“无分泌型”多发性骨髓瘤系骨髓瘤中少见的一种类型,仅占该病的1～2％。国内文献报道不多。“无分泌型”多发性骨髓瘤并髓外浆细胞瘤国内尚未见报道,国外亦属少见。现将我院收治的1例报道如下。 患者男性,44岁,农民,因胸廓疼痛、头昏、乏力5个月,于1984年5月30日入院。 患者因胸廓疼痛逐渐加重,伴头昏乏力、面色苍白二个月,就诊于当地医院。该院检查发现血沉降率高、贫血,但胸部及颅骨X线照片未发现异常。骨髓检查符合“多发性骨髓瘤”的诊断,应用COP方案一疗 A rare type of “non-secreting” multiple myeloma line of myeloma, accounting for only 1 to 2% of the disease. Domestic literature reported little. “Secretion-free” multiple myeloma and extramedullary plasmacytoma have not been reported in China, foreign countries are also rare. Now in our hospital one case reported as follows. Male patient, 44 years old, farmer, due to chest pain, dizziness, fatigue for 5 months, was admitted on May 30, 1984. Patients gradually aggravated by thoracic pain, accompanied by dizziness, pale for two months, visited a local hospital. The hospital found that high blood sedimentation rate, anemia, but no abnormal chest and skull X-ray findings. Bone marrow examination in line with “multiple myeloma” diagnosis, the application of COP regimen