Halaby H, Bakheet S M, Shabib S, Powe J E, Al Mehaidib A, Nazer H
Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
J Nucl Med. 2000 Feb;41(2):215-9.
Protein-losing enteropathy (PLE) can be diagnosed scintigraphically using 99mTc-human serum albumin (HSA) scans.
To evaluate the usefulness of this method in detecting enteric protein loss, we retrospectively reviewed the 99mTc-HSA scans of 18 children presenting consecutively with PLE.
Enteric 99mTc-HSA uptake was noted in 12 patients (8 boys, 4 girls) with a mean age of 7.4 y. Early dynamic images showed abdominal uptake that was most likely in the small bowel in 91% of the scans. Delayed images showed abnormal accumulation that was localized in the colon in 73% and in the small bowel in 27% of the scans. A 4-mo follow-up scan obtained in 3 patients showed reduced HSA uptake after a high-protein, low-fat, medium-chain triglyceride oil-based diet and fat-soluble vitamins. Mean serum albumin, total protein, gammaglobulin, and calcium levels were significantly decreased. Ten patients (from 4 families) were diagnosed to have primary intestinal lymphangectasia. One patient had active Salmonella enterocolitis, and 1 had giardiosis. 99mTc-HSA was normal in the remaining 6 patients (3 boys, 3 girls) with a mean age of 3.5 y (range, 2-5 y). Mean serum albumin, total protein, gammaglobulin, and calcium levels were less decreased than those of the first group. Five of these patients had primary intestinal lymphangactesia (associated with infantile systemic hyalinosis in 1 patient). The remaining patient had normal duodenal biopsy, and the cause of protein loss remained unknown.
The 99mTc-HSA scan is useful in the evaluation of children with PLE, especially those with severe hypoproteinemia and hypoalbuminemia, presumably reflecting a high rate of protein loss.
蛋白丢失性肠病(PLE)可通过99mTc - 人血清白蛋白(HSA)扫描进行闪烁显像诊断。
为评估该方法在检测肠道蛋白丢失中的实用性,我们回顾性分析了18例连续出现PLE的儿童的99mTc - HSA扫描结果。
12例患者(8例男孩,4例女孩)出现肠道99mTc - HSA摄取,平均年龄7.4岁。早期动态图像显示91%的扫描中腹部摄取最可能位于小肠。延迟图像显示73%的扫描中异常积聚位于结肠,27%位于小肠。3例患者进行的4个月随访扫描显示,在高蛋白、低脂、中链甘油三酯油基饮食和脂溶性维生素治疗后,HSA摄取减少。平均血清白蛋白、总蛋白、γ球蛋白和钙水平显著降低。10例患者(来自4个家庭)被诊断为原发性肠淋巴管扩张症。1例患者患有活动性沙门氏菌肠炎,1例患有贾第虫病。其余6例患者(3例男孩,3例女孩)平均年龄3.5岁(范围2 - 5岁),99mTc - HSA扫描结果正常。其平均血清白蛋白、总蛋白、γ球蛋白和钙水平降低程度低于第一组。其中5例患者患有原发性肠淋巴管扩张症(1例与婴儿系统性透明变性相关)。其余患者十二指肠活检正常,蛋白丢失原因不明。
99mTc - HSA扫描有助于评估PLE患儿,尤其是那些患有严重低蛋白血症和低白蛋白血症的患儿,可能反映了高蛋白丢失率。