Vilgrain V, Frija J, Yana C, Couderc L J, David M, Clauvel J P, Laval-Jeantet M
Service de Radiologie, Hôpital Saint-Louis, Paris.
J Radiol. 1989 Mar;70(3):167-73.
Three patients with lymphoid interstitial pneumonia (two HIV 1+ patients with chronic lymphadenopathic syndromes and one with a not-characterized autoimmune disease) have been studied with high-resolution computed tomography (HR-CT). This technique reveals septal lines, small reticulonodular opacities, polyhedral micronodular opacities, "ground-glass" opacities and a dense, subpleural, curved broken line in one patient. The lesions dominate in the bases of the lungs. They are not characteristic for lymphoid interstitial pneumonia. If a patient present with a chronic lymphadenopathic syndrome, the diagnosis of an opportunistic infection should not be automatically made, since the syndrome can be caused by lymphoid interstitial pneumonia.
对三名淋巴样间质性肺炎患者（两名患有慢性淋巴结病综合征的HIV 1+患者和一名患有未明确的自身免疫性疾病的患者）进行了高分辨率计算机断层扫描（HR-CT）研究。该技术显示了小叶间隔线、小的网状结节状混浊、多面形微小结节状混浊、“磨玻璃”样混浊以及一名患者中一条致密的、胸膜下的、弯曲的断线。病变主要位于肺底部。它们并非淋巴样间质性肺炎所特有。如果患者出现慢性淋巴结病综合征，不应自动诊断为机会性感染，因为该综合征可能由淋巴样间质性肺炎引起。
