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Porencephaly and psychosis: a case report and review of the literature
© Douzenis et al; licensee BioMed Central Ltd. 2010
Received: 8 October 2009
Accepted: 2 March 2010
Published: 2 March 2010
Malformations of the cerebral cortex are often associated with developmental delay and psychoses. Porencephaly is a rare congenital disorder of central nervous system involving a cyst or a cavity filled with cerebrospinal fluid, in brain's parenchyma.
We present a 25 years old woman with her first psychotic episode. She also suffers from porencephaly in the frontotemporal lobes region. It is emphasized that the two consistently abnormal brain regions in schizophrenia research had significant damage in this patient since birth. There is a total of only five cases of schizencephaly or porencephaly associated with psychosis in the scientific literature. Their clinical characteristics as well as the imaging results are described.
It is unclear if porencephaly and psychosis concur by chance or are causally related. The area where the porencephalic cysts appear seems to be of relevance. This case highlights the need for further research.
Malformations of the cerebral cortex are often associated with developmental delay and psychoses. Porencephaly is an extremely rare congenital disorder of the central nervous system involving a cyst or a cavity filled with cerebrospinal fluid, in the brain's parenchyma. It is caused by either local damage from ischemia in the brain hemisphere, or most commonly, hemorrhage after birth. It can also occurs as a consequence of abnormal development before birth (these are less common cases) [1, 2].
Congenital brain lesions include two types of porencephaly: genetic porencephaly: Genetic porencephaly resulting from maldevelopment during early neuronal migration and encephalophaloplastic porencephaly, which is late prenatal or perinatal vascular lesion due to arterial ischemic stroke or venous thrombosis. Porencephalic cysts can be located in any lobe or lobes of the two brain hemispheres .
Prefrontal cortex and limbic system hypotheses are the predominant neuroanatomical hypotheses of psychosis. Decreased prefrontal gray or white matter volumes, or disturbed prefrontal metabolism and blood flow. As well as decreased hippocampal and entothinal cortex volume, in psychotic patients, have been demonstrated. All these are strong indications that prefrontal cortical and medial temporal regions are associated with psychosis [4–6].
A 25-year-old woman presented at the emergency department of the 2nd Psychiatry Department in Attikon University General Hospital with psychotic symptoms. She was accompanied by her mother and brother. There was no previous psychiatric history. During the last three days before admission, she was frightened, couldn't sleep properly and said that people talked to her through the television set. On the day of her admission, she stayed home, closed the windows and frequently called her husband at work, asking for help, because something "very bad" would happen. Her husband tried to calm her, but that was impossible. When he arrived home she was lying in bed and didn't offer any explanations for her behavior.
On mental state examination, the patient was oriented in person, place and time. She expressed persecutory delusions that were related to violent incidences (riots) that occurred the previous days in Athens. Her thought content was characterized by delusions of persecution and reference. Her speech was interrupted and she appeared to experience thought blocking. She did not admit to auditory hallucinations. Patient's affect was subjectively anxious and fearful but objectively her affect was blunted and she did not display any insight into her condition. She had psychomotor retardation and her speech was slow. She was not suicidal. She told us she suffered from insomnia the last days before admission and she was co-operative, accepting admission. Upon admission PANSS scores were: Positive: +17, Negative:-22, General Psychopathology: 35 Neurological examination revealed right arm weakness (proximal 3|5, distal 2+/5 according to the MRC scale of evaluation), pyramidal type rigidity with increase of deep tendon reflexes, muscle atrophy and stereoagnosia of the same arm. The Mini-Mental State Examination was normal (30/30). A neuropsychological examination showed few alterations, with impairment of verbal memory, attention and ability to plan (WAIS: 64, Verbal: 69, Performance: 63).
She had no past psychiatric history or family psychiatric history. According to her medical history, she suffers from porencephaly located in the front-temporal lobes region since birth. The patient had no speech development problems or severe mental retardation that is often associated with porencephaly. However, she had a slight spastic paresis in her right arm. The patient never received antiepileptic treatment and no physiotherapy was ever suggested for her arm spasticity and movement difficulties. According to the relatives, neurosurgery assessment was never suggested to them. When inpatient a referral to the neurosurgeons was made but after inspecting her brain MRI and bearing in mind that there were no clinical signs of increased CSF pressure it was felt that no further assessment was needed. Generally, treatment of porencephaly aims at alleviating symptoms as there is no treatment to induce brain growth in the missing sections and that can include antiepileptic medication, physiotherapy or a shunt to remove excess cerebrospinal fluid .
Haematological and biochemistry blood test results, thyroid tests, toxicological tests, gonathotropins and cortizol levels were within normal range and did not reveal any other related medical condition.
The patient was not very social as a child; she had only few friends, however she managed to complete secondary education. She grew up in a small village and lived there up until she was 23. She had no intimate relationships until she met his husband and left with him for Athens. She kept their house but her husband did all external jobs and she never left home on her own. Few days before her illness, there was an argument and the husband threatened to leave.
