Recurrent Guillain-Barré Syndrome – Case Series

Basta, Ivana; Božović, Ivo; Berisavac, Ivana; Stojiljkovic-Tamas, Olivera; Rajić, Sonja; Dominović-Kovačević, Aleksandra; Stojanov, Aleksandar; Djordjević, Gordana; Jovanović, Dejana; Perić, Stojan

doi:10.4103/0028-3886.273649

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2024

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Cited by 7 publications

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“…Recurrent GBS patients represent 6% of patients with GBS. 3 Miller Fisher syndrome is a variant of GBS. Recurrent Miller Fisher syndrome has been reported in children.…”

Section: To the Editorsmentioning

confidence: 99%

Recurrent GBS With COVID-19 in a Child: A Case Report

Akçay

Oğur

Menentoğlu

et al. 2022

Pediatric Infectious Disease Journal

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“…Recurrent GBS patients represent 6% of patients with GBS. 3 Miller Fisher syndrome is a variant of GBS. Recurrent Miller Fisher syndrome has been reported in children.…”

Section: To the Editorsmentioning

confidence: 99%

Recurrent GBS With COVID-19 in a Child: A Case Report

Akçay

Oğur

Menentoğlu

et al. 2022

Pediatric Infectious Disease Journal

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“…The treatment of this disease includes symptomatic support therapy, immunoglobulin therapy, plasma exchange therapy, and hormone therapy. The recurrence rate of GBS can be as high as 6%, and most studies showed a rate between 2% and 6.8%, [2,3] and this is called recurrent GBS. Recurrent patients have rapid symptom progression [4] and long onset time, they are difficult to be cured and show a slow recovery.…”

Section: Introductionmentioning

confidence: 99%

Radical radiotherapy for cervical cancer and meningioma with a history of Guillain-Barré syndrome: A case report

Deng

et al. 2022

Medicine

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Rationale: Guillain-Barré syndrome (GBS) is a rare autoimmune disease. Patients with cervical malignancies and intracranial meningiomas after the course of GBS are even rarer. There are no relevant reports at present. Patient concerns: We report a patient who developed cervical cancer (CC) and intracranial meningioma simultaneously after the course of GBS. Diagnoses: The history, pelvic enhanced magnetic resonance imaging (MRI) and pathology confirmed cervical squamous cell carcinoma, and the head enhanced MRI confirmed meningioma. Intervention: After multi-disciplinary team, the patient received head stereotactic radiosurgery for meningioma and radical radiotherapy for CC. Outcomes: The follow up for 1 year after treatment revealed a complete remission of the cervical tumor, stable disease of the meningioma, and no signs of GBS recurrence. Up to now, the general condition of the patient is acceptable and the curative effect is satisfactory. Lessons: This case report aims to improve the oncologists’ understanding of malignant tumors with rare autoimmune diseases and provide treatment reference for similar diseases in the future.

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