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|LETTER TO EDITOR
|Year : 2022 | Volume
| Issue : 2 | Page : 810-811
An Unusual Patient with Acute Multiple Cranial Palsy, Tongue Fasciculations, and Proximal Weakness
Ravindra K Garg, Sorabh Gupta, Imran Rizvi, Hardeep S Malhotra, Neeraj Kumar, Ravi Uniyal
Department of Neurology, King George's Medical University, Lucknow, Uttar Pradesh, India
|Date of Submission||19-Sep-2018|
|Date of Decision||14-Mar-2019|
|Date of Acceptance||17-Mar-2019|
|Date of Web Publication||3-May-2022|
Dr. Ravindra K Garg
Department of Neurology, King George's Medical University, Lucknow - 226 003, Uttar Pradesh
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Garg RK, Gupta S, Rizvi I, Malhotra HS, Kumar N, Uniyal R. An Unusual Patient with Acute Multiple Cranial Palsy, Tongue Fasciculations, and Proximal Weakness. Neurol India 2022;70:810-1
|How to cite this URL:|
Garg RK, Gupta S, Rizvi I, Malhotra HS, Kumar N, Uniyal R. An Unusual Patient with Acute Multiple Cranial Palsy, Tongue Fasciculations, and Proximal Weakness. Neurol India [serial online] 2022 [cited 2022 Jun 25];70:810-1. Available from: https://www.neurologyindia.com/text.asp?2022/70/2/810/344674
Botulism is an infrequently encountered but potentially serious neuromuscular disorder. Botulism often presents with generalized neuroparalytic syndrome. Cranial musculature is dominantly involved. Some cases of botulism land in to respiratory paralysis and may need ventilatory support. Botulism is caused by bacteria Clostridium botulinum. Foodborne botulism is the commonest type of botulism. Foodborne botulism occurs following ingestion of contaminated food containing preformed botulinum toxin., We are reporting an unusual case of foodborne botulism with some unusual clinical manifestations.
An 18-year-old man came with history of acute-onset abdominal pain, nausea, and vomiting 2 days ago. Patient had dinner in a marriage party and symptoms appeared at midnight. Next morning, patient developed dry mouth, drooping of eyelids, diplopia, hoarseness of voice, and difficulty in swallowing and nasal regurgitation of liquids. On second day, patient developed acute-onset symmetrical quadriparesis. These symptoms progressed further in next 18--20 h and patient was unable to move his limbs and unable to speak. He also had mild respiratory distress. On examination (on day 3rd), patient was afebrile and had pulse rate of 88/min and blood pressure was 118/72 mm of Hg without any postural drop. Respiratory rate was 24/min. On neurological examination, patient was fully alert and oriented. Signs of meningeal irritation were absent. Patient had bilateral ptosis, bilateral complete external ophthalmoplegia, and bilateral lower motor neurone facial palsy. Pupils were dilated and were sluggishly reacting to light [Figure 1]. Gag reflex was sluggish. There was generalized tongue fasciculations [Video 1]. Patient was unable to stand from squatting position. Power was decreased in all four limbs (4/5 on MRC scale). Bulk, nutrition, tone, and all deep tendon reflexes were normal. Sensory examination was normal. Plantar reflexes on both sides were flexor. All his blood biochemical parameters were normal. Cerebrospinal fluid examination was normal. Nerve conduction studies and repetitive nerve stimulation were normal. Magnetic resonance imaging of brain was normal. Patient was subjected to neostigmine test that was also normal. Patient was provided only supportive management. Patient condition rapidly improved within 48 h. Tongue fasciculations had markedly diminished [Video 2]. At discharge from hospital, patient was able to stand from squatting position without support. He had subtle ptosis.
|Figure 1: An 18-year-old man was diagnosed with botulism. He shows bilateral ptosis and bilateral absent nasolabial folds|
Click here to view
Possible differential diagnosis in this patient considered were Guillain--Barré syndrome, myasthenia gravis, Miller--Fisher syndrome, brainstem stroke, and snake bite. However, in view of symmetric, descending paralysis, ptosis, bilateral complete ophthalmoplegia, bilateral facial palsy, swallowing difficulty, dry mouth and heralding gastrointestinal symptoms, we made the diagnosis of foodborne botulism. Normal cerebrospinal fluid, normal electrophysiology, and normal neuroimaging further supported the diagnosis of foodborne botulism.,
In fact, the confirmed diagnosis of botulism requires identification of Clostridium botulinum toxins or spore in vomitus, serum, or stool by the mouse inoculation assay method. We did not perform these tests.
Our patient had unusual diffuse tongue fasciculations. Tongue fasciculations disappeared after patient had recovered. Tongue fasciculations are brief spontaneous contraction of a small number of muscle fibers resulting flickering of movement of tongue. Tongue fasciculations are a characteristic manifestation of anterior horn cell diseases, particularly, amyotrophic lateral sclerosis. In neuromuscular junctional disorders, myasthenia gravis is associated with tongue atrophy and fasciculations., Organophosphates inhibit acetylcholinesterase enzyme, which results in the accumulation of acetylcholine at peripheral nicotinic and muscarinic receptors. Fasciculations, in organophosphate poisoning result from increased activity of nicotinic receptors at the level of neuromuscular junction. Among snakes of Elapidae group, Cobra venom contains postsynaptic neurotoxins, while krait venom contains both postsynaptic and presynaptic toxins. A rapidly progressive descending paralysis is the characteristic feature of elapid snake bite in India. Bilateral ptosis and complete external ophthalmoplegia are other hallmark features. Some of these patients fail to protrude their tongue and may have speaking or swallowing difficulties.
In botulism, the defect lies at the presynaptic region of neuromuscular junction. The botulinum toxin hampers the release of acetylcholine at cholinergic nerve terminals. So, it is difficult to explain the reasons for tongue fasciculations in our case. A compilation of clinical data from 332 botulism cases, authors could not find tongue fasciculation even in single case. After extensive search of literature, we came with a single report describing generalized fasciculations in botulism. Possible reason of fasciculation in botulism is either denervation of lingual muscles or unstable neuromuscular junction function.
In conclusion, this was an unusual case of foodborne botulism as patient had diffuse tongue fasciculations.
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There are no conflicts of interest.
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