
Mucous membrane pemphigoid belongs to the family of sub-epidermal bullous diseases and is clinically characterized by mucosal involvement leading to fibrosis and scarring. Cutaneous involvement is unfrequent and oral mucosa and conjunctivas are the most frequently involves mucosa. Treatment relies on anti-inflammatory and immunosuppressive drugs. The main goal is the limitation of the fibrosing potential of the autoimmune deposits within various mucous membranes.
Tumor Necrosis Factor-alpha, Decision Trees, Pemphigoid, Benign Mucous Membrane, Anti-Inflammatory Agents, Antibodies, Monoclonal, Fluorescent Antibody Technique, Immunoglobulins, Intravenous, Enzyme-Linked Immunosorbent Assay, Mycophenolic Acid, Autoimmune Diseases, Diagnosis, Differential, Sulfasalazine, Antibodies, Monoclonal, Murine-Derived, Humans, France, Rituximab, Cyclophosphamide, Dapsone, Algorithms, Immunosuppressive Agents
Tumor Necrosis Factor-alpha, Decision Trees, Pemphigoid, Benign Mucous Membrane, Anti-Inflammatory Agents, Antibodies, Monoclonal, Fluorescent Antibody Technique, Immunoglobulins, Intravenous, Enzyme-Linked Immunosorbent Assay, Mycophenolic Acid, Autoimmune Diseases, Diagnosis, Differential, Sulfasalazine, Antibodies, Monoclonal, Murine-Derived, Humans, France, Rituximab, Cyclophosphamide, Dapsone, Algorithms, Immunosuppressive Agents
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