Abstract
This case report is mainly about the rare auto immune disease pemphigus vulgaris. Its onset appears on the basis of interaction between genetic predisposition and various triggering factors. Mostly it is clinical presented as oral lesions, mucosal lesions, skin blisters that are itchy and painful. It affects people around the age of 50 to 60 mostly Jewish heritages from southeast Europe, India and the Middle East. Basing on clinical features, histopathological and immunopathological findings it has to diagnose and must be treated immediately because, delayed treatment cannot be helpful and may cause fatality to the patient.
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