Department of Pathology, Dalhousie University, 715 - 5788 University Avenue, Halifax, NS, B3H 2Y9, Canada.
Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, 1468 Madison Ave, New York, NY, 10029, USA.
Hum Pathol. 2023 Nov;141:170-182. doi: 10.1016/j.humpath.2023.07.007. Epub 2023 Aug 2.
Graft-versus-host disease (GVHD) is one of the serious complications that may develop after hematopoietic cell transplantation (HCT), for hematologic malignancies, solid organ transplantation, and other hematologic disorders. GVHD develops due to T lymphocytes present in the graft attacking the host antigens, which results in tissue damage. A significant number of HCT patients develop acute or chronic GVHD, which may affect multiple organs including the liver. The diagnosis of hepatic GVHD (hGVHD) is challenging as many other conditions in HCT patients may lead to liver dysfunction. Particularly challenging among the various conditions that give rise to liver dysfunction is differentiating sinusoidal obstruction syndrome and drug-induced liver injury (DILI) from hGVHD on clinical grounds and laboratory tests. Despite the minimal risks involved in performing a liver biopsy, the information gleaned from the histopathologic changes may help in the management of these very complex patients. There is a spectrum of histologic features found in hGVHD, and most involve histopathologic changes affecting the interlobular bile ducts. These include nuclear and cytoplasmic abnormalities including dysmorphic bile ducts, apoptosis, and cholangiocyte necrosis, among others. The hepatitic form of hGVHD typically shows severe acute hepatitis. With chronic hGVHD, there is progressive bile duct loss and eventually fibrosis. Accurate diagnosis of hGVHD is paramount so that timely treatment and management can be initiated. Techniques to prevent and lower the risk of GVHD from developing have recently evolved. If a diagnosis of acute GVHD is made, the first-line of treatment is steroids. Recurrence is common and steroid resistance or dependency is not unusual in this setting. Second-line therapies differ among institutions and have not been uniformly established. The development of GVHD, particularly hGVHD, is associated with increased morbidity and mortality.
移植物抗宿主病(GVHD)是造血细胞移植(HCT)后可能发生的严重并发症之一,可发生于血液系统恶性肿瘤、实体器官移植和其他血液系统疾病。GVHD 是由于移植物中的 T 淋巴细胞攻击宿主抗原而引起的组织损伤。相当数量的 HCT 患者会发生急性或慢性 GVHD,可能会影响包括肝脏在内的多个器官。肝 GVHD(hGVHD)的诊断具有挑战性,因为 HCT 患者的许多其他情况可能导致肝功能障碍。在导致肝功能障碍的各种情况下,特别具有挑战性的是,根据临床和实验室检查结果,从 hGVHD 中区分出窦状隙阻塞综合征和药物性肝损伤(DILI)。尽管进行肝活检的风险很小,但从组织病理学变化中获得的信息可能有助于管理这些非常复杂的患者。hGVHD 存在一系列组织学特征,大多数涉及影响小叶间胆管的组织病理学变化。这些变化包括核和细胞质异常,包括畸形胆管、细胞凋亡和胆管细胞坏死等。hGVHD 的肝炎型通常表现为严重的急性肝炎。慢性 hGVHD 存在进行性胆管丢失,最终导致纤维化。准确诊断 hGVHD 至关重要,以便及时开始治疗和管理。预防和降低 GVHD 发展风险的技术最近已经有所发展。如果诊断为急性 GVHD,一线治疗是类固醇。在此情况下,复发很常见,类固醇耐药或依赖并不罕见。二线治疗在不同机构之间有所不同,尚未得到统一确立。GVHD 的发展,特别是 hGVHD 的发展,与发病率和死亡率的增加相关。