Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
© Ramdhani et al. 2010
Received: 19 September 2009
Accepted: 10 September 2010
Published: 10 September 2010
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© Ramdhani et al. 2010
Received: 19 September 2009
Accepted: 10 September 2010
Published: 10 September 2010
This case report describes an extremely rare combination of paroxysmal autonomic instability with dystonia and tuberculous meningitis. Paroxysmal autonomic instability with dystonia is normally associated with severe traumatic brain injury.
A 69-year-old man of Indonesian descent was initially suspected of having a community-acquired pneumonia, which was seen on chest X-ray and computed tomography of the chest. However, a bronchoscopy showed no abnormalities. He was treated with amoxicillin-clavulanic acid in combination with ciprofloxacin. However, nine days after admission he was disorientated and complained of headache. Neurological examination revealed no further abnormalities. A lumbar puncture revealed no evidence of meningitis. He was then transferred to our hospital. At that time, initial cultures of bronchial fluid for Mycobacterium tuberculosis turned positive, as well as polymerase chain reaction for Mycobacterium tuberculosis. Later, during his stay in our intensive care unit, he developed periods with hypertension, sinus tachycardia, excessive transpiration, decreased oxygen saturation with tachypnea, pink foamy sputum, and high fever. This constellation of symptoms was accompanied by dystonia in the first days. These episodes lasted approximately 30 minutes and improved after administration of morphine, benzodiazepines or clonidine. Magnetic resonance imaging showed an abnormal signal in the region of the hippocampus, thalamus and the anterior parts of the lentiform nucleus and caudate nucleus.
In patients with (tuberculous) meningitis and episodes of extreme hypertension and fever, paroxysmal autonomic instability with dystonia should be considered.
Fever is a common symptom in the intensive care unit (ICU) and is often related to infectious diseases, either present on admission or nosocomially acquired. Therefore, if a patient develops fever clinicians will obviously be looking for an infection. Hypertension is another phenomenon that is frequently encountered in ICUs and is often attributed to pain or discomfort of the patient. However, both symptoms, alone or in combination with other symptoms, might be caused by infrequent syndromes. Here, we report a patient with attacks of hypertension, fever and autonomous instability caused by paroxysmal autonomic instability with dystonia (PAID). Infection is an extremely rare cause of this syndrome. However, early recognition will prevent over-treatment with antimicrobial agents.
A 69-year-old man of Indonesian descent was admitted to another hospital with fever and dyspnea. His medical history included tuberculosis in his youth, which was left untreated, ulcerative colitis and a myocardial infarction. His current medication was a beta-blocker, acetylsalicylic acid and azathioprine.
On admission his body temperature was 39.5°C (103°F), and physical and laboratory examination revealed no other abnormalities except for crackles on both sides of the lungs. A chest X-ray showed bilateral nodular changes, which were confirmed by subsequent computed tomography (CT) of the chest. However, a bronchoscopy showed no abnormalities. Cytological examination of sputum was normal. Cultures of blood, sputum, and urine were negative. Auramine, Ziehl-Neelsen stain, and polymerase chain reaction (PCR) for mycobacterium were also negative. The initial screening for tuberculosis was negative and culture results for tuberculosis were not yet available. While waiting for results, anti-microbial treatment was started based upon the suspicion of a community-acquired pneumonia.
The patient was treated with amoxicillin-clavulanic acid in combination with ciprofloxacin. A hypersensitivity pneumonitis caused by azathioprine exposure was also considered and therefore azathioprine was discontinued and prednisone 60 mg a day was started.
Laboratory values at admission in the other hospital (day 1) and after transfer to our hospital (day 16).
4.7 × 109/L
12 × 109/L
4.0-10.0 × 109/L
This case report is remarkable because PAID is rarely encountered in patients with cerebral infections. Autonomic dysfunction is reported in cases of traumatic brain injury (TBI), hydrocephalus, brain tumors, subarachnoid hemorrhage, and intra-cerebral hemorrhage. The clinical manifestations of autonomic dysfunction are hypertension, a temperature above 38.5°C, a pulse of at least 130 beats per minute, a respiratory rate of at least 40 breaths per minute, intermittent agitation, and diaphoresis. This constellation of symptoms is accompanied by dystonia (rigidity or decerebrate posturing for a duration of at least one cycle per day for at least three days). This can be attributed to altered autonomic activity and recently a new term has been put forth that seeks to more precisely characterize this condition: paroxysmal autonomic instability with dystonia (PAID) . While PAID is predominantly associated with TBI, infection is seldom considered to be a cause of PAID .
