Small Fiber Neuropathy Associated with Post-COVID-19 and Post-COVID-19 Vaccination Arthritis: A Rare Post-Infective Syndrome or a New-Onset Disease?

Author:

Bandinelli Francesca1ORCID,Nassini Romina23ORCID,Gherardi Eleonora4,Chiocchetti Barbara5,Manetti Mirko6ORCID,Cincotta Massimo5,Nozzoli Filippo7,Nucci Elena8,De Logu Francesco2,Pimpinelli Nicola4

Affiliation:

1. Rheumatology Department, San Giovanni di Dio Hospital, Usl Tuscany Center, 50143 Florence, Italy

2. Section of Clinical Pharmacology and Oncology, Department of Health Sciences, University of Florence, 50139 Florence, Italy

3. Headache Center and Clinical Pharmacology Unit, Careggi University Hospital, 50139 Florence, Italy

4. Section of Dermatology, Department of Health Sciences, University of Florence, 50125 Florence, Italy

5. Neurology Department, San Giovanni di Dio Hospital, Usl Tuscany Center, 50143 Florence, Italy

6. Section of Anatomy and Histology, Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy

7. Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy

8. Histopathology and Molecular Diagnostics Unit, Careggi University Hospital, University of Florence, 50139 Florence, Italy

Abstract

Post-COVID-19 (PC) and post-COVID-19 vaccination (PCV) syndromes are considered emergent multidisciplinary disorders. PC/PCV small fiber neuropathy (SFN) was rarely described and its association with undifferentiated arthritis (UA) was never defined. We aimed to evaluate PC/PCV-UA associated with the recent onset of severe lower limb paresthesia, compare SFN positive (+) to negative (−) patients, and evaluate changes in biomarkers in SFN+ during treatments. Nineteen PC/PCV-UA-patients with possible SFN underwent skin biopsy at the Usl Tuscany Center (Florence) early arthritis outpatient clinic from September 2021 to March 2024. Eight selected SFN+ were compared to ten SFN− patients. In SFN+ patients, baseline joint ultrasound (US), electromyography (EMG), optical coherence tomography (OCT), and skin biopsy were repeated at six months. Moreover, SFN+ patients were clinically assessed by a 0–10 numeric rating scale for neurological symptoms and DAS28/ESR up to 12 months follow-up. SFN+ patients showed a lower intraepidermal nerve fiber density at histopathological examination of skin biopsies and a higher frequency of OCT and EMG abnormalities in comparison to SFN− patients. In SFN+ patients, US and DAS28/ESR significantly improved, while intraepidermal nerve fiber density did not significantly change at the six-month follow-up. Fatigue, motor impairment, burning pain, brain fog, and sensitivity disorders decreased at long-term follow-up (12 months).

Publisher

MDPI AG

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