Suppr超能文献

原发性肺非霍奇金淋巴瘤和肺假性淋巴瘤:161例患者的研究

Primary non-Hodgkin's lymphoma and pseudolymphoma of lung: a study of 161 patients.

作者信息

Koss M N, Hochholzer L, Nichols P W, Wehunt W D, Lazarus A A

出版信息

Hum Pathol. 1983 Dec;14(12):1024-38. doi: 10.1016/s0046-8177(83)80258-5.

Abstract

The authors studied 161 cases of primary non-Hodgkin's lymphomas and pseudolymphomas of lung. Small lymphocytic proliferations, which they believe to be lymphomas, constituted 31.6 per cent of cases; plasmacytoid lymphocytic and small cleaved follicular center cell lymphomas (Lukes-Collins system), 22.4 and 11.8 per cent of cases, respectively; and the remaining follicular center cell lymphomas and B-immunoblastic sarcomas, 5.6 per cent of cases. Pseudolymphomas constituted 14 per cent of cases. Most patients were elderly and asymptomatic; in most cases a solitary nodule or infiltrate was observed on a chest radiograph. Radiographic evidence of effusion was found in both lymphomas and pseudolymphomas, but hilar adenopathy was restricted to lymphomas. A few peribronchial reactive germinal centers and intralesional giant cells/granulomas were seen frequently in unequivocal lymphomas, so their presence cannot be used to exclude neoplasia. A generally monomorphic cell population and invasion of bronchial cartilage or visceral pleura are suggestive of malignancy, whereas primitive cytologic appearance and invasion of lymph nodes or parietal pleura are pathognomonic of malignancy. Diffusely admixed mature lymphocytes and plasma cells with numerous reactive follicles suggest pseudolymphomas. Immunologic determination of clonality may be diagnostically definitive. Most localized lesions in lung were treated by surgical resection, whereas in cases of extensive pulmonary disease, biopsies were performed and patients were treated by chemotherapy or irradiation. Both lymphomas and pseudolymphomas recurred, most often within three years. Pseudolymphoma recurred only in lung. When distant spread of lymphoma occurred, it commonly involved extranodal sites. Only 18 of 101 patients with lymphoma died with or of tumor, and no patient with pseudolymphoma died of disease. Neither histologic subtype among the "small cell" lymphoid lymphomas nor the presence of regional node involvement was prognostically significant, but pleural effusion on the initial chest radiograph was a significant predictor of both recurrence and mortality.

摘要

作者研究了161例原发性肺非霍奇金淋巴瘤和肺假淋巴瘤。他们认为属于淋巴瘤的小淋巴细胞增殖性病变占病例的31.6%;浆细胞样淋巴细胞性和小裂滤泡中心细胞淋巴瘤(卢克斯 - 柯林斯分类系统)分别占病例的22.4%和11.8%;其余的滤泡中心细胞淋巴瘤和B免疫母细胞肉瘤占病例的5.6%。假淋巴瘤占病例的14%。大多数患者为老年人且无症状;多数病例在胸部X线片上可见单个结节或浸润影。淋巴瘤和假淋巴瘤均有胸腔积液的影像学证据,但肺门淋巴结肿大仅见于淋巴瘤。在明确的淋巴瘤中常可见一些支气管周围反应性生发中心和病灶内巨细胞/肉芽肿,因此它们的存在不能用于排除肿瘤。细胞群体一般呈单形性以及支气管软骨或脏层胸膜受侵提示为恶性,而原始的细胞学表现以及淋巴结或壁层胸膜受侵则是恶性的特征性表现。弥漫性混合成熟淋巴细胞和浆细胞以及众多反应性滤泡提示为假淋巴瘤。克隆性的免疫测定可能具有诊断决定性意义。肺内大多数局限性病变采用手术切除治疗,而对于广泛肺部疾病的病例,则进行活检并对患者采用化疗或放疗。淋巴瘤和假淋巴瘤均会复发,最常见于3年内。假淋巴瘤仅在肺部复发。淋巴瘤发生远处转移时,通常累及结外部位。101例淋巴瘤患者中只有18例死于肿瘤或因肿瘤死亡,没有假淋巴瘤患者死于该病。“小细胞”淋巴样淋巴瘤中的组织学亚型以及区域淋巴结受累情况在预后方面均无显著意义,但初次胸部X线片上出现胸腔积液是复发和死亡的重要预测指标。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验