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Feasibility of domino liver transplantation from hyperhomocsyteinemia
Wei Qu1, Zhi-Jun Zhu1, Lin Wei1
1Liver Transplantation Section, Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Yong'an road, 95, Xicheng District, Beijing, PR China; National Clinical Research Center of Digestive Diseases, Beijing, PR China; Clinical Center for Pediatric Liver Transplantation, Capital Medical University, Beijing, PR China.
Insights
Liver transplantation is effective for treating cystathionine beta synthase (CBS) deficiency, normalizing homocysteine levels. CBS-deficient livers can be safely used for domino transplantation in select recipients.
Area of Science:
- Hepatology
- Metabolic Disorders
- Transplantation Immunology
Background:
- Cystathionine beta synthase (CBS) deficiency causes hyperhomocysteinemia, an autosomal recessive disorder linked to neurological and vascular complications.
- Liver transplantation is rarely reported for CBS deficiency, highlighting a gap in established treatment protocols.
Observation:
- An 8-year-old male with CBS deficiency underwent successful living donor liver transplantation, with normalized homocysteine levels post-surgery.
- The patient's liver was subsequently used for domino transplantation in a recipient with acute liver failure due to cholangiocarcinoma.
Findings:
- The domino recipient developed acquired hyperhomocysteinemia, managed medically, without CBS deficiency-related complications up to 11 months post-transplant.
- The primary recipient experienced an uneventful recovery, demonstrating the efficacy of liver transplantation for CBS deficiency.
Implications:
- Liver transplantation is a safe and effective therapeutic option for patients with CBS deficiency.
- Utilizing livers from CBS-deficient patients for domino transplantation is feasible and beneficial in selected cases, offering a dual therapeutic strategy.
Abstract:
Hyperhomocysteinemia, resulting from a cystathionine beta synthase (CBS) deficiency, is an autosomal recessive disease associated with high levels of homocysteine. Such patients can present with severe mental retardation, ectopia lentis and osteoporosis and thromboembolic disease. To the best of our knowledge, only two cases of liver transplantation for CBS deficiency have been published. Here, we report a case of an 8-year-old male with a CBS deficiency that underwent living donor liver transplantation. The postoperative course was uneventful and homocysteine levels remained normal. The liver of this CBS deficiency patient was then successfully used in domino transplantation. The domino liver transplantation recipient was a 41-year-old male diagnosed with acute liver failure following hemi-liver resection due to cholangiocarcinoma. The domino recipient developed acquired hyperhomocysteinemia, which was controlled with a special regimen of medications. No complications relative to CBS deficiency were observed up to 11 months post-transplant. At this time, the patient expired as a result of cholangiocarcinoma recurrence. In conclusion, our data suggest that liver transplantation for CBS deficiency can be effective, safe and beneficial. It is possible to be both safe and beneficial to use a CBS deficiency patient as a domino donor for salvage liver transplantation in a selective category of recipients.
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