A Case of Schizophrenia Accompanied By Lissencephaly

A 32-year-old woman presented with auditory hallucinations and persecutory delusions. She had been suffering from hyperacusis since high school and showed spiritual inclinations, although she had not experienced psychotic symptoms until the age of 32 years. She had no family history of psychiatric disorders, developmental problems, or epilepsy.

The patient was clinically diagnosed with schizophrenia by a psychiatrist 2 weeks before hospitalization, without any diagnostic brain imaging, and she was prescribed an antipsychotic (aripiprazole); however, it did not improve her symptoms. She was admitted to our hospital, and we also diagnosed her with paranoid-type schizophrenia, according to the Diagnostic and Statistical Manual–IV, and we prescribed risperidone, which was increased to 6 mg. After 4 weeks, we changed risperidone to olanzapine and increased the dosage to 15 mg; however, this change was ineffective.

We conducted magnetic resonance imaging (MRI) 5 weeks after hospitalization, because the patient had refused MRI at the time of hospitalization. The MRI showed mild lissencephaly, which was dominant in the temporal and occipital lobes; mild atrophy of the right hippocampus; and hypoplasia of the cerebellum (Figure 1).

Although her electroencephalogram (EEG) did not show convulsive spikes or any other abnormalities except low amplitude, we decided to prescribe sodium valproate on the basis of a similar case report.² After this prescription, her auditory hallucinations and persecutory delusions improved.

Typical lissencephaly is divided into agyria–pachygyria spectrum and cobblestone lissencephaly. Lissencephaly can also be accompanied by cerebellar hypoplasia, which is caused by dysfunction of the reelin gene. Although we were unaware whether our patient had this gene dysfunction, this gene is a controlling factor in cortical structure. This gene also has a possible relationship with schizophrenia;^3,4 however, no cases of lissencephaly with schizophrenia have been reported. Although we had not found any study or case report about schizophrenia associated with lissencephaly, we found one report about schizophrenia associated with schizencephaly.² This case report indicated that the patient was resistant to antipsychotics, and that her psychotic symptoms and abnormal EEG improved with carbamazepine administration, although the patient did not have a history of epilepsy.

MRI is becoming common in clinical psychiatry, and it detects many more cases of cortical dysplasia than expected. Thus, we may encounter more cases of cortical dysplasia with psychosis in the future.