Juvenile pemphigus vulgaris: Literature review and a rare case report.

Autor:	Sriram, Shyamkumar, Hasan, Shamimul, Mansoori, Shahnaz, Saeed, Shazina, Banerjee, Abhishek, Ramalingam, Karthikeyan
Předmět:	PEMPHIGUS vulgaris LITERATURE reviews DELAYED diagnosis AUTOIMMUNE diseases MUCOUS membranes EPIDERMOLYSIS bullosa TISSUE adhesions
Zdroj:	Clinical Case Reports; May2024, Vol. 12 Issue 5, p1-15, 15p
Abstrakt:	Key Clinical Message: Pemphigus 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. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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