Zhang Lian-bin, Sun Yu-e, Yu Chang-hai, Liu Ying
Department of Thoracic Surgery, General Hospital of People's Liberation Army, Beijing 100853, China.
Zhonghua Wai Ke Za Zhi. 2006 Jan 15;44(2):97-9.
To study the clinical characteristics, the principles of diagnosis and surgical treatment for primary pulmonary lymphoma.
Ten patients with primary pulmonary lymphoma were treated surgically and their clinical characteristics, the experiences of clinical diagnosis and surgical treatment were analyzed. The tumors located in left upper lobe in 2, left lower lobe in 1, right upper lobe in 3, right middle lobe in 3 and right lower lobe in 1. The main symptoms were cough and (or) hemoptysis. Imageological representations (X-ray and CT scanning of thorax) were similar to primary pulmonary carcinoma. Broncho-fibroscopic examination was performed on all cases with negative findings. Eight cases were mistakenly diagnosed as primary pulmonary carcinoma by imageological representations. Only 2 cases were diagnosed as primary pulmonary lymphoma by percutaneous needle biopsy and pathologic examination. All cases received pneumonectomy, ipsilateral hilar and mediastinal lymphadenectomy. All cases with non-Hodgkin's lymphoma received regular chemotherapy (MOPP and ABVD scheme for 1 case with Hodgkin's disease respectively, CHOP for 8 cases with non-Hodgkin's lymphoma), and 3 cases received radiotherapy postoperatively.
Eight cases were non-Hodgkin's lymphoma (B-type) and 2 cases were Hodgkin's disease (mixed type) confirmed by pathological examination. Six cases with non-Hodgkin's lymphoma (3 cases for stage IE, 2 cases for stage II 1E, and 1 case for stage II 2E W) had been surviving for 18-42 months until the follow-up. Two cases with non-Hodgkin's lymphoma (stage II 2E, B-cell, low-grade) and 2 cases with Hodgkin's disease (stage IE and II 2E, mixed type) died in 24, 32, 8 and 17 months postoperatively respectively.
Primary pulmonary lymphoma is a rare type of malignant lung neoplasm without special clinical features. The preoperative diagnosis is difficult. Treatment modalities include surgical treatment, radiotherapy and regular chemotherapy postoperatively.
探讨原发性肺淋巴瘤的临床特点、诊断及外科治疗原则。
对10例原发性肺淋巴瘤患者进行手术治疗,分析其临床特点、临床诊断及外科治疗经验。肿瘤位于左上叶2例,左下叶1例,右上叶3例,右中叶3例,右下叶1例。主要症状为咳嗽和(或)咯血。影像学表现(胸部X线及CT扫描)与原发性肺癌相似。所有病例均行纤维支气管镜检查,结果均为阴性。8例因影像学表现被误诊为原发性肺癌。仅2例经皮肺穿刺活检及病理检查确诊为原发性肺淋巴瘤。所有病例均行肺叶切除及同侧肺门和纵隔淋巴结清扫术。所有非霍奇金淋巴瘤患者均接受正规化疗(1例霍奇金病分别采用MOPP和ABVD方案,8例非霍奇金淋巴瘤采用CHOP方案),3例术后接受放疗。
病理检查确诊8例为非霍奇金淋巴瘤(B型),2例为霍奇金病(混合型)。6例非霍奇金淋巴瘤(IE期3例,II 1E期2例,II 2E W期1例)随访至18 - 42个月仍存活。2例非霍奇金淋巴瘤(II 2E期,B细胞,低级别)和2例霍奇金病(IE期和II 2E期,混合型)分别于术后24、32、8和17个月死亡。
原发性肺淋巴瘤是一种罕见的肺部恶性肿瘤,无特殊临床特征,术前诊断困难。治疗方式包括手术治疗、放疗及术后正规化疗。