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  4. Acute painful diabetic neuropathy: an uncommon, remittent type of acute distal small fibre neuropathy.
 
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Titre

Acute painful diabetic neuropathy: an uncommon, remittent type of acute distal small fibre neuropathy.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Swiss Medical Weekly  
Auteur(s)
Tran, C.
Auteure/Auteur
Philippe, J.
Auteure/Auteur
Ochsner, F.
Auteure/Auteur
Kuntzer, T.
Auteure/Auteur
Truffert, A.
Auteure/Auteur
Liens vers les personnes
Ochsner, François  
Kuntzer, Thierry  
Tran, Christel  
Liens vers les unités
Neurologie  
Recherche en neurosciences  
Endocrinologie diabétologie&métabo.  
Médecine génétique  
ISSN
1424-3997
Statut éditorial
Publié
Date de publication
2015
Volume
145
Première page
w14131
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article Publication Status: epublish
Résumé
INTRODUCTION: Acute painful diabetic neuropathy (APDN) is a distinctive diabetic polyneuropathy and consists of two subtypes: treatment-induced neuropathy (TIN) and diabetic neuropathic cachexia (DNC). The characteristics of APDN are (1.) the small-fibre involvement, (2.) occurrence paradoxically after short-term achievement of good glycaemia control, (3.) intense pain sensation and (4.) eventual recovery. In the face of current recommendations to achieve quickly glycaemic targets, it appears necessary to recognise and understand this neuropathy.
METHODS AND RESULTS: Over 2009 to 2012, we reported four cases of APDN. Four patients (three males and one female) were identified and had a mean age at onset of TIN of 47.7 years (±6.99 years). Mean baseline HbA1c was 14.2% (±1.42) and 7.0% (±3.60) after treatment. Mean estimated time to correct HbA1c was 4.5 months (±3.82 months). Three patients presented with a mean time to symptom resolution of 12.7 months (±1.15 months). One patient had an initial normal electroneuromyogram (ENMG) despite the presence of neuropathic symptoms, and a second abnormal ENMG showing axonal and myelin neuropathy. One patient had a peroneal nerve biopsy showing loss of large myelinated fibres as well as unmyelinated fibres, and signs of microangiopathy.
CONCLUSIONS: According to the current recommendations of promptly achieving glycaemic targets, it appears necessary to recognise and understand this neuropathy. Based on our observations and data from the literature we propose an algorithmic approach for differential diagnosis and therapeutic management of APDN patients.
PID Serval
serval:BIB_D7566BA100A9
DOI
10.4414/smw.2015.14131
PMID
25941879
WOS
000355007900001
Permalien
https://iris.unil.ch/handle/iris/230117
Open Access
Oui
Date de création
2015-06-12T15:39:13.320Z
Date de création dans IRIS
2025-05-21T05:04:55Z
Fichier(s)
En cours de chargement...
Vignette d'image
Nom

25941879.pdf

Version du manuscrit

published

Taille

848.17 KB

Format

Adobe PDF

PID Serval

serval:BIB_D7566BA100A9.P001

URN

urn:nbn:ch:serval-BIB_D7566BA100A96

Somme de contrôle

(MD5):70881d88494db71efa2f7dd3a97f48cc

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