Roth Heidi L, Eskin Thomas A, Kendall Diane L, Heilman Kenneth M
Department of Neurology, University of North Carolina, Chapel Hill, North Carolina, USA.
Neurocase. 2006 Aug;12(4):221-7. doi: 10.1080/13554790600837347.
A loss of speech can be related to disorders of the motor units (paresis), language deficits (aphasia), or speech programming deficits (apraxia of speech). Although apraxia of speech has been reported to be associated with degenerative diseases, we observed a patient with a unique constellation of signs that included apraxia of speech, oculo-orofacial apraxia and a supranuclear ophthalmoplegia in the absence of extrapyramidal (Parkinsonian) signs. Post-mortem examination revealed a loss of neurons in the frontal and temporal regions, but there was also a marked loss of neurons and astrogliosis in the caudate, claustrum, globus pallidus, substantia nigra, and loss of axons in the anterior cerebral peduncles. This patient's clinical presentation and the pathological correlates suggest that he might have suffered with a distinct disorder we call progressive oculo-orofacial-speech apraxia or POOSA.
言语丧失可能与运动单位障碍(轻瘫)、语言缺陷(失语症)或言语编程缺陷(言语失用症)有关。尽管据报道言语失用症与退行性疾病有关,但我们观察到一名患者具有独特的体征组合,包括言语失用症、眼口面部失用症和核上性眼肌麻痹,且无锥体外系(帕金森氏症)体征。尸检显示额叶和颞叶区域的神经元丢失,但尾状核、屏状核、苍白球、黑质也有明显的神经元丢失和星形胶质细胞增生,大脑脚前部的轴突也有丢失。该患者的临床表现和病理相关性表明,他可能患有一种我们称为进行性眼口面部言语失用症(POOSA)的独特疾病。