Cervetto J L, Ramonet M, Nahmod L H, Gallardo F
Pediatric Division, Prof. Alejandro Posadas National Hospital, Haedo, Buenos Aires, Argentina.
Arq Gastroenterol. 1987 Apr-Jun;24(2):102-12.
Fourteen patients between the ages of 9 months and 5 years with chronic diarrhea and giardiasis were studied. Ten were eutrophic and 4 undernourished. The parasitological diagnosis was based on stool examination, a trophozoite search in duodenal aspiration, mucus adhered to mucosa and parasite identification in the intestinal biopsy material. Functional intestinal absorption studies, IgA determination in intestinal secretions and immunofluorescence studies were made. After the tests, tinidazole in suspension was administered at 60-70 mg/kg in one single oral dose. Patients were clinically re-evaluated and tests were done again after 30 days. The purpose of this paper was to evaluate the changes in the functional morphologic and immunologic studies and the therapeutic efficacy of the drug in a single dose. Nine patients had good clinical results, 2 fair and 3 were not evaluated due to celiac disease. All had negative results on the parasitological tests after treatment. There was no relationship between the number of parasites and the severity of symptoms. There was no significant difference between stool fat and d-xylose at the time of diagnosis and 30 days after the administration of tinidazole. The lactose tolerance test presented a significant difference (p less than 0.05) in the disaccharide absorption after treatment. The secretory IgA revealed significantly lower value (p less than 0.01) with respect to the normal values. The immunofluorescence showed productive IgA cells in all cases. The histologic changes were: mild enteropathy (grade I) in 6 patients; moderate (grade II) in 5; and severe (grade III-IV) in 3. Improvement of the mucosa was seen in 6 patients.
对14名年龄在9个月至5岁之间患有慢性腹泻和贾第虫病的患者进行了研究。其中10名营养良好,4名营养不良。寄生虫学诊断基于粪便检查、十二指肠抽吸物中滋养体的查找、黏膜附着的黏液以及肠道活检材料中寄生虫的鉴定。进行了肠道功能吸收研究、肠道分泌物中IgA的测定以及免疫荧光研究。检测后,以60 - 70毫克/千克的剂量单次口服给予替硝唑混悬液。对患者进行临床重新评估,并在30天后再次进行检测。本文的目的是评估单次给药后功能形态学和免疫学研究的变化以及该药物的治疗效果。9名患者临床效果良好,2名一般,3名因乳糜泻未进行评估。治疗后所有患者的寄生虫学检测结果均为阴性。寄生虫数量与症状严重程度之间无关联。诊断时与给予替硝唑30天后,粪便脂肪和d - 木糖之间无显著差异。乳糖耐受试验显示治疗后双糖吸收有显著差异(p小于0.05)。分泌型IgA相对于正常值显著降低(p小于0.01)。免疫荧光显示所有病例中均有产生IgA的细胞。组织学变化为:6名患者为轻度肠病(I级);5名为中度(II级);3名为重度(III - IV级)。6名患者的黏膜有改善。