Wislez M, Antoine M, Bellocq A, Carette M-F, Cadranel J
Service de Pneumologie et Réanimation Respiratoire, Hôpital Tenon, AP-HP, 4, rue de la Chine, 75970 Paris Cedex 20.
Rev Pneumol Clin. 2007 Jun;63(3):177-82. doi: 10.1016/s0761-8417(07)90122-4.
MALT lung lymphoma is a low-grade primarily B-cell lymphoma. Most cases develop in a pain free patient presenting a chronic alveolar opacity. In this review, we describe the clinical radiological and pathological features as well as the diagnostic approach to this pathological entity. Prognosis is excellent. Therapeutic options are discussed.
黏膜相关淋巴组织（MALT）型肺淋巴瘤是一种低度恶性的原发性B细胞淋巴瘤。大多数病例发生在无症状的患者身上，表现为慢性肺泡混浊。在本综述中，我们描述了这种病理实体的临床、放射学和病理学特征以及诊断方法。预后良好。文中还讨论了治疗选择。
