Marsh M N, Miller V
J Pediatr Gastroenterol Nutr. 1985 Dec;4(6):931-5. doi: 10.1097/00005176-198512000-00013.
The mitotic activity of epithelial lymphocytes (expressed as percentage mitotic figures/3,000 lymphocytes/mucosal biopsy) was determined in a random sample of jejunal biopsies performed on 44 children with malabsorption, diarrhoea, or failure to thrive. The mitotic index (MI) exceeded 0.2% in 19 biopsies obtained from children with untreated celiac sprue (CS); there were no false positives. The remaining 25 biopsies (MI of less than 0.2%) were considered to be "nonceliac" in origin, among which were several with a severe degree of villous flattening. Conditions in this latter category excluded by a low MI included cow's milk protein enteropathy, selective immunoglobulin A deficiency, combined variable immunodeficiency, Crohn's jejunitis, and intractable diarrhoea of infancy. A high MI (greater than 0.2%) prospectively distinguishes mucosal lesions due to untreated CS from other causes of malabsorption, particularly those associated with villous flattening, but in which the MI is less than 0.2%. This index is therefore proposed as a simple, reliable, and prospective histological marker of CS, and one that could: reduce the need to perform multiple biopsies during a gluten-free diet; and avoid the necessity for follow-up "diagnostic" gluten challenges, especially in very young children.
对44名患有吸收不良、腹泻或发育不良的儿童进行空肠活检的随机样本,测定上皮淋巴细胞的有丝分裂活性(以有丝分裂图像百分比/3000淋巴细胞/黏膜活检表示)。在从未经治疗的乳糜泻(CS)患儿获得的19份活检样本中,有丝分裂指数(MI)超过0.2%;无假阳性结果。其余25份活检样本(MI小于0.2%)被认为起源于“非乳糜泻”,其中几份有严重程度的绒毛萎缩。MI低排除在后者类别中的情况包括牛奶蛋白肠病、选择性免疫球蛋白A缺乏症、联合可变免疫缺陷、克罗恩空肠炎和婴儿顽固性腹泻。高MI(大于0.2%)可前瞻性地区分未经治疗的CS引起的黏膜病变与其他吸收不良原因,特别是那些与绒毛萎缩相关但MI小于0.2%的原因。因此,该指数被提议作为CS的一种简单、可靠且前瞻性的组织学标志物,它可以:减少在无麸质饮食期间进行多次活检的需求;避免进行后续“诊断性 ”麸质激发试验的必要性,尤其是在非常年幼的儿童中。