复发性急性淋巴细胞白血病患者颅底肿瘤的精细化治疗

IF 0.6 Q4 CLINICAL NEUROLOGY Journal of Neurological Surgery Reports Pub Date : 2024-04-01 DOI:10.1055/a-2297-4265
Geena Jung, Emery Buckner-Wolfson, Adit Tal, Ryan Fatemi, Timothy Kim, Genesis Liriano, Andrew Kobets
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摘要

导言:涉及中枢神经系统(CNS)的急性淋巴细胞白血病复发是一个重要问题,会导致发病率和死亡率。鉴于中枢神经系统复发患者的预后较差,了解涉及颅内复发的急性淋巴细胞白血病如何表现和治疗至关重要。在此,我们介绍一例复杂的儿童 ALL 复发病例:病例报告:一名 11 岁的患者因广泛颅底病变和脑外膜病变导致 ALL 双重复发。对于颅底病变,她接受了化疗和放疗等非手术治疗,病变面积明显缩小。然而,在完成治疗五个月后,她被发现早期复发并伴有脑室外膜增厚,导致脑积水。医生成功地为她植入了分流器。目前,她每月接受一次鞘内化疗,每两个月进行一次脑脊液采样和骨髓活检:讨论:我们报告了化疗和放疗对缩小广泛颅底病灶的效果,使患者免于手术风险。该患者初次复发时颅底病灶较大且累及颅内,这在复发的 ALL 中并不多见。另外,早期复发的脑膜疾病也使该病例更加独特,治疗方法也更加微妙。在此,我们展示了成功治疗患者的多学科方法,这有助于指导今后类似患者的治疗。
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Nuanced Management of a Skull Base Tumor in the Setting of Relapsed Acute Lymphoblastic Leukemia
Introduction: Relapsed acute lymphoblastic leukemia involving the central nervous system (CNS) is a significant issue that contributes to both morbidity and mortality. Given the poor outcomes in patients with CNS relapse, understanding how ALL involving intracranial relapse presents and is treated is critical. Here, we present a complex case of relapsed recurrent ALL in a pediatric patient. Case Report: An eleven-year-old patient presented with double relapse of ALL in the form of an extensive skull base lesion and again with leptomeningeal disease. For the skull base lesion, she was treated non-surgically with chemotherapy and radiation, which led to a remarkable reduction in the size of the lesion. However, she was found to have early recurrence with leptomeningeal enhancement resulting in hydrocephalus five months after completing therapy. A shunt was placed successfully. Currently, she is being managed with monthly intrathecal chemotherapy with CSF sampling and bone marrow biopsies every two months. Discussion: We report the significant effect of chemotherapy and radiotherapy in reducing the size of the extensive skull base lesion, saving the patient from the risks associated with surgery. This patient’s initial relapse, with a large skull base lesion that had intracranial involvement, is an unusual presentation of relapsed ALL. The additional early recurrence of leptomeningeal disease further makes this case unique and the management even more nuanced. Here, we demonstrate a multidisciplinary approach for the successful treatment of our patient, which can help guide the management of similar patients in the future.
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