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Clinicopathologic features of late-onset veno-occlusive disease/sinusoidal obstruction syndrome after high dose intravenous busulfan and hematopoietic cell transplant

机译:大剂量静脉注射白消安和造血细胞移植后迟发性静脉闭塞性疾病/窦性阻塞综合征的临床病理特征

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Most cases of veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) occur <21 days after allogeneic hematopoietic stem cell transplant (HCT). Rarely, however, VOD/SOS can occur later, and can be confused with other causes. We report the clinicopathologic features of eight patients with advanced hematologic malignancies developing VOD/SOS >30 days after dose-escalated busulfan/fludarabine/alemtuzumab and HCT. Median time to diagnosis was 52 days (range: 33-77). For seven patients, VOD/SOS was confirmed by liver biopsies showing classical features including reticulin deposition within sinusoids, central vein occlusions, hepatocyte atrophyecrosis, sinusoidal/perivenular hemorrhage and sparing of portal tracts. VOD/SOS risk was directly related to higher busulfan plasma exposures. Two patients died from VOD/SOS, and in another two patients VOD/SOS was contributory to death. Late-onset VOD/SOS may be underrecognized and should be considered in the differential diagnosis of patients undergoing HCT, particularly after high dose busulfan. Liver biopsy should be entertained even late in the course if appropriate signs/symptoms exist.
机译:静脉阻塞性疾病/正弦窦阻塞综合征(VOD / SOS)的大多数情况发生在同种异体造血干细胞移植(HCT)之后的21天之内。但是,很少会在以后发生VOD / SOS,并且可能与其他原因混淆。我们报告了八剂白消安/氟达拉滨/ alemtuzumab和HCT剂量升高后,发展为VOD / SOS> 30天的8例晚期血液系统恶性肿瘤的临床病理特征。诊断中位时间为52天(范围:33-77)。对于7例患者,通过肝活检证实了VOD / SOS,表现出经典特征,包括网状窦内网状蛋白沉积,中心静脉阻塞,肝细胞萎缩/坏死,正弦/周缘出血和门脉保留。 VOD / SOS风险与白消安血浆暴露量增加直接相关。两名患者死于VOD / SOS,另外两名患者死于VOD / SOS。迟发性VOD / SOS可能未被充分认识,在进行HCT的患者的鉴别诊断中应考虑考虑,特别是在大剂量白消安之后。如果存在适当的体征/症状,则应在病程后期进行肝活检。

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