Arumugam Praveen, Singh Lovelina, Agarwal Puneet, Shetti Suraj, Sharan Shalini
Internal Medicine, Max Smart Super Speciality Hospital, Saket, New Delhi, IND.
Neurology, Max Smart Super Speciality Hospital, Saket, New Delhi, IND.
Cureus. 2024 Jul 17;16(7):e64758. doi: 10.7759/cureus.64758. eCollection 2024 Jul.
Progressive multifocal leukoencephalopathy (PML) is considered an often fatal, demon-leading disease primarily associated with immunosuppression. Immunocompromised individuals predominantly exhibit this manifestation, while immunocompatible patients rarely encounter it. We present a unique case of PML in an immunocompetent individual who initially presented with stroke-like symptoms, received management, and was subsequently discharged. He returned to our hospital a few days later with similar complaints, prompting further investigations that revealed PML, a condition often overlooked, especially in individuals with an intact immune system. Although he received successful treatment with mefloquine and other anti-malarial medications and followed up on an outpatient basis, his subsequent outcome was unfavourable. As a result, this case emphasises the importance of having PML as a significant differential and therapeutic option.
进行性多灶性白质脑病(PML)被认为是一种通常致命的、恶魔般的疾病,主要与免疫抑制有关。免疫功能低下的个体主要表现出这种症状,而免疫功能正常的患者很少遇到这种情况。我们报告了一例免疫功能正常个体发生PML的独特病例,该个体最初表现为类似中风的症状,接受治疗后出院。几天后他因类似症状再次回到我院,促使进一步检查,结果发现了PML,这种情况常常被忽视,尤其是在免疫系统完好的个体中。尽管他接受了甲氟喹和其他抗疟药物的成功治疗并接受了门诊随访,但其后续结果并不理想。因此,该病例强调了将PML作为重要鉴别诊断和治疗选择的重要性。