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Spinal cord histopathological alterations in a patient with longstanding complex regional pain syndrome
Journal article   Peer reviewed

Spinal cord histopathological alterations in a patient with longstanding complex regional pain syndrome

Luis Del Valle, Robert J. Schwartzman and Guillermo Alexander
Brain, behavior, and immunity, v 23(1), pp 85-91
01 Jan 2009
PMID: 18786633

Abstract

Immunology Life Sciences & Biomedicine Neurosciences Neurosciences & Neurology Psychiatry Science & Technology
Complex regional pain syndrome (CRPS) is a chronic pain condition that usually arises from an injury or as a complication from a surgical procedure: CRPS can result from multiple mechanisms including active processes involving both the peripheral and the central nervous system and sickness like responses involving interactions between the immune and nervous systems. In animal models both peripheral and central sensitization as well as loss of inhibition has been implicated in neuropathic pain states. Glial cells, in particular microglia and astrocytes are the immunocompetent cells in the central nervous system and are activated following tissue injury or inflammation. In animal studies, activated glia have been shown to be both necessary and sufficient for enhanced nociception. Using immunohistochemical techniques, this study evaluated the degree of astrocytic and microglial activation as well as neuronal loss in autopsy tissue from the cervical, thoracic and lumbar spinal cord of a patient afflicted with CRPS as compared to four control individuals. The major findings of this study are that in long standing CRPS there was significant posterior horn cell loss and activation of both microglia and astrocytes most prominently at the level of the original injury but extending throughout the entire length of the spinal cord. Our hope is that the data obtained from this and other studies of autopsy material may aid in elucidating the mechanisms involved in the pathophysiology of CRPS, which may lead to the refinement of current therapies as well as novel treatments. (c) 2008 Elsevier Inc. All rights reserved

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Collaboration types
Domestic collaboration
Web of Science research areas
Immunology
Neurosciences
Psychiatry
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