Juvenile pemphigus vulgaris: Literature review and a rare case report

Author:

Sriram Shyamkumar1,Hasan Shamimul2ORCID,Mansoori Shahnaz2,Saeed Shazina3ORCID,Banerjee Abhishek4,Ramalingam Karthikeyan5ORCID

Affiliation:

1. Department of Social and Public Health Ohio University Athens Ohio USA

2. Department of Oral Medicine and Radiology Faculty of Dentistry, Jamia Millia Islamia New Delhi India

3. Amity Institute of Public Health & Hospital Administration Amity University Noida Uttar Pradesh India

4. Oral and Maxillofacial Pathology Awadh Dental College and Hospital Jamshedpur Jharkhand India

5. Department of Oral Pathology and Microbiology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences Saveetha University Chennai India

Abstract

Key Clinical MessagePemphigus vulgaris (PV) is a chronic autoimmune blistering disorder characterized by the loss of intraepithelial adhesion affecting the skin and mucous membranes, predominantly affects females in their fifth and sixth decades of life. Due to its rare occurrence in children and adolescents, there is often a delay in diagnosis and treatment in this age group. PV should always be considered in the differential diagnosis of oral ulcerative and vesiculobullous lesions in both children and adolescents.

Publisher

Wiley

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