Hefter Dimitri, Topor Cristina E, Gass Peter, Hirjak Dusan
Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Institute of Physiology and Pathophysiology, University of Heidelberg, Heidelberg, Germany.
Front Psychiatry. 2019 Apr 12;10:224. doi: 10.3389/fpsyt.2019.00224. eCollection 2019.
Catatonic phenomena such as stupor, mutism, stereotypy, echolalia, echopraxia, affective flattening, psychomotor deficits, and social withdrawal are characteristic symptoms of both schizophrenia and autism spectrum disorders (ASD), suggesting overlapping pathophysiological similarities such as altered glutamatergic and dopaminergic synaptic transmission and common genetic mutations. In daily clinical practice, ASD can be masked by manifest catatonic or psychotic symptoms and represent a diagnostic challenge, especially in patients with unknown or empty medical history. Unclear diagnosis is one of the main factors for delayed treatment. However, we are still missing diagnostic recommendations when dealing with ASD patients suffering from catatonic syndrome. A 31-year-old male patient without history of psychiatric disease presented with a severe catatonic syndrome and was admitted to our closed psychiatric ward. After the treatment with high-dose lorazepam and intramuscular olanzapine, catatonic symptoms largely remitted, but autistic traits persisted. Following a detailed anamnesis and a thorough neuropsychological testing, we diagnosed the patient with high-functioning autism and catatonic schizophrenia. The patient was discharged in a remitted state with long-acting injectable olanzapine. This case represents an example of diagnostic and therapeutic challenges of catatonic schizophrenia in high-functioning autism due to clinical and neurobiological overlaps of these conditions. We discuss clinical features together with pathophysiological concepts of both conditions. Furthermore, we tackle social and legal hurdles in Germany that naturally arise in these patients. Finally, we present diagnostic "red flags" that can be used to rationally select and conduct current recommended diagnostic assessments if there is a suspicion of ASD in patients with catatonic syndrome in order to provide them with the most appropriate treatment.
紧张症现象,如木僵、缄默、刻板动作、模仿言语、模仿动作、情感平淡、精神运动迟缓及社交退缩,是精神分裂症和自闭症谱系障碍(ASD)的特征性症状,提示存在重叠的病理生理相似性,如谷氨酸能和多巴胺能突触传递改变以及常见基因突变。在日常临床实践中,ASD可能被明显的紧张症或精神病性症状掩盖,构成诊断挑战,尤其是在病史不明或空白的患者中。诊断不明确是治疗延迟的主要因素之一。然而,在处理患有紧张症综合征的ASD患者时,我们仍然缺乏诊断建议。一名无精神疾病史的31岁男性患者出现严重的紧张症综合征,被收治入我们的封闭式精神科病房。在使用大剂量劳拉西泮和肌内注射奥氮平治疗后,紧张症症状基本缓解,但自闭症特征持续存在。经过详细的病史询问和全面的神经心理学测试,我们诊断该患者为高功能自闭症合并紧张型精神分裂症。患者使用长效注射用奥氮平后病情缓解出院。该病例代表了由于这些疾病在临床和神经生物学上的重叠,高功能自闭症中紧张型精神分裂症的诊断和治疗挑战。我们讨论了这两种疾病的临床特征以及病理生理概念。此外,我们还解决了在德国这些患者自然出现的社会和法律障碍。最后,我们提出了诊断“红旗”,如果怀疑紧张症综合征患者患有ASD,可用于合理选择和进行当前推荐的诊断评估,以便为他们提供最合适的治疗。