In 1929 Penfield described a patient with a syndrome called "diencephalic autonomic epilepsy". Signs and symptoms consisted of prodromal restlessness, sudden vasodilatation, sudden rise in blood pressure, lacrimation, diaphoresis, salivation, dilatation or contraction of pupils, sometimes protrusion of eyes, increased rate and pressure of pulse, marked retardation of respiratory rate, elicitation of pilomotor reflex, and rarely loss of consciousness. These features were followed by disappearance of superficial blush and fall of blood pressure, slowing and weakening of pulse, hiccupping, transient shivering, and Cheyne-Stokes respiration. Disturbance of hypothalamic function was considered to be due to a focal epileptic discharge. Autopsy revealed a tumor in the third ventricle . However, later reports of diencephalic seizures did not correlate with electroencephalogram seizure activity, nor were they responsive to anti-convulsants [4–6]. Nowadays the "diencephalic seizures" are considered to constitute a syndrome distinct from PAID .
Hereafter, episodic agitation, diaphoresis, hyperthermia, tachycardia, tachypnea, and rigid decerebrate posturing after severe brain injury were first noted in a report by Strich in 1956 . He called these events "brainstem attacks". Subsequently, this constellation of clinical signs has received a variety of labels, including autonomic dysfunction syndrome, dysautonomia, and sympathetic storms . While PAID is noted in approximately 15 to 33% after brain injury, there seems to be no relation with the severity of brain damage. Neuroimaging revealed more frequent evidence of diffuse axonal injury and brainstem injury in those who developed dysautonomia. Often tachycardia, fever and hypertension are the main presenting signs . Our case illustrates this, as extensor posturing was only present in the first days.
The pathophysiology of PAID can be best explained by dysfunction of autonomic centers in the diencephalon (thalamus or hypothalamus) or their connections to cortical, sub-cortical, and brainstem loci that mediate autonomic function, which leads to loss of control of vegetative functions [1, 5]. The episodic nature of dysautonomia in PAID might be related to triggering events . Changes in intra-cranial pressure or stimulation of muscle mechanoreceptors and manipulation of endotracheal tube, oropharyngeal suction, and pain may precipitate these attacks [6, 9–11]. Indeed, our patient had a slightly raised intra-cranial pressure at the second lumbar puncture. Thermoregulatory dysfunction may also be produced by hypothalamic dysfunction as by the hyper-metabolic state that accompanies sustained muscular contractions. Rigidity and decerebrate posturing are seen experimentally and clinically with lesions in the midbrain, which causes blocking of normal inhibitory signals to pontine and vestibular nuclei .
Differential diagnosis of hypertension and dystonia.
Increased intracranial pressure (ICP)
Non-convulsive epileptic seizures
Paroxysmal autonomic instability with dystonia (PAID)
Renal artery stenosis
All these diseases share some features with PAID. Autonomic dysfunction is associated with increased morbidity. While the length of stay in hospital is not different from those without PAID, the length of stay in rehabilitation services is longer. The risk of myocardial infarction and secondary injury due to hemorrhage or elevated intra-cerebral temperature is of concern. Additionally, PAID is also associated with less favorable functional outcomes.
Treatment of PAID is based on case reports and randomized clinical trials are lacking. Next to the treatment of the underlying cause the central sympathetic pathways may be controlled by morphine, bromocriptine [5, 9, 13, 14], clonidine or a non-selective beta-blocker [6, 13–15]. Benzodiazepines can also be effective, as in our patient [1, 16]. Dantrolene can decrease fever due to prolonged muscle contraction [11, 16].
In this case report PAID was secondary to tuberculous meningitis with infiltration of the thalamus hypothalamus parenchyma. Autonomic instability has only been described once in a two-year-old girl with tuberculous meningitis . However, this girl also had hydrocephalus and bilateral hemorrhagic infarctions in her basal ganglia. Conditions that independently have been associated with PAID. Early recognition is of paramount importance to start treatment in an early stage, but recognition is often difficult, as demonstrated in this case.
PAID is a very rare syndrome in tuberculous meningitis, but recognition and treatment is very important to prevent further complications. In our patient MRI showed abnormalities of the basal nuclei and thalamus-hypothalamus region which may add to previous evidence for the important role of the thalamus in the pathophysiology of PAID.
Written informed consent for publication could not be obtained. All reasonable attempts to gain consent from the patient or their next-of-kin have been made. However, every effort has been made to protect patient anonymity and there is no reason to think that the patient or their family would object to publication.
intensive care unit
paroxysmal autonomic instability with dystonia
polymerase chain reaction
traumatic brain injury
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