Fatal paraneoplastic pemphigus associated with a mediastinal tumor |
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Authors: | Katharina Pfistershammer Gerald Minimair Dagmar Födinger Martin Czerny Christian Zauner Friederike Pieczkowski Georg Stingl Franz M. Karlhofer |
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Affiliation: | 1. Department of Dermatology, Division of Immunodermatology and Infectious Skin Diseases, Medical University of Vienna, Austria;2. Department of Dermatology, Division of General Dermatology, Medical University of Vienna, Austria;3. Department of Surgery, Medical University of Vienna, Austria;4. Department of Gastroenterology, AKH Vienna, Austria |
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Abstract: | Paraneoplastic pemphigus (PNP) is a rare life‐threatening autoimmune bullous skin disease which is an obligate paraneoplasma. A 34‐year‐old woman presented with recalcitrant stomatitis and a generalized lichenoid rash. A diagnosis of PNP was established based on clinical findings, immunofluorescence, histopathology and biochemistry. A localized mediastinal mass was found with CT imaging and excised. The histologic diagnosis was dendritic cell sarcoma. Despite removal of tumor and immunosuppressive therapy, the PNP progressed rapidly and the patient died of septic multiorgan failure. |
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Keywords: | paraneoplastic pemphigus immunoapheresis Castleman tumor |
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