Cacciari E, Salardi S, Volta U, Biasco G, Lazzari R, Corazza G R, Feliciani M, Cicognani A, Partesotti S, Azzaroni D
Lancet. 1985 Jun 29;1(8444):1469-71. doi: 10.1016/s0140-6736(85)92251-2.
Duodenal biopsy and tests for antigliadin antibodies were done in 108 children with short stature unassociated with gastrointestinal symptoms. Other investigations for causes of growth failure were also carried out. In 88 patients, the cause of short stature could not be determined (group I). In 9 patients (8.3%) biopsy showed total villous atrophy, indicating probable coeliac disease (group II), while 7 patients had mild partial villous atrophy (group III). 4 patients (3.7%) had complete growth hormone deficiency. Antigliadin antibodies detected by immunofluorescence (IFL-AGA) were positive in 8 of the 9 group II patients. Symptomless coeliac disease is therefore a commoner cause of short stature than is hypopituitarism; by use of the IFL-AGA test it is possible to select patients for biopsy, thereby identifying most of the coeliac patients. If duodenal biopsies had been limited to IFL-AGA positive patients, 18 biopsies would have been carried out and coeliac disease would have been diagnosed in 8 of the 9 patients.
对108名无胃肠道症状的身材矮小儿童进行了十二指肠活检和抗麦胶蛋白抗体检测。还对生长发育迟缓的其他病因进行了检查。88例患者的身材矮小原因无法确定(第一组)。9例患者(8.3%)活检显示全绒毛萎缩,提示可能患有乳糜泻(第二组),而7例患者有轻度部分绒毛萎缩(第三组)。4例患者(3.7%)存在完全性生长激素缺乏。免疫荧光法检测的抗麦胶蛋白抗体(IFL - AGA)在9例第二组患者中有8例呈阳性。因此,无症状性乳糜泻是身材矮小比垂体功能减退更常见的原因;通过使用IFL - AGA检测,可以选择患者进行活检,从而识别出大多数乳糜泻患者。如果十二指肠活检仅限于IFL - AGA阳性患者,那么将进行18次活检,9例患者中有8例将被诊断为乳糜泻。