Paraneoplastic autoimmune multiorgan syndrome (PAMS)

Abstract
Originally described by Anhalt as paraneoplastic pemphigus in 1990, paraneoplastic autoimmune multiorgan syndrome (PAMS) is a potentially lethal blistering disease, characterized by polymorphous clinical features, including mucocutaneous erosions, blisters, lichenoid papules, and erythema. Several autoantibodies have been detected in serum of PAMS patients, including anti-plakins, anti-alpha-2-macroglobulin like 1, and anti-desmogleins...
Paper Details
Title
Paraneoplastic autoimmune multiorgan syndrome (PAMS)
Published Date
May 1, 2021
Volume
156
Issue
2
Pages
174 - 183
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