Kasai Portoenterostomy, Successful Liver Transplantation, and Immunosuppressive Therapy for Biliary Atresia in a Female Baby: A Case Report

被引:0
|
作者
Shan, Liang [1 ,3 ,4 ]
Wang, Fengling [1 ]
Zhai, Dandan [1 ]
Meng, Xiangyun [1 ]
Liu, Jianjun [1 ]
Lv, Xiongwen [2 ,4 ]
机构
[1] Anhui Med Univ, Peoples Hosp Hefei 2, Hefei Hosp, Dept Pharm, Hefei 230011, Anhui, Peoples R China
[2] Anhui Med Univ, Anhui Prov Key Lab Major Autoimmune Dis, Hefei 230032, Anhui, Peoples R China
[3] Anhui Med Univ, Inflammat & Immune Mediated Dis Lab Anhui Prov, Hefei 230032, Anhui, Peoples R China
[4] Anhui Med Univ, Key Lab Major Autoimmune Dis, Hefei 230032, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
biliary atresia; Kasai portoenterostomy; living-related liver transplantation; immunosuppressive drug; therapeutic drug monitoring; ONCE-DAILY FORMULATION; TACROLIMUS; CYCLOSPORINE; PATHOGENESIS; PROPHYLAXIS; REJECTION; FIBROSIS; OUTCOMES;
D O I
10.2147/JIR.S432024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Biliary atresia (BA) is a severe neonatal progressive cholangiopathy of unknown etiology. A timely Kasai portoenterostomy (KPE) improves survival of the native liver in patients with BA, although liver transplantation remains the ultimate treatment for most (60%-80%) patients. However, postoperative adverse effects of liver transplantation may be significant. In addition, patients require lifelong immunosuppressive therapy after liver transplantation. Case Summary: Here, we report a case of a newborn female baby (birthday: 10-03-2018) with congenital BA (confirmed at 76 days of life) who survived KPE (first surgery at 85 days of life) and underwent successful living-related liver transplantation (LRLT) (second surgery at 194 days of life). Additionally, we reviewed the existing literature on BA. After KPE (at 85 days of life), the liver function of the baby did not improve, and the indicators of liver and kidney function showed a trend of aggravation, indicating that the liver function had been seriously damaged before KPE (at 85 days of life), demonstrating the urgent need for liver transplantation surgery. The female baby survived after part of her father's liver was successfully transplanted into her body (at 194 days of life). The patient recovered successfully. No other diseases were found at the 4-year follow-up, and all indices of liver and kidney functions tended to be normal. Conclusion: This case highlights the following. Postoperative alkaline phosphatase was consistently above the normal range, although the reason for this was unclear; neither tacrolimus nor cyclosporine A has formulations designed specifically for infants, which does not meet the needs of clinical individualized medication, suggesting that these anti-rejection drugs are future development directions. Only one case of congenital BA has been found thus far in Hefei, and this case has extremely important reference significance for the prevention, treatment, and diagnosis of BA in Hefei, Anhui province.
引用
收藏
页码:4905 / 4920
页数:16
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