Blanc F, Berna F, Fleury M, Lita L, Ruppert E, Ferriby D, Vermersch P, Vidailhet P, de Seze J
Service de neuropsychologie, département de neurologie, hôpitaux universitaires de Strasbourg, 1, place de l'Hôpital, 67091 Strasbourg, France.
Rev Neurol (Paris). 2010 Jan;166(1):39-48. doi: 10.1016/j.neurol.2009.04.014. Epub 2009 Sep 6.
Psychotic symptoms are not readily recognized in multiple sclerosis, especially at the beginning of the disease.
We report the cases of four patients who developed psychotic symptoms that led to the diagnosis of multiple sclerosis. We describe the psychiatric and neurological features, MRI findings, clinical outcome and treatment.
Two patients developed persecutory delusions, one presented a manic episode and the fourth melancholia with catatonia. Mean age was 39 years (range 20-49 years). Two patients had a personal history, but none a familial history of psychiatric disease. Examination of the cerebrospinal fluid revealed an oligoclonal pattern in all patients. All patients fulfilled Barkhof's MRI criteria. Three have had brain MRI with injection during psychotic symptoms. In these three cases, a frontal lesion appeared. The patient with catatonia also had a new lesion in the cerebellum and in the brainstem. All patients needed a "psychiatric" treatment, including antipsychotics. The psychiatric event lasted three months for two patients and the two others experienced relapse.
Acute psychiatric symptom may reveal multiple sclerosis at the beginning of the disease. Frontal lobe localization is suggested. We propose that a psychotic event may correspond to a multiple sclerosis event.
精神病性症状在多发性硬化症中不易被识别,尤其是在疾病初期。
我们报告了4例出现精神病性症状并最终诊断为多发性硬化症的患者病例。我们描述了其精神和神经学特征、MRI检查结果、临床结局及治疗情况。
2例患者出现被害妄想,1例表现为躁狂发作,第4例为伴有紧张症的忧郁症。平均年龄为39岁(范围20 - 49岁)。2例患者有个人精神病史,但均无精神病家族史。脑脊液检查显示所有患者均有寡克隆带型。所有患者均符合巴霍夫MRI标准。3例患者在出现精神病性症状期间进行了增强脑MRI检查。在这3例中,均出现额叶病变。伴有紧张症的患者在小脑和脑干也有新发病变。所有患者均需要“精神科”治疗,包括使用抗精神病药物。2例患者的精神症状持续了3个月,另外2例复发。
急性精神症状可能在疾病初期揭示多发性硬化症。提示额叶定位。我们认为精神病性事件可能与多发性硬化症事件相关。