key: cord-0844794-557j1oa0
authors: Randhawa, Jasneet; Randhawa, Harneet S; Toor, Prabhdeep
title: Pharyngeal-Cervical-Brachial Variant of Guillain-Barré Syndrome in a Patient of COVID-19 Infection
date: 2021-09-13
journal: Cureus
DOI: 10.7759/cureus.17945
sha: dadd572f73f090f3d2f9d58d81962d4f529dd911
doc_id: 844794
cord_uid: 557j1oa0

Guillain-Barré syndrome (GBS) has an annual incidence rate ranging from 0.4 to 1.7 cases per 1,00,000 population. Pharyngeal-cervical-brachial (PCB) variant is an extremely rare variant of GBS (3%), which presents with muscle weakness initially involving the neck, oropharynx, and upper extremities. GBS often has an infectious inciting event leading to an autoimmune response. There has been an increase in the incidence of GBS during the COVID-19 pandemic, and several case studies have shown an association between the development of GBS and COVID-19 infection. High clinical suspicion is needed to reach a diagnosis. As PCB variant of GBS can have fatal outcomes, a good clinical knowledge of its presentation can allow timely life-saving interventions. Here, we report a case of GBS with acute onset of neck and respiratory muscle weakness that progressed to upper limb weakness. The patient developed these symptoms two weeks after the onset of cough, fever, and malaise. PCB variant of GBS should always be considered as an important differential diagnosis in any patient presenting with limb weakness and bulbar palsy.

Guillain-Barré syndrome (GBS) is an acute progressive autoimmune polyradiculoneuropathy mostly involving the lower extremity motor nerves and ascending upward. GBS has an infectious preceding event leading to a hyperactive autoimmune response from the immune system against myelin coating of neurons predominantly in motor nerves. The pharyngeal-cervical-brachial (PCB) variant of GBS is interesting because of its unique presentation involving the neck, upper limb, and oropharyngeal muscles. It has a very low incidence and a significant risk of mortality due to the early involvement of respiratory muscles [1, 2] .

COVID-19 is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus. COVID-19 often presents with a sore throat, fever, and dry cough. Other complications from a prothrombotic state such as stroke, thromboembolism, etc. are also common in COVID-19 infection. GBS is one of the rare complications associated with COVID-19 infection, and not many cases of PCB variants have been reported [3] .

A 33-year-old male came to our emergency department with complaints of difficulty in breathing, upper limb weakness, dysphagia, and generalized weakness for two days. Two weeks before the onset of these symptoms, the patient had a cough and fever and was diagnosed with COVID-19 after the SARS-CoV-2 antigen test. Having mild symptoms and no other complications, the patient was advised of home isolation. SARS-CoV-2 antigen testing on admission was negative ( Figure 1 ). His vitals on admission were within normal limits. SpO2 was 89% on non-invasive ventilation (NIV). The patient was afebrile. On examination, single breath count (SBC) was 18, and power in upper limbs was decreased with absent deep tendon reflexes (DTR). Power in lower limbs was mildly decreased, and DTR was preserved ( MRI of the brain and cervical spine was done. No obvious abnormality or abnormal signal was noted in the brain or spinal cord. C6-C7 disk desiccation with mild bulge and no neural compromise was noted ( Figure 2 ). Thyroid function tests were within normal limits. Serum antinuclear antibody testing was negative. There was no loss of pain or temperature perception in extremities.

Clinical diagnosis of PCB variant of GBS was made, which was confirmed with the nerve conduction study ( Tables 2-4 ). Neurophysiological study of the peripheral nerves showed severe motor neuropathy of upper limbs along with reduced distal compound muscle action potential amplitudes in ulnar, median, tibial, and peroneal nerves bilaterally. Sensory parameters of the median, ulnar, and sural nerves were normal. The Fwaves study also confirmed peripheral motor neuropathy (Figures 3, 4) . The F-wave study is a pure motor test, which is similar to MNC and SNC. An electrode produces a supramaximal stimulus that travels backward into the anterior horn cells of the spinal cord and travels back into the motor nerve from there. This test is used to check the proximal segment of the nerve and helps to assess the causes of peripheral neuropathy [4] . 

After confirming the diagnosis with nerve conduction studies, intravenous immunoglobulin (IVIG) therapy was started. The patient's condition started to improve after 48 hours of treatment onset. As dyspnea improved, the patient was weaned off from NIV on the third day.

The patient was discharged with a prescription of Pregabalin and multivitamins and was advised regular physiotherapy. The patient had weak DTRs, and SBC was 44 on discharge ( 

We present a case of the PCB variant of GBS in a COVID-19-recovered patient. Several infections like Campylobacter jejuni, cytomegalovirus (CMV), diphtheria, HIV, etc. have been known to predispose a patient to GBS. Few cases of COVID-19 infection have also resulted in GBS according to recent case studies, and less than a handful have resulted in PCB variant.

Molecular mimicry is the proposed mechanism where the body's immune system makes antibodies against the infectious antigens, and these antibodies cross-react with normal body proteins and molecules leading to immune system activation and damaged body tissues. IgG (anti-GT1a) autoantibodies that react with the neuronal gangliosides are strongly positive in the PCB variant of GBS. These antibodies damage the peripheral nerves and cause a decrease in the conduction of nerve impulses. This causes motor neuropathy. The antibodies preferentially target the motor nerves compared to the sensory nerves and produce the characteristic syndrome [5] .

Several documented cases have shown an association between SARS-CoV-2 infection and GBS. Early intervention is needed in the PCB variant of GBS due to a higher risk of mortality compared to GBS. PCB variant of GBS and stroke can have a similar presentation. As there is an increased risk of hypercoagulability with COVID-19 infection, stroke is an important differential to be ruled out first for its effective and timely management. In our case, MRI helped to rule out stroke. The second common differential could be compression neuropathy. MRI of the cervical spine rules out compression neuropathy. Miller-Fisher syndrome (MFS) is a rare variant of GBS with a similar presentation, but lack of ophthalmoplegia which is a characteristic feature of MFS helped exclude this differential. Several endocrine disorders of the thyroid and adrenal glands are associated with peripheral neuropathies, but lack of suggestive symptoms for the same along with rapid development of symptoms in our patient and normal blood work helped rule out this differential diagnosis in our patient [6] [7] [8] .

GBS has a very rapid progression, and early intervention is always preferred to decrease the severity and to reduce the plateau duration of the disorder. There was an improvement in the administration of intravenous immunoglobulins suggesting a rather manageable form of the syndrome in our patient.

PCB variant of GBS has several differential diagnoses, and due to its rapid course and high fatality rate, a high clinical suspicion is needed in framing the diagnosis. Knowledge about how a case may present in a clinical setting is important for timely management. As statistical association does not imply causation, more epidemiological data and research are needed to exactly find how the SARS-CoV-2 virus aids in producing this syndrome and if any patient-specific trait increases its probability to cause GBS.

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

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