Manganese and acute paranoid psychosis: a case report
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Manganese regulates many enzymes and is essential for normal development and body function. Chronic manganese intoxication has an insidious and progressive course and usually starts with complaints of headache, fatigue, sleep disturbances, irritability and emotional instability. Later, several organ systems may be affected and, due to neurotoxicity, an atypical parkinsonian syndrome may emerge. With regard to neuropsychiatry, an array of symptoms may develop up to 30 years after intoxication, of which gait and speech abnormalities, cognitive and motor slowing, mood changes and hallucinations are the most common. Psychotic phenomena are rarely reported.
We describe the case of a 49-year-old Caucasian man working as a welder who was referred to our facility for evaluation of acute paranoid psychotic behavior. Our patient's medical history made no mention of any somatic complaints or psychiatric symptoms, and he had been involved in a professional career as a metalworker. On magnetic resonance imaging scanning of his brain, a bilateral hyperdensity of the globus pallidus, suggestive for manganese intoxication, was found. His manganese serum level was 52 to 97 nmol/L (range: 7 to 20 nmol/L). A diagnosis of organic psychotic disorder due to manganese overexposure was made. His psychotic symptoms disappeared within two weeks of treatment with low-dose risperidone. At three months later, serum manganese was decreased to slightly elevated levels and the magnetic resonance imaging T1 signal intensity was reduced. No signs of Parkinsonism were found and a definite diagnosis of manganese-induced apathy syndrome was made.
Although neuropsychiatric and neurological symptoms caused by (chronic) manganese exposure have been reported frequently in the past, in the present day the disorder is rarely diagnosed. In this report we stress that manganese intoxication can still occur, in our case in a confined-space welder, and may present clinically with a paranoid psychotic state that necessitates a rapid diagnostic procedure in order to avoid the permanent structural brain damage that may occur with chronic exposure.
KeywordsRisperidone Globus Pallidus Paranoid Ideation Atypical Parkinsonian Syndrome Structural Brain Damage
Manganese (Mn) is an essential trace element that regulates and binds to many enzymes throughout the body. In cases of overexposure via inhalation or ingestion, Mn is highly toxic for several organ systems. Mn crosses the blood-brain barrier by the same mechanism that iron does. A peculiar neurological picture similar to Parkinson's shaking palsy due to Mn intoxication was first reported in 1837 . In the first post-war decades of the 20th century, Mn intoxication was documented to occur primarily in miners and welders, manifesting as increased rates of, for example, digestive tract and lung cancer, liver cirrhosis and heart disease. The most common somatic sequelae are hypertension and increased heart rate due to blocking of calcium channels by Mn, elevated cholesterol levels following reduced conversion of cholesterol to bile acids and decreased fertility in men as well as increased fetal abnormalities .
With respect to the central nervous system, Mn overexposure initially induces non-specific symptoms such as headache, asthenia, irritability, fatigue, sleep disturbances and emotional instability. Later, a neurodegenerative syndrome with psychiatric symptoms, called manganism, may develop that is characterized by speech, gait and balance problems on the one hand, and obsessive-compulsive behaviors, hostility, mood changes, psychotic experiences such as hallucinations and paranoid ideation, and reduced cognitive flexibility on the other hand [3, 4, 5].
In a previous report by Kim et al., an magnetic resonance imaging (MRI) scan of an Mn-overexposed patient showed a regional distribution of high signal intensities in the globus pallidus (100%), midbrain (80%), pituitary gland (43%) and putamen (16%) . The increased signal intensities in the nigrostriatal structures, particularly the globus pallidus, are best demonstrated on T1-weighted images and correlate positively with the Mn concentration in the blood [7, 8]. These findings correspond with the neurological syndrome of atypical parkinsonism that comprises, apart from general bradykinesia, rigidity and kinetic tremor, frequent dystonias and a specific cock-walk gait with a tendency to fall forward . In contrast to the findings in patients with Parkinson's disease, positron emission tomography (PET) studies in patients exposed to Mn in general show no dopaminergic abnormalities . Single-photon emission computed tomography (SPECT) images of dopamine transporter (DAT) also demonstrate an overall normal DAT uptake in the striatum . More recent findings in non-human primates suggest that chronic Mn exposure induces a cellular stress response leading to neurodegenerative changes in the frontal cortex that coincide with subtle cognitive deficits [12, 13, 14].
In this report, we describe the case of a middle-aged man referred to our out-patient clinic for psychiatric evaluation because of an acute paranoid psychosis.
Our patient was a 49-year-old Caucasian man who's educational history showed he had completed primary school only. He had been employed in a professional capacity as a metalworker and welder for many years. His somatic history mentioned only slight hypertension, for which he was treated with 25 mg hydrochlorothiazide daily. He was referred for paranoid ideation, thoughts of reference, sleep disturbances and bizarre behaviors. A provisional diagnosis of acute paranoid psychosis was made and our patient was subsequently treated with 2 mg risperidone daily. Within two weeks the psychotic symptoms gradually disappeared and the dose of risperidone was lowered to 1 mg daily. Physical and neurological assessments did not reveal any abnormalities. Routine hematological and biochemical tests, including hemoglobin, lipoprotein profile and fasting glucose, were all within normal ranges. Borrelia and lues serology results were negative. Use of medications including over the counter preparations and illicit drugs were excluded by systematic evaluation.
