慢性髓系白血病原细胞危象中孤立性中枢神经系统复发1例。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL Journal of Yeungnam medical science Pub Date : 2025-01-01 Epub Date: 2024-12-19 DOI:10.12701/jyms.2025.42.17
Hari Priya Raghvan, Caroline Ho Siew Ling, Wee Shiang Yui, Boo Yang Liang, Ehram Jamian, Indhira Subbiah
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引用次数: 0

摘要

慢性髓性白血病(CML)通常从慢性期发展到加速期,并最终发展为细胞危象,如果不及时治疗,通常会累及骨髓和外周血。中枢神经系统(CNS)受累是CML的一个不常见的表现,特别是作为孤立的中枢神经系统复发。在此,我们报告一例罕见的CML淋巴细胞危象伴孤立的中枢神经系统复发。46岁女性,淋巴细胞危象伴有CML,既往接受化疗和酪氨酸激酶抑制剂治疗,现表现为视觉障碍。影像学和脑脊液分析证实白血病浸润中枢神经系统,无系统性疾病的证据。孤立性中枢神经系统受累是CML的非典型并发症,由于血脑屏障限制了全身治疗的疗效,因此给治疗带来了重大挑战。随后,患者接受了针对中枢神经系统的鞘内化疗。尽管积极治疗,由于标准疗法对中枢神经系统的渗透有限,中枢神经系统复发仍然是一个主要问题。该病例强调了早期识别CML患者(特别是那些有原细胞危象的患者)中枢神经系统症状的重要性,并强调了定制治疗策略来管理这种罕见且具有挑战性的表现的必要性。
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Isolated central nervous system relapse in blast crisis of chronic myeloid leukemia: a case report.

Chronic myeloid leukemia (CML) typically progresses from a chronic phase to an accelerated phase, and eventually to a blast crisis, often involving the bone marrow and peripheral blood, if left untreated. Central nervous system (CNS) involvement is an uncommon manifestation of CML, particularly as an isolated CNS relapse. Here, we present a rare case of CML in lymphoid blast crisis with an isolated CNS relapse. A 46-year-old female with underlying CML in lymphoid blast crisis, previously treated with chemotherapy and tyrosine kinase inhibitors, presented with visual disturbances. Imaging and cerebrospinal fluid analysis confirmed leukemic infiltration of the CNS without evidence of a systemic disease. Isolated CNS involvement is an atypical complication of CML and presents significant therapeutic challenges owing to the blood-brain barrier, which limits the efficacy of systemic therapies. Subsequently, the patient was treated with intrathecal chemotherapy targeting the CNS. Despite aggressive treatment, CNS relapse remains a major concern due to the limited penetration of standard therapies into the CNS. This case underscores the importance of early recognition of CNS symptoms in CML patients, particularly in those with blast crisis, and highlights the need for tailored therapeutic strategies to manage this rare and challenging manifestation.

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