Wall C P, Goff A M, Carrington C B, Gaensler E A
Respiration. 1979;38(6):332-44. doi: 10.1159/000194100.
Lymphomatoid granulomatosis is one of a group of pulmonary disorders characterized by necrotizing, aseptic granulomas, usually with angiitis. Multisystem dissemination is common especially to the skin and central nervous system. The diagnosis can be established only by histologic examination. Lymphomatous transformation apparently occurs in 10-20%. Treatment is generally unsatisfactory, although corticosteroids appear to be indicated initially. We present 4 patients, 3 of whom died relatively rapidly with progressive pulmonary lesions despite therapy with corticosteroids and cytotoxic agents. 1 of these patients developed a lymphoma. The fourth recovered after local excision. Pathologic diagnosis, classification, clinical and radiographic features and therapy are discussed.
淋巴瘤样肉芽肿病是一组以坏死性、无菌性肉芽肿为特征的肺部疾病之一,通常伴有血管炎。多系统播散很常见,尤其是皮肤和中枢神经系统。仅通过组织学检查才能确诊。淋巴瘤样转化显然发生在10% - 20%的病例中。尽管最初似乎需要使用皮质类固醇,但总体治疗效果并不理想。我们报告4例患者,其中3例尽管接受了皮质类固醇和细胞毒性药物治疗,但仍因进行性肺部病变而相对迅速地死亡。这些患者中有1例发展为淋巴瘤。第4例患者在局部切除后康复。本文讨论了病理诊断、分类、临床和影像学特征以及治疗方法。