日本胸部疾患学会雑誌
Online ISSN : 1883-471X
Print ISSN : 0301-1542
ISSN-L : 0301-1542
胸水中より異型形質細胞とM蛋白を証明したIgG, λ型多発性骨髄腫の1例
福嶋 和文石見 寿康筒井 大八森岡 茂治西村 良秋田中 立夫
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1979 年 17 巻 7 号 p. 415-420

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Pulmonary involvement in multiple myeloma is very uncommon. In the case to be presented, extraosseous pleuropulmonary involvement was a dominant feature.
A 69-year-old man, a farmer, was admitted to our hospital with a chief complaint of anorexia on August 21.1978. A test for Bence Jones protein was positive. The erythrocyte sedimentation rate was 66mm/hr. The serum total protein was 8.1g/dl and a monoclonal pattern was observed in γ-globulin area. X-ray films of the bones showed generalized osteoporosis and punched-out lesions in the skull. X-ray films of the chest revealed a mass with an ill-defined margin in the right hilar region, measuring 3×3.5cm in its greatest dimensions, extrapleural signs associated with pleural fluid in the left lung field, and also polycystic shadows in the left lower lung field. A lot of myeloma cells and M-protein were revealed in the pleural fluid. The patient was diagnosed as IgG, λ-type multiple myeloma on immunoelectrophoretic examination of the serum, urine, and pleural fluid. Treatment with corticosteroids and cyclophosphamide was quite ineffective and he died in 2 months.

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