Parker J C, Dyer M L, Paulsen W A
Department of Medical Biology, University of Tennessee Memorial Research Center, Knoxville.
J Clin Neuroophthalmol. 1987 Dec;7(4):244-9.
Neuronal intranuclear hyaline inclusion disease (NIHID) has been recognized in 14 patients. It usually occurs in the first and second decades but has been seen in the sixth. Both sexes are affected by this sporadic multisystem degenerative disorder that has involved the central and peripheral nervous systems with fibrillar and granular intranuclear inclusions. NIHID appears to be several variants of a multisystem degenerative disease as illustrated by the combination of a spontaneous, degenerative central and peripheral nervous system disorder with neuronal intranuclear inclusions and severe atherosclerotic coronary artery disease in a 23-year-old white man. Beginning at 11 years of age, this patient had experienced diffuse muscle spasms, dysarthria, dysphagia, tremors, ataxia, oculogyric crises, progressive muscle weakness, and atrophy. At autopsy, neuronal intranuclear hyaline inclusions and neuronal loss were seen in his brain, brainstem, cerebellum, spinal cord, bowel, bladder, and esophagus. These fibrillary and granular Cowdry type A and B intraneuronal inclusions were consistent with the diagnosis of NIHID associated with severe coronary atherosclerosis.
神经元核内透明包涵体病(NIHID)已在14例患者中得到确认。它通常发生在第一个和第二个十年,但也有在第六个十年出现的情况。男女两性均可受这种散发性多系统退行性疾病影响,该疾病累及中枢和周围神经系统,并伴有核内纤维状和颗粒状包涵体。NIHID似乎是一种多系统退行性疾病的几种变体,如一名23岁白人男性中出现的自发性、退行性中枢和周围神经系统疾病合并神经元核内包涵体以及严重的动脉粥样硬化性冠状动脉疾病所表明的那样。该患者从11岁开始出现弥漫性肌肉痉挛、构音障碍、吞咽困难、震颤、共济失调、动眼危象、进行性肌肉无力和萎缩。尸检时,在其大脑、脑干、小脑、脊髓、肠道、膀胱和食管中发现了神经元核内透明包涵体和神经元丢失。这些纤维状和颗粒状的考德里A型和B型神经元内包涵体与伴有严重冠状动脉粥样硬化的NIHID诊断相符。