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两例肺瓦尔登斯特伦巨球蛋白血症

Two cases of pulmonary Waldenström's macroglobulinemia.

作者信息

Kobayashi H, Ii K, Hizawa K, Maeda T

出版信息

Chest. 1985 Aug;88(2):297-9. doi: 10.1378/chest.88.2.297.

Abstract

Two cases of Waldenström's macroglobulinemia (WMG) with principally pulmonary manifestation are presented. The disease in both cases was discovered from abnormal shadow in chest x-ray films, without classic features of the disease such as anemia, lymphadenopathy, hepatosplenomegaly or visual disturbance. Transbronchial biopsy (case 1) and open lung biopsy (case 2) revealed diffuse infiltration of lymphoplasmacytoid cells. In both cases, the cytoplasm of proliferating cells stained for monoclonal IgM by the peroxidase-antiperoxidase method. Immunologic examination revealed that almost all tumor cells obtained from bronchoalveolar lavage fluid (case 1) and cell suspension of the right lung (case 2) had monoclonal surface immunoglobulin for IgM. These data established the diagnosis of pulmonary WMG. These cases indicate the importance of immunologic studies for establishing a diagnosis of pulmonary WMG, since histologic findings in biopsy specimens and clinical features are often not specific enough for making this diagnosis.

摘要

本文报告两例以肺部表现为主的华氏巨球蛋白血症(WMG)。两例患者均因胸部X线片出现异常阴影而被发现患有此病,均无该疾病的典型特征,如贫血、淋巴结病、肝脾肿大或视觉障碍。经支气管活检(病例1)和开胸肺活检(病例2)显示淋巴细胞浆细胞样细胞弥漫性浸润。在两例病例中,增殖细胞的胞质通过过氧化物酶-抗过氧化物酶法对单克隆IgM染色。免疫检查显示,从支气管肺泡灌洗液(病例1)和右肺细胞悬液(病例2)中获得的几乎所有肿瘤细胞均具有针对IgM的单克隆表面免疫球蛋白。这些数据确立了肺部WMG的诊断。这些病例表明免疫研究对于确立肺部WMG诊断的重要性,因为活检标本的组织学发现和临床特征往往不够特异,不足以做出该诊断。

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