Chabrol H, Bonnet D
CHS Gérard Marchand, Toulouse.
Encephale. 1995 Nov-Dec;21(6):477-80.
The author report a case of Capgras' syndrome in a 12-years-old girl, who had been hospitalized for attacks of abdominal pain. These symptoms had gone on for two years and led twice to surgical interventions which did not find any organic etiology. Interviews with the girl showed that the abdominal pains were related to symptoms of typical panic attacks which lasted about 20 minutes. In some on them, she experienced multiple autoscopy and the "illusion des sosies", described by Capgras. Long-term evolution showed that Capgras' syndrome disappeared with improvement of the panic attacks, but ten years later the patient is still suffering from generalized anxiety. To our knowledge, no case, even in adult patients, was previously described in the context of panic attacks. Furthermore, Capgras' syndrome is particularly rare at adolescence. Our review of literature exhibits only 19 cases under 18. Diagnosis was available in 16 cases, and consisted of schizophrenia or schizophreniform psychosis in 62.5% of the cases. The others involved acute psychosis (2 cases), post-partum psychosis (1 case), drug-induced-psychosis (1 case), psychotic major depression (1 case), and post-varicella encephalitis (1 case). The doubles (out of the 15 cases where relevant detail is available) included at least a parent in 92.9% of patients, a brother or sister in 35.7%, a member of the medical team in 21.4% and a grand-parent in 14.3%.
作者报告了一例12岁女孩的卡普格拉综合征,该女孩因腹痛发作入院。这些症状持续了两年,两次导致外科手术干预,但未发现任何器质性病因。与该女孩的访谈显示,腹痛与典型惊恐发作的症状有关,惊恐发作持续约20分钟。在其中一些发作中,她经历了多次自体幻觉和卡普格拉所描述的“替身错觉”。长期演变表明,随着惊恐发作的改善,卡普格拉综合征消失,但十年后患者仍患有广泛性焦虑症。据我们所知,以前即使在成年患者中,也没有在惊恐发作的背景下描述过这种病例。此外,卡普格拉综合征在青少年中尤为罕见。我们对文献的回顾仅显示19例18岁以下的病例。16例有诊断结果,其中62.5%为精神分裂症或精神分裂样精神病。其他病例包括急性精神病(2例)、产后精神病(1例)、药物性精神病(1例)、重度抑郁伴精神病性症状(1例)和水痘后脑炎(1例)。在可获得相关细节的15例病例中,“替身”包括至少一名父母的占患者的92.9%,兄弟姐妹的占35.7%,医疗团队成员的占21.4%,祖父母的占14.3%。