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儿童期起病精神分裂症和22q11.2缺失综合征中海马旋转异常这一罕见神经放射学表现:一例病例报告及文献简要综述

An uncommon neuroradiological finding of hippocampal malrotation in childhood onset schizophrenia and 22q11.2 Deletion Syndrome: a case report and a brief review of the literature.

作者信息

Giardino Maria, Peluso Francesca, Daolio Omar, Bellini Melissa, Ambrosini Enrico, Zito Matteo, Squarcia Antonella

机构信息

Child Neuropsychiatry Unit, Azienda USL di Parma, Parma, Italy.

Medical Genetics Unit, Maternal and Child Health Department, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

出版信息

Eur Child Adolesc Psychiatry. 2025 Jan;34(1):363-368. doi: 10.1007/s00787-024-02569-6. Epub 2024 Aug 20.

Abstract

Childhood Onset Schizophrenia is a rare neuropsychiatric disorder significantly associated with 22q11.2 Deletion Syndrome. We describe a male patient, followed from childhood to adolescence, who exhibited premorbid impairments in language, learning and social abilities, along with comorbid anxiety disorders. Over time, he gradually developed Childhood Onset Schizophrenia, with neuroradiological findings of white matter hyperintensities, a dysmorphic corpus callosum and Hippocampal Malrotation. These findings were observed in the context of a genetic diagnosis of 22q11.2 Deletion Syndrome, despite the absence of the most common congenital malformations and clinical conditions typically associated with this syndrome. A remarkable aspect of this case report is the emphasis on the importance of suspecting 22q11.2 Deletion Syndrome even in cases where only the neuropsychiatric phenotype of Childhood-Onset Schizophrenia and structural brain alterations, is present. While abnormalities of white matter and corpus callosum are associated with schizophrenia in patients with 22q11.2 Deletion Syndrome, Hippocampal Malrotation is more frequently described in patients with epilepsy and prolonged febrile seizures. Recently, only 10 adult patients with 22q11.2 Deletion Syndrome have been reported to have Hippocampal Malrotation, six of whom were affected by schizophrenia, with or without epilepsy. Our case report aims to extend the neuroradiological findings associated with 22q11.2 Deletion Syndrome and Schizophrenia, including Hippocampal Malrotation. This is the first case report in which Hippocampal Malrotation has been described in Childhood Onset Schizophrenia and 22q11.2 Deletion Syndrome. We suggest that patients with Hippocampal Malrotation and Childhood Onset Schizophrenia, should have a chromosomal microarray performed to screen for 22q11.2 Deletion Syndrome.

摘要

儿童期起病的精神分裂症是一种罕见的神经精神障碍,与22q11.2缺失综合征显著相关。我们描述了一名从儿童期到青少年期接受随访的男性患者,他在病前语言、学习和社交能力方面存在缺陷,同时伴有焦虑症。随着时间的推移,他逐渐发展为儿童期起病的精神分裂症,神经放射学检查发现有白质高信号、胼胝体畸形和海马旋转不良。尽管没有与该综合征相关的最常见先天性畸形和临床症状,但这些发现是在22q11.2缺失综合征的基因诊断背景下观察到的。本病例报告的一个显著特点是强调,即使在仅出现儿童期起病的精神分裂症神经精神表型和脑结构改变的情况下,也应怀疑22q11.2缺失综合征。虽然白质和胼胝体异常与22q11.2缺失综合征患者的精神分裂症有关,但海马旋转不良在癫痫和长时间热性惊厥患者中更为常见。最近,仅有10例成年22q11.2缺失综合征患者被报道有海马旋转不良,其中6例患有精神分裂症,伴或不伴有癫痫。我们的病例报告旨在扩展与22q11.2缺失综合征和精神分裂症相关的神经放射学发现,包括海马旋转不良。这是第一例在儿童期起病的精神分裂症和22q11.2缺失综合征中描述海马旋转不良的病例报告。我们建议,患有海马旋转不良和儿童期起病精神分裂症的患者,应进行染色体微阵列检测以筛查22q11.2缺失综合征。

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