Glickstein M, Kornstein M J, Pietra G G, Aronchick J M, Gefter W B, Epstein D M, Miller W
AJR Am J Roentgenol. 1986 Aug;147(2):227-37. doi: 10.2214/ajr.147.2.227.
Nonlymphomatous lymphoid disorders of the lung consist of several entities with varied histology and clinical behavior. On the basis of histologic appearance, six lesions can be identified. They include Castleman's disease, plasma-cell granuloma, pseudolymphoma, lymphocytic interstitial pneumonitis, angioimmunoblastic lymphadenopathy, and lymphomatoid granulomatosis. These conditions in 22 patients, their radiologic and histopathologic features, and their relationship to the malignant lymphomas are discussed. Although a radiographic diagnosis may be suggested, overlapping features mandate open-lung biopsy in most instances. The frequent evolution toward malignant lymphoma with lymphomatoid granulomatosis and pseudolymphoma necessitates close follow-up and sometimes aggressive therapy.
肺部非淋巴瘤性淋巴样疾病由几种具有不同组织学和临床行为的实体组成。根据组织学表现,可识别出六种病变。它们包括Castleman病、浆细胞肉芽肿、假性淋巴瘤、淋巴细胞间质性肺炎、血管免疫母细胞性淋巴结病和淋巴瘤样肉芽肿病。本文讨论了22例患者的这些病症、其放射学和组织病理学特征以及它们与恶性淋巴瘤的关系。尽管可能提示有放射学诊断,但大多数情况下,重叠的特征需要进行开胸肺活检。淋巴瘤样肉芽肿病和假性淋巴瘤常向恶性淋巴瘤演变,因此需要密切随访,有时还需要积极治疗。