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原发性肺淋巴瘤。70例非免疫功能低下患者的临床研究。

Primary pulmonary lymphomas. A clinical study of 70 cases in nonimmunocompromised patients.

作者信息

Cordier J F, Chailleux E, Lauque D, Reynaud-Gaubert M, Dietemann-Molard A, Dalphin J C, Blanc-Jouvan F, Loire R

机构信息

Hôpital Cardiovasculaire et Pneumologique, Claude Bernard University, Lyon, France.

出版信息

Chest. 1993 Jan;103(1):201-8. doi: 10.1378/chest.103.1.201.

Abstract

We studied 70 patients with biopsy-proven pulmonary non-Hodgkin's lymphomas without extrathoracic involvement or mediastinal adenopathy to determine the clinical, imaging, and endoscopic features of this condition in a homogeneous series. In low-grade (LG) lymphomas, symptoms were cough, dyspnea, chest pain, hemoptysis. Imaging features consisted of localized alveolar opacities, infiltrative diffuse opacities, atelectasis, and pleural effusions. Inflammatory changes of the mucosa were present in some patients, leading to bronchial stenosis in 7; biopsies showed lymphomatous infiltration in 12. Prognosis of LG lymphomas was excellent, with 93.6 percent survival at five years. High-grade lymphomas differed from LG lymphomas principally by a more aggressive course and a worse survival. Inflammatory changes occurred in seven of nine cases leading to stenosis in two, and biopsies showed lymphomatous involvement in five. The profile of primary pulmonary lymphomas in this study could help clinicians consider this condition and prompt them to evaluate new diagnostic tools.

摘要

我们研究了70例经活检证实的无胸外受累或纵隔淋巴结肿大的肺非霍奇金淋巴瘤患者,以确定这一同质系列病例的临床、影像学和内镜特征。在低度(LG)淋巴瘤中,症状包括咳嗽、呼吸困难、胸痛、咯血。影像学特征包括局限性肺泡实变、浸润性弥漫性实变、肺不张和胸腔积液。部分患者存在黏膜炎症改变,7例导致支气管狭窄;12例活检显示淋巴瘤浸润。LG淋巴瘤的预后极佳,五年生存率为93.6%。高度淋巴瘤与LG淋巴瘤的主要区别在于病程更具侵袭性,生存率更低。9例中有7例出现炎症改变,2例导致狭窄,5例活检显示有淋巴瘤累及。本研究中原发性肺淋巴瘤的特征有助于临床医生考虑这一疾病,并促使他们评估新的诊断工具。

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