Halperin J J, Landis D M, Kleinman G M
Neurology. 1982 Jun;32(6):612-7. doi: 10.1212/wnl.32.6.612.
A 58-year-old man with dizziness and unsteady gait had a 10-year history of behavioral change, impotence, and a progressive peripheral neuropathy. CT revealed low-density, contrast-enhancing lesions in the right pontine tegmentum and the right medial temporal lobe. Temporal lobe biopsy contained a collection of mature histiocytes, with PAS-positive rod-shaped inclusions. These inclusions, when studied by electronmicroscopy, were seen to be membrane-bound bacilliform bodies. Peroral jejunal biopsy contained no such inclusions. Despite treatment with antibiotics, the patient's neurologic illness progressed, and he succumbed to intercurrent sepsis. We believe this to be the first instance in which a lesion of Whipple disease has been identified within the CNS by CT scan, and the diagnosis made antemortem, in the absence of demonstrable systemic disease.
一名58岁男性,有头晕和步态不稳症状,有10年行为改变、阳痿及进行性周围神经病变病史。CT显示右桥脑被盖部和右颞叶内侧有低密度、强化病变。颞叶活检发现一群成熟组织细胞,有PAS阳性棒状包涵体。经电子显微镜研究,这些包涵体为膜包被的杆状体。经口空肠活检未发现此类包涵体。尽管使用抗生素治疗,患者神经疾病仍进展,最终死于并发的败血症。我们认为这是首例通过CT扫描在中枢神经系统内发现惠普尔病病变且在生前作出诊断,而无明显全身性疾病表现的病例。