Li Zhihui, Wen Xiaopei, Geng Yanping, Wu Tong
Department of Bone Marrow Transplantation, Beijing Boren Hospital, Beijing, China.
J Pediatr Hematol Oncol. 2021 Nov 1;43(8):e1088-e1092. doi: 10.1097/MPH.0000000000002044.
The common etiology of central nervous system (CNS) complications after allogeneic hematopoietic stem cell transplantation (allo-HSCT) includes CNS infection, metabolic abnormalities, drug toxicity, cerebrovascular events, Epstein-Barr virus-associated posttransplant lymphoproliferative diseases, and hematologic CNS relapse of leukemia. Although graft-versus-host disease (GVHD) is a major complication of allo-HSCT, its CNS involvement is exceedingly rare.
In this report, we describe a patient who exhibited acute myeloid leukemia with t(8;21) (q22;q22) and who suddenly lost visual acuity ~1 year after receipt of allo-HSCT. Given the observation of negative cerebrospinal fluid findings, cyclosporine-related encephalopathy, intracranial hemorrhage, CNS infection, leukemia recurrence, and tumors were excluded. He was diagnosed with both CNS and pulmonary GVHD. After steroid treatment, the lesions gradually reduced in images acquired via cranial and pulmonary computed tomography.
CNS-GVHD is a rare, serious complication of allo-HSCT that is difficult to diagnose. Biopsy and autopsy may identify the CNS as the target of GVHD in some patients. Treatment is mainly based on the use of immunosuppressive drugs, including high doses of steroids. Early diagnosis and treatment can improve disease outcome.
异基因造血干细胞移植(allo-HSCT)后中枢神经系统(CNS)并发症的常见病因包括CNS感染、代谢异常、药物毒性、脑血管事件、爱泼斯坦-巴尔病毒相关的移植后淋巴细胞增生性疾病以及白血病的血液学CNS复发。尽管移植物抗宿主病(GVHD)是allo-HSCT的主要并发症,但其累及CNS极为罕见。
在本报告中,我们描述了一名患有t(8;21) (q22;q22)急性髓系白血病的患者,其在接受allo-HSCT约1年后突然视力丧失。鉴于脑脊液检查结果为阴性,排除了环孢素相关脑病、颅内出血、CNS感染、白血病复发和肿瘤。他被诊断为CNS和肺部GVHD。经类固醇治疗后,通过头颅和肺部计算机断层扫描获得的图像中病变逐渐减轻。
CNS-GVHD是allo-HSCT罕见且严重的并发症,难以诊断。活检和尸检可能会在一些患者中确定CNS为GVHD的靶器官。治疗主要基于使用免疫抑制药物,包括高剂量类固醇。早期诊断和治疗可改善疾病预后。