Small Fiber Neuropathy: Clinicopathological Correlations.


Journal

Behavioural neurology
ISSN: 1875-8584
Titre abrégé: Behav Neurol
Pays: Netherlands
ID NLM: 8914585

Informations de publication

Date de publication:
2020
Historique:
received: 03 07 2019
revised: 13 10 2019
accepted: 26 11 2019
entrez: 14 5 2020
pubmed: 14 5 2020
medline: 26 1 2021
Statut: epublish

Résumé

Small fiber neuropathy develops due to the selective damage of the thin fibers of peripheral nerves. Many common diseases can cause this condition, including diabetes, infections, autoimmune and endocrine disorders, but it can occur due to genetic alterations, as well. Eighty-five skin biopsy-proven small-fiber neuropathy cases were analyzed. Forty-one (48%) cases were idiopathic; among secondary types, hypothyreosis (9.4%), diabetes mellitus (7%), cryoglobulinemia (7%), monoclonal gammopathy with unproved significance (4.7%), Sjögren's disease (3%), and paraneoplastic neuropathy (3%) were the most common causes. Two-thirds (68%) of the patients were female, and the secondary type started 8 years later than the idiopathic one. In a vast majority of the cases (85%), the distribution followed a length-dependent pattern. Intraepidermal fiber density was comparable in idiopathic and secondary forms. Of note, we found significantly more severe pathology in men and in diabetes. Weak correlation was found between patient-reported measures and pathology, as well as with neuropathic pain-related scores. Our study confirmed the significance of small fiber damage-caused neuropathic symptoms in many clinical conditions, the gender differences in clinical settings, and pathological alterations, as well as the presence of severe small fiber pathology in diabetes mellitus, one of the most common causes of peripheral neuropathy.

Identifiants

pubmed: 32399084
doi: 10.1155/2020/8796519
pmc: PMC7199601
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8796519

Informations de copyright

Copyright © 2020 Endre Pál et al.

Déclaration de conflit d'intérêts

The authors report no conflict of interest.

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Auteurs

Endre Pál (E)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
Department of Pathology, Neuropathology Unit, University of Pécs, Medical School, Pécs, Hungary.

Krisztina Fülöp (K)

Department of Pathology, Neuropathology Unit, University of Pécs, Medical School, Pécs, Hungary.

Péter Tóth (P)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.

Gabriella Deli (G)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.

Zoltán Pfund (Z)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.

József Janszky (J)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.

Sámuel Komoly (S)

Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.

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