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
Department of Respiratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2008 Jun;31(6):401-5.
To study the clinical characteristics, pathology, diagnosis and treatment of primary pulmonary lymphoma.
Eighteen cases of primary pulmonary lymphoma diagnosed from Jan 1989 to Feb 2007 were retrospectively analyzed.
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).
The clinical manifestations of primary pulmonary lymphoma are nonspecific. Misdiagnosis is common. Surgical lung biopsy is necessary for early diagnosis.
研究原发性肺淋巴瘤的临床特征、病理、诊断及治疗。
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。
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)。
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。