Takayasu's disease presenting as convulsive syncope which had been misinterpreted as epilepsy: a case report
© Menon and Himabindu; licensee BioMed Central Ltd. 2010
Received: 23 October 2009
Accepted: 2 November 2010
Published: 2 November 2010
Takayasu's arteritis is a chronic vasculitis mainly involving the aorta and its main branches. The disease has protean clinical manifestation ranging from asymptomatic to catastrophic illness.
A 19-year-old woman of Asian origin was referred to our neurology out-patient department for the management of refractory seizures. She reported several episodes of a loss of consciousness with tonic posturing when she assumed an upright position, which was accompanied by constitutional symptoms. A clinical examination showed orthostatic hypotension and an investigation confirmed the diagnosis of Takayasu's disease with presentation as convulsive syncope.
Our case highlights the importance of a thorough clinical history and physical examination in order to distinguish events mimicking epileptic seizure. We also describe an unusual presentation of Takayasu's disease with convulsive syncope and systemic constitutional symptoms.
Takayasu's arteritis (TA) is an inflammatory and stenotic disease of medium-sized and large-sized arteries characterized by a strong predilection for the aortic arch and its branches. Symptoms of the disease start with non-specific constitutional symptoms in the first stage to organ specific ischemic symptoms in the second stage. Occasionally there is no clear demarcation between stages, and diagnosis can be difficult in such a setting. We report the case of a 19-year-old woman who was referred to our neurology out-patient department for recurrent episodes of loss of consciousness and systemic constitutional symptoms.
A 19-year-old Asian woman was referred to the department of neurology for the management of recurrent seizures. She had been having recurrent episodes of a loss of consciousness. On detailed enquiry she revealed that these episodes were present immediately on changing to an upright posture from a lying position. She would lose consciousness, become pale, and fall to the ground. She would then experience tonic posturing of the limbs lasting for a few seconds. She would immediately regain consciousness in the supine position, with no postictal drowsiness. There were several similar episodes a day, and this had persisted for the last three months. Her symptoms persisted even after treatment with phenytoin, phenobarbitone, and sodium valproate, with no decrease in the frequency of episodes. She also complained of fatigue, malaise, myalgia, giddiness, fever, decreased appetite and weight loss over the preceding three months. Her medical history was not significant. There was no previous or family history of tuberculosis.
Physical examination revealed a thin built, frail and anxious patient. She was afebrile. Her radial pulses were very feeble while lower limb pulses felt normal. Her bilateral carotid pulses were also feeble. Upper limb blood pressure (BP) was measured (with difficulty) as being 72/58 mmHg in both upper limbs in a supine position. Standing BP was 50/48 mmHg in the upper limbs, suggestive of orthostatic hypotension. Lower limb blood pressures were130/70 mmHg bilaterally. The results of cardiac examination were normal. Her higher mental functions and fundi were normal. There was no cranial nerve, motor or sensory deficit.
An axial reconstruction image (Figure 2C) showed diffuse wall thickening of arteries with luminal narrowing.
Our patient was diagnosed as having TA, fulfilling four of the six criteria for diagnosis: development of symptoms or findings related to TA at age ≤40 years, decreased pulsation of one or both brachial arteries, arteriographic narrowing or occlusion of the primary branches of the aorta, and a difference of >10 mmHg in systolic blood pressure between arms . The results of laboratory investigations for anemia, elevated ESR and C-reactive protein were suggestive of active disease. She was hospitalized and prescribed complete bed rest. Prednisolone (40 mg/day) along with antacids were given. Our patient started feeling better after a week and was therefore gradually mobilized. She did have episodes of giddiness, but there was no loss of consciousness or tonic posturing of limbs. She was discharged after two weeks. After a year, at follow-up she had made a clinical improvement with no constitutional symptoms or syncopal seizures but her radial pulses remained feeble. There was no evidence of postural hypotension.
TA is a chronic vasculitis that mainly involves the aorta and its main branches (the brachiocephalic, carotid, subclavian, vertebral and renal arteries), as well as the coronary and pulmonary arteries. The disease is most commonly seen in Asian and Latin American countries . The incidence of TA is about 2 in 10,000 person-years . The female/male ratio varies from 9:1 in reports from Japan to 1.3:1 in India . The underlying pathology is inflammation leading to stenosis, blockage or aneurysm formation. The disease is also called the pulseless disease because of the difficulty in detecting the peripheral pulses.
The etiology of the disease is still poorly understood. The clinical presentation is widely heterogeneous depending on the involvement of the vessels. The disease has three stages, in which there is an initial pre-pulseless stage predominated by systemic constitutional symptoms. As a result of the non-specificity of the symptoms the diagnosis is often delayed until the next stage of vascular insufficiency. The second stage may be devoid of any signs of inflammation. Hypertension due to renal artery stenosis, retinopathy, aortic regurgitation, aneurismal enlargement of aorta, congestive cardiac failure, postural dizziness, amaurosis, transient ischemic attacks and stroke are some of the presenting features in the second stage. The third stage is the stage of quiescence. Collateral circulation develops because of the chronic nature of the illness. Neurological manifestation is seen in about 20% of cases. The initial manifestations are predominantly ischemic in nature because of the stenosis of the vessels. Seizures as an initial manifestation have been reported but are rare . Syncopal seizures have not been reported. A MeSH database searches with the headings 'Syncope', 'convulsion' and 'Takayasu's arteritis' did produce any reported studies.
Our patient had stenosis of the major branches of the aorta, brachiocephalic, subclavian and left common carotid artery. The cerebral perfusion was being maintained by the collateral circulation. The differential diagnosis of episodic neurological dysfunction included a vast range of disorders. The loss of consciousness, with tonic posturing, led to the misdiagnosis of epilepsy. However, these symptoms were suggestive of convulsive syncope because: all episodes had a postural component, episodes were only for few seconds and there was no postictal drowsiness, our patient immediately regained consciousness in the recumbent position and documented orthostatic hypotension was found on examination. Syncope is transient loss of consciousness due to cerebral hypoxia. This may be accompanied with convulsive episodes. Convulsive syncope merely represents a variant of syncope, which is accompanied by tonic or myoclonic activity.
The differential diagnoses of TA include tuberculosis, temporal arteritis, atherosclerosis, fibro muscular dysplasia and syphilitic aortitis. Apart from syphilitic aortitis, which affects the aorta with calcification, all the other differentials have a predilection for other vessels. The gold standard of investigation was considered to be angiography, but non-invasive Doppler and MRA can provide equally good results .
In the active stage of the disease, judged by systemic symptoms, glucocorticoids are the mainstay of treatment. This is thought to halt the inflammation and further stenosis in vessels. Serological tests have not so far proved helpful in differentiating the active from the inactive stage . Surgery is indicated in certain patients with inactive disease.
Misdiagnosis of epilepsy remains a major clinical problem. We presented this case in order to highlight two findings: the importance of a detailed clinical history and examination, which will help to determine whether or not an epileptic seizure actually occurred in a patient and to differentiate seizure mimics and the absence of stage-wise progression of the symptoms in TA which can create a diagnostic dilemma.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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