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[原发性肺淋巴瘤:18例分析]

[Primary pulmonary lymphoma: analysis of 18 cases].

作者信息

Tian Xin-Lun, Feng Rui-E, Shi Ju-Hong, Duan Ming-Hui, Wang Jing-Lan, Liu Hong-Rui, Cai Bo-Qiang, Gao Jin-Ming, Xu Wen-Bing, Zhu Yuan-Jue

机构信息

Department of Respiratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2008 Jun;31(6):401-5.

Abstract

OBJECTIVE

To study the clinical characteristics, pathology, diagnosis and treatment of primary pulmonary lymphoma.

METHODS

Eighteen cases of primary pulmonary lymphoma diagnosed from Jan 1989 to Feb 2007 were retrospectively analyzed.

RESULTS

There were 6 males and 12 females, with a median age of 47.5 years (17-71 years). Fifteen cases were diagnosed by surgical lung biopsy; 1 by percutaneous needle lung biopsy (1/6), 1 by percutaneous needle lung biopsy and bronchoscopic examination at the same time, the other 1 by bronchoscopic examination (1/10). Histological diagnosis showed that 2 cases were Hodgkin lymphoma, 9 mucosa-associated lymphoid tissue lymphoma, 1 follicular lymphoma, 2 diffuse large B cell lymphoma 2 anaplastic large cell lymphoma, 2 non-Hodgkin lymphoma whichcould not be classified because the slides were from other hospitals. The most common symptoms were cough (9/18) and fever (6/18). ESR elevation was common (10/12). CT features included solitary or multiple nodules (14/18), patchy opacities (11/18), consolidations (5/18), pleural effusions (5/18), atelectasis (5/18), and cavities (1/18). Misdiagnosis was found in 11 patients. Treatment modalities included surgical resection, radiotherapy and chemotherapy. Median follow-up time was 11 months (10 d to 205 mon). Thirteen patients were still alive, 4 patients were lost, and 1 patient died. The prognosis was associated with the level of [25.1 x 10(9)/L(18.1 - 39. -1) x 10(9)/L in poor prognosis group, 6.7 x 10(9)/L (5.48 - 8.41) x 10(9)/L in good prognosis group, u = 0.000, P <0.05] leukocytosis (3/3 vs 1/10, P <0.05).

CONCLUSIONS

The clinical manifestations of primary pulmonary lymphoma are nonspecific. Misdiagnosis is common. Surgical lung biopsy is necessary for early diagnosis.

摘要

目的

研究原发性肺淋巴瘤的临床特征、病理、诊断及治疗。

方法

回顾性分析1989年1月至2007年2月确诊的18例原发性肺淋巴瘤病例。

结果

男性6例,女性12例,中位年龄47.5岁(17 - 71岁)。15例经手术肺活检确诊;1例经皮肺穿刺活检确诊(1/6),1例同时经皮肺穿刺活检及支气管镜检查确诊,另1例经支气管镜检查确诊(1/10)。组织学诊断显示,2例为霍奇金淋巴瘤,9例为黏膜相关淋巴组织淋巴瘤,1例为滤泡性淋巴瘤,2例为弥漫性大B细胞淋巴瘤,2例为间变性大细胞淋巴瘤,2例因玻片来自其他医院无法分类的非霍奇金淋巴瘤。最常见症状为咳嗽(9/18)和发热(6/18)。血沉升高常见(10/12)。CT表现包括孤立或多发结节(14/18)、斑片状模糊影(11/18)、实变(5/18)、胸腔积液(5/18)、肺不张(5/18)及空洞(1/18)。11例患者存在误诊。治疗方式包括手术切除、放疗及化疗。中位随访时间为11个月(10天至205个月)。13例患者存活,4例失访,1例死亡。预后与白细胞增多水平相关(预后不良组[25.1×10⁹/L(18.1 - 39. -1)×10⁹/L,预后良好组6.7×10⁹/L(5.48 - 8.41)×10⁹/L,u = 0.000,P <0.05])(3/3 vs 1/10,P <0.05)。

结论

原发性肺淋巴瘤的临床表现无特异性。误诊常见。手术肺活检对早期诊断必要。

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