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Co-occurrence of pemphigus vulgaris and multiple endocrine neoplasia type 1: a case report and review of literature

Emadodin Darchini-Maragheh; Sara Fakhraei; Pouran Layegh

Volume 25, Issue 2 , June 2022, , Pages 154-159

https://doi.org/10.22034/ijd.2021.248265.1215

Abstract
  Multiple endocrine neoplasia type 1 (MEN1) is a rare, autosomal dominant hereditary syndrome caused by mutations of the MEN1 tumor suppressor gene. We describe a patient with a prior confirmed diagnosis of pemphigus vulgaris (PV), who presented with new cutaneous manifestations that led to the diagnosis ...  Read More