Oral pemphigus vulgaris: A case report with direct immunofluorescence study

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Oral pemphigus vulgaris: A case report with direct immunofluorescence study

Pemphigus vulgaris (PV) is a chronic, autoimmune, intraepidermal blistering disease of the skin and mucous membranes. The initial clinical manifestation is frequently the development of intraoral lesions, and later, the lesions involve the other mucous membranes and skin. The etiology of this disease still remains obscure although the presence of autoantibodies is consistent with an autoimmune ...

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Childhood pemphigus vulgaris: a case report

Pemphigus vulgaris (PV) is a potentially fatal autoimmune mucocutaneous blistering disease. Although PV occurs predominantly in adulthood, in the 3rd to 5th decades of life, there have rarely been reports of childhood cases which are often misdiagnosed. It presents as oral blisters that rupture rapidly and progress to painful erosions. Most patients develop cutaneous flaccid blisters that ruptu...

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Oral pemphigus vulgaris: a case report and literature update.

INTRODUCTION Pemphigus vulgaris is a rare cause of oral mucosal ulceration. CLINICAL PICTURE A 47-year-old Chinese man presented with a 3-month history of oral ulceration. There were no lesions on the skin or other mucosal sites. Histology and immunostaining were consistent with pemphigus vulgaris. TREATMENT Systemic and topical corticosteroids were instituted, together with topical antifun...

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A Case Report of Neonatal Pemphigus vulgaris

Pemphigus vulgaris (PV) is a chronic, rare mucocutaneous autoimmune bullous diseases characterized by flaccid blisters and/or pustules, with secondary erosions of the mucous membranes / skin. Pemphigus vulgaris is threatening patient life by the formation of splits within the epidermis, accompanied by acantholysis (separation of keratinocytes from each other). In this article, a term female neo...

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A Case of Pemphigus Vulgaris with Serum Autoantibodies Binding Blood Cell Antigen(s) on Immunofluorescence: A Case Report

Patients with pemphigus vulgaris (PV) may develop autoimmunity against an array of non-desmoglein antigens, including keratinocyte acetylcholine receptors. The latter, along with yet unknown autoantigens, could participate to PV pathogenesis. Here, we report a case of PV developing autoimmunity against peripheral blood mononuclear cell (PBMC) antigens. The patient was poorly responsive to stero...

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ژورنال

عنوان ژورنال: Journal of Oral and Maxillofacial Pathology

سال: 2016

ISSN: 0973-029X

DOI: 10.4103/0973-029x.190979