Newby Rachel E, Thorpe Deborah E, Kempster Peter A, Alty Jane E
Neurosciences Department Monash Medical Centre Melbourne Victoria Australia.
Department of Neurology Leeds General Infirmary Leeds United Kingdom.
Mov Disord Clin Pract. 2017 Jul-Aug;4(4):478-485. doi: 10.1002/mdc3.12493. Epub 2017 May 22.
Before 1911, when Hermann Oppenheim introduced the term dystonia, this movement disorder lacked a unifying descriptor. While words like epilepsy, apoplexy, and palsy have had their meanings since antiquity, references to dystonia are much harder to identify in historical documents. Torticollis is an exception, although there is difficulty distinguishing dystonic torticollis from congenital muscular torticollis. There are, nevertheless, possible representations of dystonia in literature and visual art from the pre-modern world. Eighteenth century systematic nosologists such as Linnaeus, de Sauvages, and Cullen had attempted to classify some spasmodic conditions, including torticollis. But only after Charcot's contributions to clinical neuroscience were the various forms of generalized and focal dystonia clearly delineated. They were categorized as : Charcot's term for conditions without an identifiable neuroanatomical cause. For a time thereafter, psychoanalytic models of dystonia based on Freud's ideas about unconscious conflicts transduced into physical symptoms were ascendant, although there was always a dissenting "organic" school. With the rise of subspecialization in movement disorders during the 1970s, the pendulum swung strongly back toward organic causation. David Marsden's clinical and electrophysiological research on the adult-onset focal dystonias was particularly important in establishing a physical basis for these disorders. We are still in a period of "living history" of dystonia, with much yet to be understood about pathophysiology. Rigidly dualistic models have crumbled in the face of evidence of electrophysiological and psychopathological overlap between organic and functional dystonia. More flexible biopsychosocial frameworks may address the demand for new diagnostic and therapeutic rationales.
1911年之前,当赫尔曼·奥本海姆引入“肌张力障碍”一词时,这种运动障碍缺乏一个统一的描述词。虽然癫痫、中风和麻痹等词自古就有其含义,但在历史文献中很难找到关于肌张力障碍的记载。斜颈是个例外,不过区分肌张力障碍性斜颈和先天性肌性斜颈存在困难。然而,在前现代世界的文学和视觉艺术中可能存在肌张力障碍的表现。18世纪的系统疾病分类学家,如林奈、德·索瓦热和卡伦,曾试图对一些痉挛性疾病进行分类,包括斜颈。但直到夏科对临床神经科学做出贡献之后,各种形式的全身性和局灶性肌张力障碍才得以明确界定。它们被归类为:夏科用来描述无明确神经解剖学病因的病症的术语。此后一段时间,基于弗洛伊德关于无意识冲突转化为身体症状的观点的肌张力障碍精神分析模型占了上风,尽管一直存在持异议的“器质性”学派。随着20世纪70年代运动障碍亚专业的兴起,钟摆又强烈地摆回了器质性病因的方向。大卫·马斯登对成人起病的局灶性肌张力障碍的临床和电生理研究,在为这些疾病确立物理基础方面尤为重要。我们仍处于肌张力障碍的“活历史”时期,其病理生理学仍有许多有待了解之处。面对器质性和功能性肌张力障碍之间电生理和精神病理学重叠的证据,僵化的二元模型已经瓦解。更灵活的生物心理社会框架可能满足对新的诊断和治疗原理的需求。