Mukhopadhyay Sabuj Ghana, Roy Paromita, Chatterjee Uttara, Datta Chhanda, Banerjee Mala, Banerjee Sugato, Basu Ashoke Kumar, Ganguli Manojit
Department of Pathology, Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
Indian J Pathol Microbiol. 2014 Jul-Sep;57(3):380-5. doi: 10.4103/0377-4929.138722.
Biliary atresia (BA) is a destructive process affecting both extra- and intra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tree and cirrhosis usually within 2 years. Factors influencing the outcome of portoenterostomy (PE) have not been clearly defined.
Our aim was to identify children with no evidence of liver disease 10 years or more after PE and to compare the pathology of liver and biliary remnants in this group with those associated with poor outcome.
Prospective observational study.
Wedge biopsies of liver and portal remnants, taken at the time of PE, where available, were reviewed. The parameters studied were - presence of large bile ducts (>150 μ), degree of fibrosis and bile duct proliferation (BDP), presence of ductal plate malformation (DPM) and age at operation.
Fisher's exact test with Freeman Halton extension for univariate analysis and Logistic regression analysis as multivariate analysis.
Of 68 cases operated between 1995 and 2001, 14 patients survived >10 years and 54 were associated with poor outcome. Large ducts were significantly more in survivors (70% vs. 26%, P = 0.02). DPM was not seen in any of the survivors and was present in 24% of poor outcome group. Fibrosis and BDP were also significantly less among the survivors (P < 0.001, P = 0.03, respectively). The mean ages at operation in the two groups were 66.8 and 89.6 days, respectively.
From this study, we feel that lower degree of fibrosis and BDP, absence of DPM, presence of large ducts and younger age at operation were associated with better long-term outcome. Of these, degree of fibrosis was the most significant factor.
胆道闭锁(BA)是一种破坏性疾病,可影响肝内外胆管,通常在2年内导致胆管树纤维化、闭塞及肝硬化。影响肝门空肠吻合术(PE)预后的因素尚未明确界定。
我们的目的是确定在PE术后10年或更长时间内无肝病证据的儿童,并将该组患儿的肝脏和胆道残余组织病理学与预后不良者进行比较。
前瞻性观察研究。
回顾性分析PE手术时获取的肝脏楔形活检标本及肝门残余组织(若有)。研究参数包括:大胆管(>150μm)的存在情况、纤维化程度和胆管增生(BDP)、导管板畸形(DPM)的存在情况及手术年龄。
单因素分析采用带Freeman Halton扩展的Fisher精确检验,多因素分析采用Logistic回归分析。
1995年至2001年间接受手术的68例患儿中,14例存活超过10年,54例预后不良。存活者中大胆管明显更多(70%对26%,P = 0.02)。所有存活者均未发现DPM,而预后不良组中24%存在DPM。存活者的纤维化和BDP也明显较少(分别为P < 0.001,P = 0.03)。两组的平均手术年龄分别为66.8天和89.6天。
通过本研究,我们认为纤维化程度和BDP较低、无DPM、存在大胆管以及手术年龄较小与更好的长期预后相关。其中,纤维化程度是最显著的因素。