Knight Kathryn, Chien Siobhan, Koutsavlis Ioannis, Campbell Victoria
Core Medical Trainee, NHS Fife, Kirkaldy, UK.
Foundation Year Doctor, NHS Fife, Kirkaldy, UK.
BMJ Case Rep. 2020 Mar 22;13(3):e233552. doi: 10.1136/bcr-2019-233552.
A 59-year-old man, with a background of multiply relapsed myeloma, presented with a 3-week history of confusion, short-term memory impairment and behavioural changes. CT head showed bilateral white matter changes and numerous, large lytic lesions of the skull vault. MRI brain revealed multiple areas of hyperintensity on T2-weighted sequences which did not enhance (many of which showed diffusion restriction) unexpectedly bringing progressive multifocal leukoencephalopathy (PML) into the differential. Initial cerebrospinal fluid studies were largely unremarkable, aside from a mildly elevated protein; cultures were negative. PCR for the John Cunningham (JC) virus was positive. Considering the patient's medical history and rapidily progressive symptoms, a palliative approach was adopted, with the patient dying 14 days later. We present this case as an example of PML in a patient with multiple myeloma, highlighting the need to consider this diagnosis in an enlarging population of heavily treated, severely immunocompromised, patients.
一名59岁男性,有多次复发骨髓瘤病史,出现了3周的意识模糊、短期记忆障碍和行为改变。头颅CT显示双侧白质改变以及颅骨穹窿部多发、大片溶骨性病变。脑部MRI在T2加权序列上显示多个高信号区域,这些区域未强化(其中许多显示弥散受限),意外地使进行性多灶性白质脑病(PML)进入鉴别诊断范围。最初的脑脊液检查除蛋白轻度升高外,基本无异常;培养结果为阴性。约翰·坎宁安(JC)病毒的PCR检测呈阳性。考虑到患者的病史和快速进展的症状,采取了姑息治疗方法,患者于14天后死亡。我们将此病例作为多发性骨髓瘤患者发生PML的一个例子进行展示,强调在越来越多接受大量治疗、严重免疫受损的患者中需要考虑这一诊断。