Immune Dysregulation,Polyendocrinopathy, Enteropathy,X‐Linked Syndrome Associated with Neonatal Epidermolysis Bullosa Acquisita |
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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 |
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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 |
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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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