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Desquamative Gingivitis in the Context of Autoimmune Bullous Dermatoses and Lichen Planus-Challenges in the Diagnosis and Treatment

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DIAGNOSTICS
卷 12, 期 7, 页码 -

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MDPI
DOI: 10.3390/diagnostics12071754

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desquamative gingivitis; autoimmune bullous diseases; pemphigus vulgaris; bullous pemphigoid; cicatricial pemphigoid; lichen planus

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Desquamative gingivitis (DG) is a clinical term used to describe gingival erythema, desquamation, and erosions, with various underlying causes. Accurate diagnosis of the underlying disorder is crucial for appropriate treatment and prognosis. Patients typically seek dental consultation for DG, emphasizing the importance for dentists to be knowledgeable about this condition. Genetic predisposition, metabolic, neuropsychiatric, infectious factors, medication, among others, can lead to an inflammatory immune response in the oral mucosa and DG appearance. Comprehensive medical history, clinical examination, and relevant investigations are necessary for diagnosis. Management includes oral hygiene, regular follow-up, and systemic/topical therapy based on treatment algorithms.
Desquamative gingivitis (DG) is a clinical term that describes erythema, desquamation and erosions of the gingiva, of various etiologies. Although the clinical aspect is not specific for a certain disease, an accurate diagnosis of the underlying disorder is necessary because the disease course, prognosis and treatment vary according to the cause. DG may inflict significant oral discomfort, which is why patients typically present to the dentist for a first consultation, rendering it important for these specialists to be informed about this condition. Our paper aims to review the ethiopatogenesis and diagnostic approach of DG, focusing on the most common underlying disorders (autoimmune bullous dermatoses and lichen planus) and on the management of these patients. Potential etiological agents leading to an inflammatory immune response in the oral mucosa and DG appearance include genetic predisposition, metabolic, neuropsychiatric, infectious factors, medication, dental materials, graft-versus-host reaction and autoimmunity. A thorough anamnesis, a careful clinical examination, paraclinical explorations including histopathological exam and direct immunofluorescence are necessary to formulate an appropriate diagnosis. Proper and prompt management of these patients lead to a better prognosis and improved quality of life, and must include management in the dental office with sanitizing the oral cavity, instructing the patient for rigorous oral hygiene, periodic follow-up for bacterial plaque detection and removal, as well as topical and systemic therapy depending on the underlying disorder, based on treatment algorithms. A multidisciplinary approach for the diagnosis and follow-up of DG in the context of pemphigus vulgaris, bullous pemphigoid, cicatricial pemhigoid or lichen planus is necessary, including consultations with dermatologists, oral medicine specialists and dentists.

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