At three months after the initial referral, a follow-up MRI of the brain again showed enhanced T1 signal intensity in the same areas, but clearly to a lesser extent. The serum Mn concentration had decreased to high normal levels (31 to 36 nmol/L). On neuropsychiatric evaluation, our patient presented with a flat affect and mental dullness. There was a marked discrepancy between his appearance and his stated age. A detailed neurological examination disclosed, apart from a sluggish and indifferent attitude, no abnormalities, especially no signs or symptoms indicative for a parkinsonian syndrome. With respect to psychopathology, using the elements of the Comprehensive Psychiatric Rating Scale his thinking was slow and rigid and, apart from irritability and impulsivity, no formal psychiatric disturbances could be detected. His behavior was dominated by loss of interest in daily activities and social withdrawal as well as a lack of concern about his personal life and intentions. A neuropsychological assessment demonstrated a total IQ of 62 (Kaufman Adult Intelligence Test), which is in agreement with the estimated pre-morbid total IQ of 57 (National Adult Reading Test). There was a slow speed of information processing and a marked cognitive dysfunction with respect to attention, memory (learning and retrieval) and executive functioning (flexibility and shifting).
At follow-up after six months, a further neuropsychiatric examination disclosed findings similar to those obtained previously and treatment with risperidone was discontinued. His wife reported that the changes in his behavior, mood and interests had started insidiously several years before the first psychotic symptoms. A final diagnosis of apathy syndrome caused by chronic overexposure to Mn was formulated. Subsequently, psychosocial supportive therapy was given and our patient will be re-examined twice yearly in order to monitor the potential development of parkinsonian symptoms.
In our 49-year-old patient, a bilaterally increased signal intensity in the globus pallidus on T1-weighted MRI was found. It appeared to be caused by overexposure to Mn as demonstrated by an elevated serum concentration of Mn. Therefore, a diagnosis of organic psychotic disorder/apathy syndrome due to Mn intoxication was made. This diagnosis was supported by the decrease of serum levels of Mn and the reduction of bilateral globus pallidus T1 signal intensities over a period of three months. Extensive investigation of our patient's environment revealed no potential sources for Mn exposure other than occupational exposure.
For several decades it has been known that once the neuropathology is clearly expressed at the clinical level, Mn-caused damage to the central nervous system is essentially irreversible and often evolutive . Eventually, an atypical parkinsonian syndrome may emerge that is characterized by gait and balance problems, dysarthria and absence of rest tremor, and points at a striatal-pallidal degeneration . Whether recurrent low-dose occupational exposure to Mn causes early brain damage is still controversial .
Several studies have replicated the observation that the nigrostriatal dopaminergic system is essentially intact in manganism, which has become evident from normal PET and DAT-SPECT findings. Thus, in cases of high T1 signal in patients with a history of Mn exposure in whom a normal PET/SPECT uptake is found, a diagnosis of Mn-induced parkinsonism is justified. If PET/SPECT uptake is reduced and MRI shows no abnormalities, a diagnosis of idiopathic Parkinson's disease should be made .
Although the results from a few older reports are suggestive for some efficacy of treatment with L-3,4-dihydroxyphenylalanine (L-dopa) or 5-hydroxytryptophan in Mn-induced parkinsonism, no effect could be demonstrated in the only placebo-controlled study . This unresponsiveness to (L-dopa) is most likely related to the difference in the pathophysiology between idiopathic and Mn-induced parkinsonism. It has been repeatedly shown that Mn accumulation in the brain is not associated with degeneration of nigrostriatal dopaminergic neurons .
With respect to possible ways to reduce Mn accumulation in brain structures in order to prevent neurological damage, chelating agents such as ethylenediaminetetra-acetic acid (EDTA), have been reported to possibly generate some positive effects in the early stages of poisoning, although sometimes only temporarily. In case of structural brain damage, however, chelating therapy cannot be expected to bring about any improvement . In the latter condition, experimental treatment with para-aminosalicylic acid (PAS), originally used for the treatment of tuberculosis, has been applied with promising alleviation of neurological symptoms .
With regard to the neuropsychiatric and psychological effects of Mn overexposure, several domains of dysfunction can be delineated such as: emotional instability with irritability, anxiety, impulsivity and hostility; psychotic symptoms such as paranoid ideation and hallucinations; compulsive behaviors; and cognitive dysfunctions, particularly slowing of information processing, reduced mental flexibility and impaired attention and learning . For these areas of dysfunction, no specific psychopharmacological strategies can be recommended other than the regular treatment modalities [4, 9].
To the best of our knowledge, this is the first report of Mn-induced paranoid psychosis due to confined-space welding. The occurrence of subacute psychotic symptoms in the absence of a psychiatric history may point towards occupational diseases that in the modern world are now rare. In the case of Mn exposure, treatment with EDTA may be effective in the early stages. Later, however, when the neurodegenerative parkinsonian syndrome has become irreversible and sometimes progressive without any further Mn exposure, no therapeutic options remain. Therefore, prevention of Mn intoxication should be the primary target.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors are indebted to PPA Lenssen, neurologist at the general hospital Elkerliek in Helmond, The Netherlands, and to Dr BPC van de Warrenburg, neurologist and Dr C Kramers, internist/clinical pharmacologist at the Radboud University Medical Centre in Nijmegen, The Netherlands, for their skillful assistance.
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