论文部分内容阅读
原始免疫细胞性淋巴腺瘤或血管原始免疫细胞性淋巴腺瘤伴异常蛋白血症(AILD)是一种最近才被认识的非肿瘤性淋巴增生性疾病,作者报导4例淋巴管造影和1例超声图检查的结果。5例患者中,男性3例,女性2例,平均年龄67岁(范围59～78岁)。发病前有上呼吸道感染及胆囊切除术各1例。临床症状分别为发热、出汗、不适、中度贫血、体重减轻、肝脾肿大和皮疹,最突出的是均有全身性淋巴结肿大;1例为巨大的上腹部肿块。4例多无性繁殖系两种球蛋白病(包括1例多无性繁殖系高两种球蛋白血症),1例还有IgA和IgG增高。4例胸片正常,1例示支气管旁和双侧支气管肺淋巴结肿大,1例钡餐检查和尿路造影
Primary immunocytic lymphomas or primary prolymphocytoma with abnormal proteinuria (AILD) is a newly recognized non-neoplastic lymphoproliferative disease. The authors reported 4 lymphangiomas and 1 case Ultrasound examination results. Among 5 patients, there were 3 males and 2 females, with an average age of 67 years (range, 59-78 years). Before the onset of upper respiratory tract infection and cholecystectomy in 1 case. Clinical symptoms were fever, sweating, discomfort, moderate anemia, weight loss, hepatosplenomegaly and rash, the most prominent are both systemic lymphadenopathy; a case of a huge upper abdominal mass. Four polygenic clones had two globulin diseases (including one polygamous with two hypergammaglobulinemia), and one had increased IgA and IgG. 4 cases of normal chest, 1 case of bronchial and bilateral bronchial lymph nodes, 1 case of barium meal examination and urography