作者报告一例24岁、男性、空肠上段10 Cm长范围僵直破坏,肠壁增厚达4 Cm以上,病理检查为非白血病性淋巴瘤(Burkitt′s Lymphoma)合并有整个小肠淋巴滤泡增生和γ球蛋白异常血症。γ球蛋白异常血症合并小肠淋巴滤泡增生最早于1966年就报告过8例,主要表现为γ球蛋白异常(γ球蛋白减少,IgG中度减少,IgA缺如,IgM缺如或接近缺如),小肠淋巴滤泡增生,呼吸道感染的易感性增加,间歇性或慢性腹泻,有时可伴有轻度脂肪泻,以及鞭毛虫感染。无明显的遗传因 The authors report a 24-year-old male with a 10 cm long stiff destruction of the upper jejunum and a bowel wall thickening of more than 4 cm. The pathological examination was a combination of whole small intestinal lymphofibroblasts and γ Aberrant hemoglobin. Gammaglobulic anomalies with intestinal lymphoid follicular hyperplasia were reported as early as 1966, 8 cases were reported, mainly as γ-globulin abnormalities (γ-globulin decreased, moderate reduction of IgG, IgA lack of IgM missing or near the lack of Eg, small bowel lymphatic follicular hyperplasia, increased susceptibility to respiratory infections, intermittent or chronic diarrhea, sometimes associated with mild steatorrhea, and flagellate infections. No obvious genetic causes