Trivedi Jaya R, Wolfe Gil I, Nations Sharon P, Burns Dennis K, Bryan Wilson W, Dewey Richard B
Department of Neurology, University of Texas Southwestern Medical Center, Dallas, 75390, USA.
Arch Neurol. 2003 May;60(5):764-6. doi: 10.1001/archneur.60.5.764.
Adult polyglucosan body disease (PGBD) is rare and typically presents with upper and lower motor neuron involvement and neurogenic bladder. Extrapyramidal features are unusual in PGBD and are presumed secondary to widespread pathology that includes the basal ganglia. There are no prior reports of Lewy bodies in PGBD.
To report a unique finding of Lewy bodies in a patient with PGBD. REPORT OF A CASE A 46-year-old woman initially presented with a 4-year history of resting tremor. The tremor responded to levodopa therapy. Several months later, she developed upper and lower motor neuron involvement and other clinical features of PGBD. A sural nerve biopsy specimen revealed intra-axonal polyglucosan bodies that confirmed the clinical diagnosis. Bulbar and limb weakness progressed, and she developed dementia. She died 6 years after onset. At autopsy, extensive polyglucosan body formation was found in many regions of the central nervous system. In addition, numerous alpha-synuclein staining Lewy bodies were observed in the substantia nigra, accompanied by marked neuron depopulation.
To our knowledge, this is the first report of adult PGBD associated with Lewy bodies and levodopa-responsive tremor. Although polyglucosan bodies were seen in substantia nigra, it is most likely that our patient had coexisting Parkinson disease.
成人多聚葡萄糖体病(PGBD)罕见,通常表现为上下运动神经元受累及神经源性膀胱。锥体外系特征在PGBD中不常见,推测是继发于包括基底神经节在内的广泛病变。此前尚无PGBD中存在路易小体的报道。
报告1例PGBD患者中发现路易小体这一独特发现。
一名46岁女性最初表现为有4年静止性震颤病史。震颤对左旋多巴治疗有反应。数月后,她出现上下运动神经元受累及PGBD的其他临床特征。腓肠神经活检标本显示轴突内多聚葡萄糖体,证实了临床诊断。延髓和肢体无力进展,她出现痴呆。发病6年后死亡。尸检发现中枢神经系统许多区域有广泛的多聚葡萄糖体形成。此外,在黑质中观察到大量α-突触核蛋白染色的路易小体,伴有明显的神经元减少。
据我们所知,这是首例与路易小体和左旋多巴反应性震颤相关的成人PGBD报告。尽管在黑质中发现了多聚葡萄糖体,但我们的患者很可能同时患有帕金森病。