Yu Young-Dong, Kim Dong-Sik, Yoon Young-In, Park Yong
From the Department of Surgery, Division of HBP Surgery and Liver Transplantation, Korea University Medical Center, Korea University Medical College, Seoul, Korea.
Exp Clin Transplant. 2021 Aug;19(8):880-883. doi: 10.6002/ect.2019.0226. Epub 2021 May 6.
Sinusoidal obstructive syndrome, also known as venoocclusive disease, is a potentially life-threatening complication of hematopoietic stem cell transplant. The conditioning regimens given before hematopoietic stem cell transplant result in the production of toxic metabolites that trigger the activation, damage, and inflammation of the endothelial cells that line the sinusoids. Although liver transplant has been performed for treatment of sinusoidal obstructive syndrome, reports by various liver transplant centers worldwide have been limited and disappointing. We report our experience of successfully treating a patient with sinusoidal obstructive syndrome with deceased donor liver transplant. A 34-year-old male patient was referred to our department due to refractory ascites and jaundice within 1 month after receiving peripheral blood stem cell transplant for acute lymphocytic leukemia. He was diagnosed with biopsy-proven sinusoidal obstructive syndrome. Despite therapy with defibrotide, his condition continued to deteriorate, which included development of intractable pleural effusion, ascites, and progressive renal failure. After undergoing deceased donor liver transplant, the patient's serum bilirubin levels and prothrombin time began to decrease. The histology of the excised liver was compatible with hepatic sinusoidal obstructive syndrome. After being treated for pneumonia, pulmonary edema, and cytomegalovirus viremia, the patient was discharged 2 months after transplant. At 18 months after liver transplant, although he was treated for fungal pneumonia and is being considered for kidney transplant due to unsuccessful weaning from renal replacement therapy, the patient has shown stable liver function and no signs of either graft-versus-host disease or a relapse of acute lymphocytic leukemia. In conclusion, although severe sinusoidal obstructive syndrome in the setting of stem cell transplant has a poor prognosis, we suggest that deceased donor liver transplant should be considered in the treatment of select patients with life-threatening liver dysfunction after hematopoietic stem cell transplant.
窦性阻塞综合征,也称为肝小静脉闭塞病,是造血干细胞移植的一种潜在危及生命的并发症。造血干细胞移植前给予的预处理方案会产生有毒代谢产物,引发肝血窦内衬内皮细胞的激活、损伤和炎症。尽管已进行肝移植治疗窦性阻塞综合征,但全球各肝移植中心的报告有限且令人失望。我们报告了成功用已故供体肝移植治疗一名窦性阻塞综合征患者的经验。一名34岁男性患者因急性淋巴细胞白血病接受外周血干细胞移植后1个月内出现难治性腹水和黄疸而转诊至我科。经活检证实他被诊断为窦性阻塞综合征。尽管使用去纤苷治疗,他的病情仍继续恶化,包括出现难治性胸腔积液、腹水和进行性肾衰竭。在接受已故供体肝移植后,患者的血清胆红素水平和凝血酶原时间开始下降。切除肝脏的组织学检查结果与肝窦性阻塞综合征相符。在接受肺炎、肺水肿和巨细胞病毒血症治疗后,患者在移植后2个月出院。肝移植后18个月,尽管他因真菌性肺炎接受治疗且由于肾替代治疗撤机不成功而正在考虑肾移植,但患者肝功能稳定,无移植物抗宿主病迹象,也无急性淋巴细胞白血病复发迹象。总之,尽管干细胞移植背景下的严重窦性阻塞综合征预后较差,但我们建议,对于造血干细胞移植后出现危及生命的肝功能障碍的特定患者,应考虑进行已故供体肝移植治疗。