Suzuki Makiko, Kawasaki Hideya, Masaki Katsuhisa, Suzuki Satoshi O, Terada Tatsuhiro, Tsuchida Takashi, Tokuyama Tsutomu, Kono Satoshi, Komori Takashi, Baba Satoshi, Kira Jun-ichi, Miyajima Hiroaki
The First Department of Medicine, Department of Neurology, Hamamatsu University School of Medicine, Japan.
Intern Med. 2013;52(16):1825-32. doi: 10.2169/internalmedicine.52.0425. Epub 2012 Mar 1.
We herein report an autopsy case of the Marburg variant of multiple sclerosis (MS). A 29-year-old woman developed acute and progressive neurological symptoms. A diagnosis of MS was suspected based on the patient's clinical background and brain MRI findings and the lack of evidence of malignancy on a brain biopsy. Despite the administration of typical treatment for MS, a fatal outcome occurred three months after disease onset. The autopsy revealed multiple inflammatory demyelinating lesions in the central nervous system. In addition, two noteworthy histopathological features were observed compared with prototypical MS. We evaluate the pathogenic differences between the Marburg type and prototypical MS by discussing the neuropathology and cerebrospinal fluid (CSF) findings of our case.
我们在此报告一例马尔堡型多发性硬化症(MS)的尸检病例。一名29岁女性出现急性进行性神经症状。基于患者的临床背景、脑部MRI表现以及脑活检未发现恶性肿瘤证据,怀疑为MS。尽管给予了MS的典型治疗,但发病三个月后仍出现致命结局。尸检显示中枢神经系统存在多个炎性脱髓鞘病变。此外,与典型MS相比,观察到两个值得注意的组织病理学特征。我们通过讨论本病例的神经病理学和脑脊液(CSF)检查结果,评估马尔堡型与典型MS之间的致病差异。