Hjelt K, Paerregaard A, Krasilnikoff P A
Børneafdelingen, Københavns Amts Sygehus i Gentofte.
Ugeskr Laeger. 1993 Dec 13;155(50):4083-6.
During a six-year period, 29 children (aged 0.7-13.5 years, mean 3.3 years) suffering from chronic diarrhoea due to giardiasis were studied. The incidence of this illness was 81 per 1,000,000 per year among children aged 0- < 7 years. According to growth charts, relative height and weight of the patients decreased significantly (both approximately 0.5 SD) from before the onset of diarrhoea to the time of diagnosis and subsequently increased up to the end of catch-up growth. Small intestinal mucosal specimens were studied. Two patients had severe villous atrophy, 8 moderate abnormalities, 6 only slight changes and 13 biopsies were normal. D-xylose or lactose malabsorption was detected in 25% of the patients. The lactose malabsorption was due to hereditary low lactase levels. None of the patients with a Danish ethnic background showed lactose malabsorption. D-xylose absorption and the relative weight loss of the patients correlated with the degree of mucosal damage. Patients with persistent diarrhoea (n = 19) were younger and had a shorter duration of diarrhoeal illness and a more significant weight reduction than those with intermittent diarrhoea (n = 10). However, the age at onset of symptoms was similar in the two groups (medians 1.3 years). Seven patients contracted the disease abroad. They all developed persistent diarrhoea and had a more severe course of the illness than those who acquired the disease in Denmark.
在六年期间,对29名因贾第虫病导致慢性腹泻的儿童(年龄0.7 - 13.5岁,平均3.3岁)进行了研究。在0至<7岁的儿童中,这种疾病的发病率为每年每100万人81例。根据生长图表,患者的相对身高和体重从腹泻发作前到诊断时显著下降(均约0.5标准差),随后在追赶生长结束时增加。对小肠黏膜标本进行了研究。两名患者有严重的绒毛萎缩,8名有中度异常,6名只有轻微变化,13份活检结果正常。25%的患者检测到D - 木糖或乳糖吸收不良。乳糖吸收不良是由于遗传性乳糖酶水平低。没有丹麦族裔背景的患者出现乳糖吸收不良。患者的D - 木糖吸收和相对体重减轻与黏膜损伤程度相关。持续性腹泻患者(n = 19)比间歇性腹泻患者(n = 10)年龄更小,腹泻病程更短,体重减轻更显著。然而,两组症状出现的年龄相似(中位数1.3岁)。7名患者在国外感染该病。他们都出现了持续性腹泻,且病情比在丹麦感染该病的患者更严重。