Ozer Suzan, Ozcan Halil, Dinç Gülser Senses, Ertuğrul Aygün, Rezaki Murat, Uluşahin Aylin
Hacettepe U Tip Fak., Psikiyatri AD, Cocuk Ruh Sağliği, Ankara.
Turk Psikiyatri Derg. 2009 Winter;20(4):392-7.
Modern psychiatric diagnostic systems classify neurological symptoms that cannot be explained by a physical disease or another psychiatric disorder as conversion disorder (CD) or dissociative motor disorder. It is a well-known fact that the overall rate of misdiagnosis of conversion symptoms is high. The most common presenting symptoms of misdiagnosed patients are gait and movement disturbances. Stiff-person syndrome (SPS) is a rare progressive autoimmune neurological disorder. The identification of antibodies against glutamic acid decarboxylase (GAD) in association with SPS provided an important contribution to the understanding of the pathophysiology of this syndrome. Patients may present with severe muscle rigidity and sudden contractions. Simultaneous contraction of agonist and antagonist muscles produces gait disturbance. SPS can be exacerbated by emotional stressors, and sudden auditory, visual, and tactile stimuli. Herein we present 2 patients that were referred for psychiatric assessment, because their neurological symptoms initially could not be explained by a neurological disease, and subsequently diagnosed as SPS. The aim of this case report is to draw attention to the psychiatric presentations of SPS and to emphasize the importance of complete psychiatric and neurological examination, including brain imaging and electrophysiological studies, in the differential diagnosis of CD.
现代精神科诊断系统将无法用躯体疾病或其他精神障碍解释的神经症状归类为转换障碍(CD)或分离性运动障碍。转换症状的总体误诊率很高,这是一个众所周知的事实。误诊患者最常见的症状表现是步态和运动障碍。僵人综合征(SPS)是一种罕见的进行性自身免疫性神经疾病。与SPS相关的谷氨酸脱羧酶(GAD)抗体的鉴定为理解该综合征的病理生理学做出了重要贡献。患者可能会出现严重的肌肉僵硬和突然收缩。主动肌和拮抗肌同时收缩会导致步态障碍。情绪应激源以及突然的听觉、视觉和触觉刺激会加重SPS。在此,我们报告2例因神经症状最初无法用神经疾病解释而被转诊进行精神科评估,随后被诊断为SPS的患者。本病例报告的目的是引起对SPS精神症状表现的关注,并强调在CD的鉴别诊断中进行全面精神科和神经科检查(包括脑成像和电生理研究)的重要性。