Aamodt Whitley W, Siegler James E, Viaene Angela N, Rubenstein Michael N
Department of Neurology, Hospital of the University of Pennsylvania, 3W Gates Building, 3400 Spruce Street, Philadelphia, PA 19104, USA.
Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104, USA.
J Clin Neurosci. 2017 Sep;43:132-134. doi: 10.1016/j.jocn.2017.04.030. Epub 2017 May 16.
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease resulting from infection of oligodendrocytes in the central nervous system with John Cunningham virus. Although PML is commonly diagnosed in immunocompromised patients with human immunodeficiency virus, it can also arise in other immunodeficient states. In this report, we present an unusual case of PML occurring 40years after chemoradiation therapy for Hodgkin lymphoma in a patient with normal total lymphocyte counts on annual surveillance. Although current guidelines recommend annual complete blood counts for patients in remission, this testing may be insufficient to monitor patients with chronic CD4+ lymphopenia.
进行性多灶性白质脑病(PML)是一种脱髓鞘疾病,由中枢神经系统少突胶质细胞感染约翰·坎宁安病毒所致。尽管PML常见于感染人类免疫缺陷病毒的免疫功能低下患者,但也可发生于其他免疫缺陷状态。在本报告中,我们介绍了一例不寻常的PML病例,该病例发生在一名接受霍奇金淋巴瘤放化疗40年后的患者身上,该患者年度监测时总淋巴细胞计数正常。尽管目前的指南建议对缓解期患者进行年度全血细胞计数检查,但这种检测可能不足以监测慢性CD4+淋巴细胞减少的患者。