非常成功。更晚期的低度淋巴瘤或对抗生素治疗无反应的淋巴瘤,可采用根除幽门螺杆菌、放疗和化疗联合治疗。近60%的胃淋巴瘤为高度病变,有或无低度MALT成分。这些淋巴瘤可根据疾病范围采用化疗和放疗。胃淋巴瘤手术现在通常适用于非手术治疗后局部残留疾病的患者或罕见的有并发症的患者。
胃淋巴瘤的治疗不断发展,手术切除现在很少成为初始治疗策略的一部分。