论文部分内容阅读
嗜酸粒细胞增生性淋巴肉芽肿,是一种少见的疾病,至今国内仅报道86例。我院于1984年1月至1985年12月门诊观察治疗一例,现报道如下: 患者:李×,男,29岁,已婚,宁夏籍,农民,因全身淋巴结肿大一年余,于1984年1月来诊。患者一年前发现左耳前淋巴结肿大,伴全身皮疹及瘙痒,继而耳后、颈部、颌下、腋下,腹股沟等处淋巴结亦逐渐肿大,曾于1983年9月在某院就诊,骨髓穿刺报告“嗜酸粒细胞增多”,淋巴结活检病理报告为嗜酸粒细胞增多性淋巴肉芽肿,用强
Eosinophilic lymphogranuloma, is a rare disease, so far only reported in 86 cases. Our hospital from January 1984 to December 1985 outpatient observation and treatment of a case, are reported as follows: Patients: Li ×, male, 29 years old, married, Ningxia, peasants, due to systemic lymphadenopathy more than a year, in 1984 January to the clinic. Patients found a year ago, left anterior lymphadenopathy, with systemic rashes and itching, then the ear, neck, submandibular, armpit, groin and other lymph nodes also gradually enlarged, in September 1983 in a hospital , Bone marrow puncture report “eosinophilia”, lymph node biopsy pathology report for eosinophilic lymphogranuloma, with strong