Tumor Necrosis Factor Receptor Associated Periodic Fever Syndrome with Photographic Evidence of Various Skin Disease and Unusual Phenotypes: Case Report and Literature Review
Autor: | Kristin Englund, Stephen P. Hayden, Qingping Yao, Kenneth J. Tomecki |
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Rok vydání: | 2012 |
Předmět: |
Fever
business.industry Hereditary Autoinflammatory Diseases Disease Middle Aged Gene mutation medicine.disease Proinflammatory cytokine Eastern european Pathogenesis Anesthesiology and Pain Medicine Rheumatology Receptors Tumor Necrosis Factor Type I Immunology medicine Atypia Humans Female Tumor necrosis factor alpha Periodic fever syndrome business |
Zdroj: | Seminars in Arthritis and Rheumatism. 41:611-617 |
ISSN: | 0049-0172 |
DOI: | 10.1016/j.semarthrit.2011.07.008 |
Popis: | Objectives To report a case of tumor necrosis factor receptor associated periodic fever syndrome (TRAPS) with unusual clinical phenotypes and a systematic review. Methods The relevant English literature of TRAPS was searched using the keywords TRAPS, autoinflammatory disease, and gene mutation. Original and review articles were reviewed and the clinical scenarios were exemplified with a case report. Results A 58-year-old Jewish woman with Eastern European Ashkenazic background presented with photographic evidence of various skin disease, including previously unreported vesicles and alopecia, as well as other systemic manifestations. The complaints of urinary foreign bodies prompted a discovery of ureteral strictures with atypia perhaps from autoinflammation. A R92Q gene mutation of TNFRSFA1 was detected. The clinical manifestations of this disease are protean and its pathogenesis is complex, involving the interaction of wild-type and mutated gene products, innate immune system, and proinflammatory cytokines. Glucocorticoid and anticytokine therapy is generally efficacious but some cases remain refractory to the current treatment. Conclusions TRAPS is a systemic autoinflammatory disease with variable clinical phenotypes associated with gene mutations. Recognition of the unusual phenotypes may enhance early accurate diagnosis. |
Databáze: | OpenAIRE |
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