scholarly journals An Atypical Case of Mild COVID-19 Infection with Severe Guillain-Barré Syndrome as Neurological Manifestation

Author(s):  
Debasis Behera ◽  
Ruchi Rekha Behera ◽  
Suman Kumar Jagaty ◽  
Rekha Das ◽  
Rajesh Venkataram ◽  
...  

Abstract Introduction More than 80 million people have been infected with coronavirus disease 2019 (COVID-19) infection worldwide till date with more than 17,00000 fatalities. Although COVID-19 commonly affects respiratory system in the form of cough and dyspnea, a neurotropic presentation has been described in one-third of patients. Objective We report an atypical case of COVID-19 with mild symptoms who presented to our hospital with features suggestive of severe Guillain-Barré syndrome (GBS). Discussion The mechanisms by which severe acute respiratory syndrome coronavirus 2 causes neurologic damage are multifactorial, including direct damage to specific receptors, cytokine-mediated injury, secondary hypoxia, and retrograde travel along nerve fibers. The pathogenesis of GBS secondary to COVID-19 is not yet well understood. It is hypothesized that viral illnesses-related GBS could be mediated due to autoantibodies or direct neurotoxic effects of viruses. Conclusion In this ongoing era of pandemic, it is very important for the clinicians to be aware of association of GBS with COVID-19, as early diagnosis and treatment of this complication could have gratifying results. It is also very important to differentiate GBS from critical illness neuropathy and respiratory distress secondary to COVID-19 itself, as treatment to the above conditions is quite different and inability to correctly diagnose could lead to significant increase in morbidity and mortality.

2019 ◽  
Vol 12 (4) ◽  
pp. e228845 ◽  
Author(s):  
Sajid Hameed ◽  
Sara Khan

Chikungunya (CHIK) viral fever is a self-limiting illness that presents with severe debilitating arthralgia, myalgia, fever and rash. Neurological complications are rare. We present a case of a 36-year-old woman who presented with acute onset progressive difficulty swallowing and left arm weakness. She was diagnosed with CHIK viral fever 4 weeks prior to admission. After investigations, she was diagnosed with a pharyngeal–cervical–brachial variant of Guillain-Barré syndrome. In hospital, she required ventilator support. Her condition improved after five sessions of intravenous immunoglobulin with almost complete resolution within 6 months of symptom onset. With frequent CHIK outbreaks, the neurological complications are increasingly seen in the emergency department. The knowledge of these associations will result in early diagnosis and treatment.


2019 ◽  
Vol 26 (08) ◽  
pp. 1386-1388
Author(s):  
Muhammad Haisum Maqsood ◽  
Kinza Rubab ◽  
Muhammad Zaigham Maqsood

Bickerstaff’s brainstem encephalitis (BBE) is a rare neurological disease characterized by ophthalmoplegia, ataxia and altered sensorium.1 Its etiology is thought to be autoimmune in nature and sometimes certain infections precede illness.2-4 It is a spectrum of illnesses with Guillain-Barre Syndrome (GBS) and Miller Fischer Syndrome (MFS).5-6 We describe an atypical case of BBE which was initially misdiagnosed as meningo-encephalitis. As such, we report this case for its rarity. Informed consent was received from the patient before undertaking and reporting this study.


2015 ◽  
Vol 357 ◽  
pp. e452-e453
Author(s):  
R.V.B. Caldeira ◽  
Y.C. Machado ◽  
M.C. Mota ◽  
T.B. Machado ◽  
N.C.M. Queiroz ◽  
...  

2017 ◽  
Vol 42 ◽  
pp. 275-281 ◽  
Author(s):  
Ugarte Ubiergo Sebastián ◽  
Arenas Villamizar Angel Ricardo ◽  
Bruno C. Alvarez ◽  
Angela Cubides ◽  
Angélica F. Luna ◽  
...  

2019 ◽  
Vol 12 (8) ◽  
pp. e229443 ◽  
Author(s):  
Caitlin Jane McNeill ◽  
Janev Fehmi ◽  
James Gladwin ◽  
Christopher Price

With the recent development of novel, more potent cancer treatment, in particular, immune ‘checkpoint inhibitors’, cases of neurological immune-related adverse events are on the rise. Although rare, this includes Guillain-Barré Syndrome (GBS). We present the case of a 68-year-old male who was admitted with sudden onset of worsening neurological symptoms following immunotherapy treatment. These symptoms progressed quickly to respiratory failure requiring intubation and admission to the intensive care unit. He was thoroughly investigated and is believed to have an axonal neuropathy in the form of Miller Fisher Syndrome (MFS) variant of GBS, secondary to immunotherapy treatment. He was initially treated with intravenous immunoglobulin, and later, perhaps more effectively, with high dose steroids which significantly improved his symptoms. This case of checkpoint inhibitor-induced MFS is one of few in the literature and is an important reminder of the potential for new immunotherapeutic agents to cause significant neurotoxic effects. These should be promptly and thoroughly investigated, in particular, as the management of these patients can differ from standard treatments used in these conditions.


2018 ◽  
Vol 129 (1) ◽  
pp. 127-132 ◽  
Author(s):  
Amandine Sevy ◽  
Aude-Marie Grapperon ◽  
Emmanuelle Salort Campana ◽  
Emilien Delmont ◽  
Shahram Attarian

2014 ◽  
Vol 125 ◽  
pp. S47-S48
Author(s):  
I. Khalil Ibrahim ◽  
M. Abdelhamid ◽  
M. Imam ◽  
N. Abdelmohsen ◽  
R. Awad

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