Beşişik Sevgi Kalayoğlu, Oztürk Gülistan Bahat, Calişkan Yaşar, Sargin Deniz
Department of Internal Medicine, Division of Hematology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Turk J Gastroenterol. 2005 Mar;16(1):34-7.
Transplantation-associated thrombotic microangiopathy has been associated with significantly reduced survival following allogeneic bone marrow transplantation. We describe here the course of Transplantation-associated thrombotic microangiopathy and hepatic veno-occlusive disease, and response to plasma exchange therapy. A 19-year-old male patient underwent hematopoietic stem cell transplantation (HSCT) from his HLA-matched brother for lymphoblastic lymphoma in the first complete remission. Transplantation-associated thrombotic microangiopathy was diagnosed 17 days after transplantation. At that time, neurological abnormalities were not present. Cyclosporin A (CsA) was discontinued. Hematological stabilization was recorded. On day +20, abdominal distention, painful hepatomegaly and ascites complicated the clinical picture. With a high hepatic venous pressure gradient (18mmH20), veno-occlusive disease of the liver was diagnosed and defibrotide was started, which resulted in a dramatic cessation of pain and increase in urinary output. However, transplantation-associated thrombotic microangiopathy-related symptoms progressed and plasma exchange was instituted, which resulted in worsening of veno-occlusive disease symptoms. He was referred to the Intensive Care Unit due to respiratory compromise and was intubated. Plasma exchange was continued in order after hemofiltration. In three days, fever resolved, hemofiltration could be stopped, and ventilator dependence ended. After 19 aphereses, serum LDH level returned to normal and schistocytes were minimal on microscopic examination of the blood film. Platelet count increase was more gradual. Plasma exchange was discontinued. On the 40th day of defibrotide, all symptoms related with veno-occlusive disease were resolved and defibrotide was stopped. We think that our case is important to establish the relation and management strategy of these two small vessel complications of HSCT.
移植相关血栓性微血管病与异基因骨髓移植后生存率显著降低相关。我们在此描述移植相关血栓性微血管病和肝静脉闭塞病的病程以及对血浆置换治疗的反应。一名19岁男性患者因处于首次完全缓解期的淋巴细胞性淋巴瘤,接受了来自其HLA匹配同胞兄弟的造血干细胞移植(HSCT)。移植后17天诊断为移植相关血栓性微血管病。当时尚无神经学异常。停用环孢素A(CsA)。血液学情况稳定。在+20天时,腹胀、肝肿大伴疼痛和腹水使临床情况复杂化。肝静脉压力梯度较高(18mmH2O),诊断为肝静脉闭塞病并开始使用去纤苷,这导致疼痛戏剧性缓解且尿量增加。然而,移植相关血栓性微血管病相关症状仍进展,于是进行血浆置换,但这导致肝静脉闭塞病症状恶化。由于呼吸功能不全,他被转入重症监护病房并插管。在血液滤过之后继续进行血浆置换。三天内,发热消退,血液滤过可以停止,呼吸机依赖解除。经过19次单采血浆术,血清乳酸脱氢酶水平恢复正常,血涂片显微镜检查显示破碎红细胞极少。血小板计数增加较为缓慢。停止血浆置换。在使用去纤苷第40天时,所有与肝静脉闭塞病相关的症状均已缓解,停用去纤苷。我们认为我们的病例对于确立HSCT这两种小血管并发症的关系及管理策略具有重要意义。