论文部分内容阅读
嗜酸性淋巴肉芽肿是一种较少见的血液系统疾病,现报道1例:赵某,男,33岁,因低热颈部肿块于1988年1月28日来院诊治。2年前发现颈部长“疙瘩”伴低热,质韧不痛,局部有瘙痒感,肿块时大时小,服消炎药后似有缩小,曾去某医院按淋巴结核服抗痨药物治疗,疗效不明著,后又去某医院行局部肿块切除,术后不久复发。查体:一般可,突眼征,左颈部以腮腺为中心10×12不规则肿块,质坚韧,不活动,压痛(±),耳前及腹股沟可见大
Eosinophilic lymphogranuloma is a rare blood disease, is reported in 1 case: Zhao, male, 33 years old, because of low-neck mass in January 28, 1988 to hospital for treatment. 2 years ago found that the neck long “pimple” with low heat, tough quality pain, local sense of itching, when the tumor is small, anti-inflammatory drugs seem to have reduced, had to go to a hospital by lymph node drug anti-tuberculosis treatment, Efficacy unknown, and then go to a hospital local mass excision, recurrence soon after surgery. Physical examination: the general can be, prominent signs of levy, the left neck to the parotid as the center of 10 × 12 irregular mass, tough, inactive, tenderness (±), before the ear and groin can be seen large