Antipsychotic agents which are strong blockers of D2 receptors were excluded because of her possible vulnerability to extrapyramidal symptoms due to the brain damage. Bearing in mind she was underweight, she was started on olanzapine 10 mg, which has been used successfully for the treatment of another patient with porencephaly and psychosis according to the literature . The psychotic symptoms improved progressively during her inpatient stay. It was clear that there was a significant improvement in relation to the delusional persecutory ideas and a complete remission of these symptoms was achieved. PANSS (Positive: +10, Negative:-18, General Psychopathology: 19). Upon discharge there were no signs of psychomotor retardation The patient was discharged after a 2-week inpatient stay and received follow-up outpatient care with psychiatric appointments). After one year of follow-up, psychiatrically she is table and maintains contact; she continues her treatment and is now receiving 5 mgr of Olanzapine. The diagnosis is schizophrenia paranoid type or psychotic disorder due to a general medical condition. (DSM-IV TR).
The present case had clinical manifestation of porencephaly, i.e. mild mental retardation and spastic paresis in her left arm accompanied by motor impairment. However, this patient did not have speech development problems or seizures. The location of porencephalic cyst, in frontal and temporal lobes, can be associated with psychotic features, or one can suggest that damaged brain regions possibly triggered the patient's potential vulnerability to psychotic symptoms
We reviewed the scientific literature for other cases with porencephaly and psychosis to investigate the above hypothesis. Pae et al. in 2009 report the case of a patient who developed a psychotic episode, possibly, associated with multiple leukoencephalomalacia and Porencephaly changes in the brain cortex. In this case, a 30-year-old woman had persecutory ideas and visual hallucination. Multiple focal leukoencephalomalacia changes in the left frontal lobe, bilateral occipital lobes and left basal ganglia, and a large porencephalic change in the right temporal lobe were found in with (MRI) .
Schizencephaly is also a rare congenital neurodevelopment disorder of brain cortex which is characterized by abnormal slits or clefts in the cerebral hemispheres. That malformation is a form of porencephaly. It appears with paresis, mental retardation and seizures, too . Alexander et al reported two cases with schizencephaly associated with psychosis. The first patient had seizures, mental retardation and psychotic features like delusions and auditory hallucinations. The second patient had monoplegia, mental retardation and delusions. Relan et al presented a case with unilateral schizencephaly cleft associated with biopolar disorder. This patient was overactive and oversocial. She also had mild motor impairment, mental retardation and presented with persecutory ideation and auditory hallucinations .
Cysts on the left temporal lobe have been associated with psychosis. Frontal and especially temporal lobe structure and fuction are consistently implicated in radiological imaging literature (brain imaging research) in schizophrenia . In several MRI studies, medial temporal lobe structures, which include the amygdale, hippocampus, parahipoccampal gyrus and superior temporal gyrus, perform a lot of abnormalities . Especially, deficit in left medial temporal lobe volume is one of the most frequent finding of Morfometry studies in schizophrenia . Alves da Silva et al described the case of a patient with an arachnoid cyst in the left temporal lobe. He had psychotic symptoms such as delusions and hallucinations . Vakis et al reported a case of young woman with a left temporal lobe arachnoid cyst who presented with a psychosis-like syndrome .
Porencephaly and schizencephaly cases in the literature
Number of cases
Pae CU., Kim JH. 2009
Multiple focal leukoencephalomalacia changes in the left frontal lobe, bilateral occipital lobes and left basal ganglia, and a large porencephalic change in the right temporal lobe
Alexander RC et al 1997
unilateral schizencephaly cleft and bilateral schizencephaly cleft
Relan P et al 2002
unilateral schizencephaly cleft
Bipolar Affective Disorder
Douzenis et al 2009
a large porencephalic cyst on the left frontal and temporal lobes.
It is still unclear whether porencephaly and psychosis concur by chance in this case or that there is actually an increased risk for psychosis in patients with porencephaly.
Our review showed that there are only two cases with porencephalic cysts and psychosis as well as 3 cases of schizencephaly. The damaged brain regions in these cases are associated with psychotic symptoms. The presence of neurodevelopment anomalies may have pathoplastic effect on the manifestation of psychosis. We hypothesize that this patient's brain lesions have a crucial influence on her vulnerability to psychotic symptoms. One can assume that even old lesions on the left frontal and temporal lobes can be an additional risk factor for the development of the disorder. She had no past or family psychiatric history and this was her first psychotic episode. Another vulnerability factor is her IQ which was 64, indicating mild mental retardation. Low IQ is associated with a higher incidence of psychotic disorder, than in normal population . This patient's porencephalic cyst extended from left frontal to the left temporal lobe. Lesions in these areas have been associated with psychosis. This case highlights the need that in patients with similar clinical features as described above, radiological examination should be carried out so as to discover damaged brain lesions.
Written informed consent was obtained from the patient in this case report.
We would like to thank the patient and her family for their collaboration.
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