Chronic pain in pachyonychia congenita: evidence for neuropathic origin. (1st July 2018)
- Record Type:
- Journal Article
- Title:
- Chronic pain in pachyonychia congenita: evidence for neuropathic origin. (1st July 2018)
- Main Title:
- Chronic pain in pachyonychia congenita: evidence for neuropathic origin
- Authors:
- Brill, S.
Sprecher, E.
Smith, F.J.D.
Geva, N.
Gruener, H.
Nahman‐Averbuch, H.
Defrin, R. - Abstract:
- Summary: Background: Pachyonychia congenita (PC) is a rare autosomal dominant skin disease, with chronic pain being the most prominent complaint. Histological studies showing alterations in sensory innervation, along with reports on alterations in mechanical sensitivity, suggest that PC may be a form of neuropathy. Objectives: Here, for the first time, we aim to evaluate systematically the sensory function of patients with PC vs. controls, in order to investigate the pathophysiology of PC. Methods: Patients ( n = 62) and controls ( n = 45) completed the McGill and Douleur Neuropathique‐4 (DN4) questionnaires. Sensory testing included detection and pain thresholds, pathological sensations, conditioned pain modulation (CPM) and temporal summation of pain. Results: A moderate‐to‐severe chronic pain in the feet, throbbing and stabbing in quality, was highly prevalent among patients with PC (86%) and was especially debilitating during weight bearing. In addition, the majority of patients had a DN4 score ≥ 4 (62%), static allodynia (55%) and tingling (53%) in the feet. Compared with controls, patients with PC exhibited thermal and mechanical hypoaesthesia and mechanical hyperalgesia in the feet. CPM was reduced among the patients, and was associated with more enhanced mechanical hyperalgesia in the feet. The specific gene and nature of the causative mutation did not affect any of these features. Conclusions: Although thermal and mechanical hypoaesthesia may result from thickerSummary: Background: Pachyonychia congenita (PC) is a rare autosomal dominant skin disease, with chronic pain being the most prominent complaint. Histological studies showing alterations in sensory innervation, along with reports on alterations in mechanical sensitivity, suggest that PC may be a form of neuropathy. Objectives: Here, for the first time, we aim to evaluate systematically the sensory function of patients with PC vs. controls, in order to investigate the pathophysiology of PC. Methods: Patients ( n = 62) and controls ( n = 45) completed the McGill and Douleur Neuropathique‐4 (DN4) questionnaires. Sensory testing included detection and pain thresholds, pathological sensations, conditioned pain modulation (CPM) and temporal summation of pain. Results: A moderate‐to‐severe chronic pain in the feet, throbbing and stabbing in quality, was highly prevalent among patients with PC (86%) and was especially debilitating during weight bearing. In addition, the majority of patients had a DN4 score ≥ 4 (62%), static allodynia (55%) and tingling (53%) in the feet. Compared with controls, patients with PC exhibited thermal and mechanical hypoaesthesia and mechanical hyperalgesia in the feet. CPM was reduced among the patients, and was associated with more enhanced mechanical hyperalgesia in the feet. The specific gene and nature of the causative mutation did not affect any of these features. Conclusions: Although thermal and mechanical hypoaesthesia may result from thicker skin, its presentation in painful regions, along with mechanical hyperalgesia and allodynia, point towards the possibility of neuropathic changes occurring in PC. The clinical features and DN4 scores support this possibility and therefore neuropathic pain medications may be beneficial for patients with PC. … (more)
- Is Part Of:
- British journal of dermatology. Volume 179:Number 1(2018)
- Journal:
- British journal of dermatology
- Issue:
- Volume 179:Number 1(2018)
- Issue Display:
- Volume 179, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 179
- Issue:
- 1
- Issue Sort Value:
- 2018-0179-0001-0000
- Page Start:
- 154
- Page End:
- 162
- Publication Date:
- 2018-07-01
- Subjects:
- Dermatology -- Periodicals
Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2133 ↗
https://academic.oup.com/bjd ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjd.16217 ↗
- Languages:
- English
- ISSNs:
- 0007-0963
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24835.xml