Nair Ahalya, Ponnusamy Madhusudhanan
Department of Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Additional Professor & Head of Department, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, India.
Indian J Nucl Med. 2024 May-Jun;39(3):163-169. doi: 10.4103/ijnm.ijnm_127_23. Epub 2024 Aug 17.
Cholescintigraphy using Tc-99m Mebrofenin is routinely performed as an initial diagnostic test in infants with neonatal cholestasis suspected of having biliary atresia. Demonstration of drainage of bile into the small intestine indicates patency of the biliary tract and thus rules out biliary atresia. Non-excretion of tracer into the small intestine, however, can be caused by obstructive as well as non-obstructive conditions, and it is known that false-positive findings are found with the use of Tc-99m Mebrofenin scintigraphy.
In the present study, we retrospectively calculated the proportion of infants eventually diagnosed to have biliary atresia that were initially ruled to have a non-excreting cholescintigraphy pattern in our institution. We have also attempted a systematic description of the cardinal histological characteristics, haematological and hepatic biochemical variables in infants with non-excreting patterns.
This retrospective, descriptive study was conducted in Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry. We reviewed data from infants who underwent cholescintigraphy with Tc-99m Mebrofenin between January 2016 through June 2022. We included infants in whom the scan was ruled "non-excreting" i.e. those infants in whom biliary atresia could not be ruled out based on the results of the scan. The difference in mean for haematological parameters and ALP were compared between the two groups i.e., biliary atresia versus other than biliary atresia by using Independent student's t-test; the remaining liver biochemical parameters were compared by using Mann-Whitney U Test and a p value < 0.05 was considered to be statistically significant.
A non-excretory pattern on cholescintigraphy was found to be due to biliary atresia in 49% of cases (as confirmed by exploratory surgery) and an additional 19.6 % of cases by trucut biopsy (total 68.6%). The difference in the mean serum GGT levels was found to be statistically significant (<0.001).
A non-draining pattern on cholescintigraphy is caused by biliary atresia in the greater percentage of cases presenting with cholestasis. The difference in mean GGT levels was found to be statistically significant between biliary atresia and other causes of non-draining patterns on cholescintigraphy.
使用锝-99m 美罗芬宁进行的肝胆闪烁显像通常作为疑似患有胆道闭锁的新生儿胆汁淤积症婴儿的初始诊断测试。胆汁排入小肠的显像表明胆道通畅,从而排除胆道闭锁。然而,示踪剂未排入小肠可能由阻塞性和非阻塞性情况引起,并且已知使用锝-99m 美罗芬宁闪烁显像会出现假阳性结果。
在本研究中,我们回顾性计算了在我们机构中最初被判定为肝胆闪烁显像无排泄模式但最终被诊断为患有胆道闭锁的婴儿比例。我们还尝试系统描述无排泄模式婴儿的主要组织学特征、血液学和肝脏生化变量。
这项回顾性描述性研究在本地治里的贾瓦哈拉尔研究生医学教育与研究学院(JIPMER)进行。我们回顾了 2016 年 1 月至 2022 年 6 月期间接受锝-99m 美罗芬宁肝胆闪烁显像的婴儿的数据。我们纳入了扫描结果被判定为“无排泄”的婴儿,即那些根据扫描结果不能排除胆道闭锁的婴儿。通过独立样本 t 检验比较两组(即胆道闭锁组与非胆道闭锁组)血液学参数和碱性磷酸酶(ALP)的平均差异;其余肝脏生化参数通过 Mann-Whitney U 检验进行比较,p 值<0.05 被认为具有统计学意义。
在 49%的病例中(经探查手术证实),肝胆闪烁显像的无排泄模式是由胆道闭锁引起的,另外 19.6%的病例通过 Trucut 活检确诊(总计 68.6%)。发现血清γ-谷氨酰转移酶(GGT)水平的平均差异具有统计学意义(<0.001)。
在胆汁淤积症患者中,大部分病例的肝胆闪烁显像无引流模式是由胆道闭锁引起的。发现胆道闭锁与肝胆闪烁显像无引流模式的其他原因之间的平均 GGT 水平差异具有统计学意义。