Brown A P, Lane J C, Murayama S, Vollmer D G
Department of Neurosurgery, Washington University School of Medicine, St. Louis, Missouri.
J Neurosurg. 1990 Oct;73(4):623-7. doi: 10.3171/jns.1990.73.4.0623.
Whipple's disease is infrequently considered in the differential diagnosis of patients presenting with progressive neurological deterioration. This is in part a result of the relative rarity of this entity and in part due to the more frequent initial presentation of the disease with gastrointestinal, musculoskeletal, or cardiovascular symptoms. A case is described in which the neurological symptoms of progressive dementia and weakness were seen in the relative absence of non-neurological symptomatology. The diagnosis of Whipple's disease was made from a brain biopsy. The neuropathology of Whipple's disease of the central nervous system is described and the importance of considering it as a treatable entity in the differential diagnosis of progressive neurological deterioration, despite the absence of systemic symptomatology, is stressed.
在出现进行性神经功能恶化的患者鉴别诊断中,惠普尔病很少被考虑。这部分是由于该疾病相对罕见,部分是因为该疾病最初更常表现为胃肠道、肌肉骨骼或心血管症状。本文描述了一例病例,该病例在相对缺乏非神经症状的情况下出现了进行性痴呆和虚弱等神经症状。通过脑活检确诊为惠普尔病。描述了中枢神经系统惠普尔病的神经病理学,并强调了尽管没有全身症状,但在进行性神经功能恶化的鉴别诊断中,将其视为可治疗疾病的重要性。