一例伴有Cotard综合征的神经纤维瘤病1(NF1)病例报告

IF 0.3 Q4 PSYCHIATRY
Saumitra Nemlekar, Dhruv Bardolia, Urvish Jaganiya, R. Mehta, K. Dave
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引用次数: 1

摘要

1型神经纤维瘤病是一种神经皮肤常染色体显性遗传病,常与各种精神疾病相关。科塔尔综合征是一种罕见的神经精神障碍,见于各种神经和心理疾病。神经纤维瘤病的复杂病程使个体倾向于更高的身体和精神发病率。我们在此报告一例神经纤维瘤病患者的科塔尔综合征。这名患者据称有自残史,情绪普遍悲伤;诊断为复发性抑郁症,当前严重发作伴精神病性特征。患者给予口服精神药物治疗,治疗效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A unique case of neurofibromatosis 1 (NF1) with Cotard syndrome – A case report
Neurofibromatosis type 1 is a neuro-cutaneous autosomal dominant disorder that is often associated with vari-ous psychiatric disorders. Cotard syndrome is a rare neuropsychiatric disorder seen in a variety of neurological and psychological illnesses. The complex course of the neurofibromatosis predisposes the individual towards higher physical and psychiatric morbidity. Here we present a case of Cotard syndrome in a patient with neurofibromatosis. The patient was brought with an alleged history of self-harm and pervasive sadness of mood; a diagnosis of recurrent depressive disorder current episode severe with psychotic features was made. Patient was treated with oral psychotropic agents and responded well to the treatment.
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CiteScore
1.20
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