Pope R M, Cederbaum A I, Lewis W, Mannik M
Am J Med Sci. 1977 Sep-Oct;274(2):213-9. doi: 10.1097/00000441-197709000-00016.
The clinical course of a patient is described who experienced respiratory insufficiency as the primary manifestation of immunoblastic lymphadenopathy. Respiratory symptoms preceded the enlargement of lymph nodes, improved spontaneously at first and then after steroid therapy. Subsequently these symptoms reappeared concurrent with lymph node enlargement. Hypergammaglobulinemia was noted with marked elevation of polyclonal immunoglobulin M.
本文描述了一名患者的临床病程，该患者以呼吸功能不全作为免疫母细胞性淋巴结病的主要表现。呼吸道症状先于淋巴结肿大出现，起初自行改善，之后经类固醇治疗后好转。随后，这些症状在淋巴结肿大时再次出现。检测到高球蛋白血症，多克隆免疫球蛋白M显著升高。
