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Immune Dysregulation,Polyendocrinopathy, Enteropathy,X‐Linked Syndrome Associated with Neonatal Epidermolysis Bullosa Acquisita
Authors:Sabina Bis MD  Sheilagh M Maguiness MD  Stephen E Gellis MD  Lynda C Schneider MD  Pui Y Lee MD  Luigi D Notarangelo MD  Sevgi Keles MD  Talal A Chatila MD  Birgitta A Schmidt MD  Daniel D Miller MD
Institution:1. Harvard Combined Dermatology Program, Boston, Massachusetts;2. Division of Immunology, Department of Medicine, Boston Children's Hospital, Boston, Massachusetts;3. Department of Dermatology, School of Medicine, Boston University, Boston, Massachusetts
Abstract:We report the case of a 2‐week‐old boy who presented with a vesiculopustular, bullous eruption in the setting of autoimmune enteropathy, hypothyroidism, membranous nephropathy, Coombs‐positive hemolytic anemia, and persistent eosinophilia. Immunologic testing revealed a deficiency of FOXP3‐expressing regulatory T cells, and a diagnosis of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome was made. Histologic analysis, immunofluorescence, and enzyme‐linked immunosorbent assay confirmed the bullous eruption as epidermolysis bullosa acquisita with associated collagen VII autoantibody production. The skin lesions responded to systemic immunosuppressant therapy and have regressed after allogeneic bone marrow transplantation.
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