Identifier |
wh_ch61_p3529 |
Title |
Walsh & Hoyt: Pathogenesis and Pathophysiology |
Creator |
David I. Kaufman, DO |
Affiliation |
Chair, Neurology & Ophthalmology, Michigan State University |
Subject |
Demyelinating Diseases; Axonal Disorders; Acute Inflammatory Demyelinating Polyneuropathy; Pathogenesis; Pathophysiology |
Description |
The pathologic findings in AIDP are consistent with an acquired immune-mediated disorder. Clinical immunologic studies and findings in an almost identical animal model called experimental allergic neuritis indicate that both humoral and cell-mediated systems may participate in production of the disease. AIDP may be caused by antibodies to nerve tissue or soluble immune complexes. Macrophages seem to be the chief effector cells mediating damage to myelin, apparently acting as antigen-presenting cells. There also is evidence of activation of T-lymphocytes, but it is unclear if these cells have a primary pathogenic function or simply are involved secondarily in the inflammatory process. |
Date |
2005 |
Language |
eng |
Format |
application/pdf |
Type |
Text |
Source |
Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition |
Relation is Part of |
Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology |
Collection |
Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu |
Publisher |
Wolters Kluwer Health, Philadelphia |
Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
Rights Management |
Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
ARK |
ark:/87278/s6477k9w |
Setname |
ehsl_novel_whts |
ID |
185735 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6477k9w |