Collins S J, Ahlskog J E, Parisi J E, Maraganore D M
Department of Neurology, Mayo Clinic, Rochester, MN 55905.
J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):167-73. doi: 10.1136/jnnp.58.2.167.
All cases examined postmortem at the Mayo Clinic that met the classic neuropathological criteria for progressive supranuclear palsy (PSP) were identified for retrospective clinical analyses. The necropsy material was re-examined by a second neuropathologist to confirm the pathological diagnosis of PSP, yielding 12 cases. A range of clinical signs were documented in these patients, with numerous findings beyond those noted in the original descriptions of this disorder. Atypical clinical findings included absence of supranuclear gaze palsy (two cases), prominent asymmetry (two), arm dystonia (two), upper limb apraxia (two), myoclonus (two), chorea (one), eyelid opening apraxia (one), and respiratory disturbance (one). A definite clinical diagnosis of PSP had been made during life in only eight of the 12 patients. From the retrospective analysis of these 12 cases, a set of clinical criteria were developed for the premortem diagnosis of PSP emphasising differences from other akinetic-rigid disorders.
对梅奥诊所所有经尸检且符合进行性核上性麻痹(PSP)经典神经病理学标准的病例进行识别,以进行回顾性临床分析。尸检材料由另一位神经病理学家重新检查,以确认PSP的病理诊断,最终得到12例病例。记录了这些患者的一系列临床体征,发现了许多超出该疾病最初描述的表现。非典型临床发现包括无核上性凝视麻痹(2例)、明显不对称(2例)、手臂肌张力障碍(2例)、上肢失用症(2例)、肌阵挛(2例)、舞蹈症(1例)、眼睑开合失用症(1例)和呼吸障碍(1例)。12例患者中仅有8例在生前得到了明确的PSP临床诊断。通过对这12例病例的回顾性分析,制定了一套用于生前诊断PSP的临床标准,强调了与其他运动不能-强直型疾病的差异。