{"title":"Extramedullary Relapse of Acute B-Lymphoblastic Leukemia Leading to Paraplegia in a Child with Down Syndrome.","authors":"Li Yang, Shi Luo, Ping Ye","doi":"10.7754/Clin.Lab.2024.241052","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Acute B-lymphoblastic leukemia (B-ALL) is a common malignancy in children. Patients with Trisomy 21 (Down syndrome) are at a higher risk of developing hematologic disorders. Despite advances in treatment, extramedullary relapse remains a challenge, particularly when it manifests as spinal cord compression leading to paraplegia, a rare but severe complication.</p><p><strong>Methods: </strong>We describe the clinical course of an 11-year-old male with Trisomy 21, diagnosed with B-ALL. The patient was treated with standard chemotherapy (VDLP regimen) followed by central nervous system prophylaxis through lumbar puncture and intrathecal chemotherapy. Despite achieving minimal residual disease (MRD)-negative status, the patient developed progressive lower back pain and acute paraplegia. Imaging studies and subsequent spinal surgery were performed to diagnose and manage the spinal cord lesion.</p><p><strong>Results: </strong>The patient's spinal pathology confirmed a relapse of B-ALL with extramedullary involvement. Immunohistochemistry of the tumor showed markers consistent with B-lymphoblastic leukemia/lymphoma. Chemotherapy-induced remission was initially achieved, but the patient experienced bone marrow suppression after each cycle, leading to further hospitalization and supportive treatments. Postsurgical findings showed no CNS involve-ment, and bone marrow MRD remained negative.</p><p><strong>Conclusions: </strong>This case highlights the complexity of managing B-ALL in children with Trisomy 21, who may be prone to extramedullary relapse despite systemic remission. Early recognition of spinal symptoms and prompt surgical intervention are critical in preventing irreversible neurological damage such as paraplegia. This case underscores the need for vigilant monitoring and tailored therapeutic strategies in high-risk populations.</p>","PeriodicalId":10384,"journal":{"name":"Clinical laboratory","volume":"71 4","pages":""},"PeriodicalIF":0.7000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical laboratory","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.7754/Clin.Lab.2024.241052","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Acute B-lymphoblastic leukemia (B-ALL) is a common malignancy in children. Patients with Trisomy 21 (Down syndrome) are at a higher risk of developing hematologic disorders. Despite advances in treatment, extramedullary relapse remains a challenge, particularly when it manifests as spinal cord compression leading to paraplegia, a rare but severe complication.
Methods: We describe the clinical course of an 11-year-old male with Trisomy 21, diagnosed with B-ALL. The patient was treated with standard chemotherapy (VDLP regimen) followed by central nervous system prophylaxis through lumbar puncture and intrathecal chemotherapy. Despite achieving minimal residual disease (MRD)-negative status, the patient developed progressive lower back pain and acute paraplegia. Imaging studies and subsequent spinal surgery were performed to diagnose and manage the spinal cord lesion.
Results: The patient's spinal pathology confirmed a relapse of B-ALL with extramedullary involvement. Immunohistochemistry of the tumor showed markers consistent with B-lymphoblastic leukemia/lymphoma. Chemotherapy-induced remission was initially achieved, but the patient experienced bone marrow suppression after each cycle, leading to further hospitalization and supportive treatments. Postsurgical findings showed no CNS involve-ment, and bone marrow MRD remained negative.
Conclusions: This case highlights the complexity of managing B-ALL in children with Trisomy 21, who may be prone to extramedullary relapse despite systemic remission. Early recognition of spinal symptoms and prompt surgical intervention are critical in preventing irreversible neurological damage such as paraplegia. This case underscores the need for vigilant monitoring and tailored therapeutic strategies in high-risk populations.
背景:急性b淋巴细胞白血病(Acute b lymphoblastic leukemia, B-ALL)是儿童常见的恶性肿瘤。患有21三体(唐氏综合症)的患者患血液系统疾病的风险更高。尽管治疗取得了进展,但髓外复发仍然是一个挑战,特别是当它表现为脊髓压迫导致截瘫时,这是一种罕见但严重的并发症。方法:我们描述了一个11岁的男性21三体,诊断为B-ALL的临床过程。患者接受标准化疗(VDLP方案),然后通过腰椎穿刺和鞘内化疗进行中枢神经系统预防。尽管达到了微小残留病(MRD)阴性状态,但患者出现了进行性腰痛和急性截瘫。影像学检查和随后的脊柱手术进行诊断和处理脊髓病变。结果:患者脊柱病理证实B-ALL复发伴髓外受累。肿瘤免疫组化显示与b淋巴细胞白血病/淋巴瘤一致的标志物。化疗诱导的缓解最初是实现的,但患者在每个周期后经历骨髓抑制,导致进一步住院和支持治疗。术后发现无中枢神经受累,骨髓MRD为阴性。结论:该病例突出了21三体儿童B-ALL治疗的复杂性,尽管全身缓解,但他们可能容易髓外复发。脊柱症状的早期识别和及时的手术干预对于预防不可逆的神经损伤(如截瘫)至关重要。该病例强调了对高危人群进行警惕监测和量身定制治疗策略的必要性。
期刊介绍:
Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.