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血管性原始免疫细胞性淋巴结病(以下简称AIBL)是近年来新认识的淋巴组织增生性疾病,其临床特征为全身淋巴结肿大,肝脾肿大,多株性高球蛋白血症,确诊需要依赖淋巴结活检。我们自1980年至今曾遇到二例,现报告如下: 例1 男性,60岁,农民,住院号2958。因咳嗽咯痰伴全身瘙痒一个月,右上腹疼痛伴发烧4天,于1980年10月入院。入院前一个月开始咳嗽、咯痰、乏力、消瘦、全身瘙痒。近四天来右上腹痛伴体温增
Vascular primitive immunocytic lymphadenopathy (hereinafter referred to as AIBL) is a newly recognized lymphoproliferative disease in recent years, and its clinical features include generalized lymphadenopathy, hepatosplenomegaly, and multiple strains of hypergammaglobulinemia. Rely on lymph node biopsy. We have encountered two cases since 1980 and are reported as follows: Example 1 Male, 60, farmer, hospitalization number 2958. Due to cough, phlegm with systemic itching for a month, right upper quadrant pain with fever for 4 days, admitted in October 1980. One month before admission cough, expectoration, fatigue, weight loss, systemic itching. Right upper quadrant pain accompanied by body temperature increase in the past four days