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中枢神经系统的惠普尔病。

Whipple's disease of the central nervous system.

作者信息

Silbert S W, Parker E, Horenstein S

出版信息

Acta Neuropathol. 1976 Sep 15;36(1):31-8. doi: 10.1007/BF00685145.

Abstract

Whipple's disease presenting as a neurological disease without gastrointestinal symptoms is an unusual occurrence. A 40 year old man suffered hypersomnia, memory loss and progressive ophthalmoplegia for 6 months prior to death. The nature of this disease was not established during life. Extensive granulomatous inflammation affecting the hypothalamus, hippocampus and periaqueductal gray matter of the brain was found to represent Whipple's disease by electron microscopy. Characteristic lesions were also present in spleen, mesenteric lymph nodes, small intestine and myocardium. Bacillary bodies and membranous inclusions similar to those seen in visceral lesions of Whipple's disease were present in macrophages. The findings supported the theory of direct involvement of the central nervous system by bacilli rather than a metabolic origin for the lesions.

摘要

以神经疾病形式出现且无胃肠道症状的惠普尔病是一种罕见情况。一名40岁男性在死前6个月出现嗜睡、记忆力减退和进行性眼肌麻痹。该疾病的性质在生前未明确。通过电子显微镜检查发现,广泛的肉芽肿性炎症累及下丘脑、海马体和脑导水管周围灰质,提示为惠普尔病。脾脏、肠系膜淋巴结、小肠和心肌也存在特征性病变。巨噬细胞中可见与惠普尔病内脏病变中所见相似的杆菌体和膜状包涵体。这些发现支持了杆菌直接累及中枢神经系统而非病变代谢起源的理论。

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