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  1. Article ; Online: Skin manifestations in tumor necrosis factor receptor-associated periodic syndrome (TRAPS).

    Schmaltz, Rebecca / Vogt, Thomas / Reichrath, Jörg

    Dermato-endocrinology

    2008  Volume 2, Issue 1, Page(s) 26–29

    Abstract: Tumor necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) is a rare autosomal ... about pathogenesis, clinical outcome and treatment options of skin manifestations in TRAPS. ... conjunctivitis. The histology of skin lesions in TRAPS is nonspecific, in general a perivascular dermal ...

    Abstract Tumor necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) is a rare autosomal dominant inherited disease that belongs to the group of hereditary fever syndromes, that are also named hereditary auto-inflammatory syndromes. TRAPS is characterized by a variety of naturally occurring mutations in a TNF receptor (TNFR), that affect the soluble TNFRSF1A gene in the 12p13 region. In some patients, the pathogenesis of TRAPS involves defective TNFRSF1A shedding from cell membranes in response to varying stimuli. TRAPS is characterized by the periodic occurrence of a broad variety of different clinical symptoms that represent an acute-phase response, including fever and pain in the joints, abdomen, muscles, skin or eyes, with broad variations across patients. In many cases, skin involvement is present that may include migratory patches, skin rashes, erysepela-like erythema, edematous plaques, urticaria, periorbital edema and/or conjunctivitis. The histology of skin lesions in TRAPS is nonspecific, in general a perivascular dermal infiltrate of lymphocytes and monocytes can be found. Cutaneous findings are of particular importance in TRAPS: they have been shown to give direction to the diagnosis of TRAPS and in most cases their treatment is challenging. As the incidence of TRAPS is very low, no prospective randomized controlled trials and only a few studies with case numbers up to twenty-five patients have been published. No guidelines for TRAPS treatment have been established so far. This review summarizes our present knowledge about pathogenesis, clinical outcome and treatment options of skin manifestations in TRAPS.
    Language English
    Publishing date 2008-05-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2540047-2
    ISSN 1938-1980 ; 1938-1980
    ISSN (online) 1938-1980
    ISSN 1938-1980
    DOI 10.4161/derm.2.1.12387
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Skin manifestations in autoinflammatory syndromes.

    Braun-Falco, Markus / Ruzicka, Thomas

    Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

    2011  Volume 9, Issue 3, Page(s) 232–246

    Abstract: ... in tumor necrosis factor receptor 1- or cryopyrin-associated periodic syndromes (TRAPS, CAPS), hyperimmunoglobulin D syndrome (HIDS ... of familial periodic fever syndromes of which familial Mediterranean fever (FMF) is the most common and best ... or Schnitzler syndrome; pyoderma gangrenosum and acne in PAPA syndrome; or behçetoid ...

    Abstract Autoinflammatory diseases encompass a group of inflammatory diseases that are non-infectious, non-allergic, non-autoimmune and non-immunodeficient. The term was initially coined for a small group of familial periodic fever syndromes of which familial Mediterranean fever (FMF) is the most common and best known. Genetic and molecular analyses demonstrated for the majority of these diseases an impairment of inflammasomes to cause an increased activity of an interleukin-1-dependent inflammatory response. Over the last years an increasing number of either rare hereditary syndromes or acquired common diseases could be summarized under the designation of autoinflammatory disease, thus creating an emerging new rubric of inflammatory diseases. Many of them display cutaneous manifestations as both concomitant or more rarely main symptoms. To name some of them like erysipelas-like erythema in FMF; urticaria-like rashes in tumor necrosis factor receptor 1- or cryopyrin-associated periodic syndromes (TRAPS, CAPS), hyperimmunoglobulin D syndrome (HIDS) or Schnitzler syndrome; pyoderma gangrenosum and acne in PAPA syndrome; or behçetoid aphthous ulcerations in HIDS and PFAPA syndrome. Based on the new insights into pathogenesis one increasingly realizes the good response of these diseases to IL-1 antagonist therapies.
    MeSH term(s) Hereditary Autoinflammatory Diseases/complications ; Hereditary Autoinflammatory Diseases/diagnosis ; Hereditary Autoinflammatory Diseases/therapy ; Humans ; Skin Diseases/diagnosis ; Skin Diseases/etiology ; Skin Diseases/therapy ; Syndrome
    Language German
    Publishing date 2011-03
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2093479-8
    ISSN 1610-0387 ; 1610-0379
    ISSN (online) 1610-0387
    ISSN 1610-0379
    DOI 10.1111/j.1610-0387.2010.07580.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Tumor necrosis factor receptor associated periodic fever syndrome with photographic evidence of various skin disease and unusual phenotypes: case report and literature review.

    Yao, Qingping / Englund, Kristin A / Hayden, Stephen P / Tomecki, Kenneth J

    Seminars in arthritis and rheumatism

    2012  Volume 41, Issue 4, Page(s) 611–617

    Abstract: Objectives: To report a case of tumor necrosis factor receptor associated periodic fever syndrome ... associated with gene mutations. Recognition of the unusual phenotypes may enhance early accurate diagnosis. ... with photographic evidence of various skin disease, including previously unreported vesicles and alopecia, as well ...

    Abstract 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.
    MeSH term(s) Female ; Fever ; Hereditary Autoinflammatory Diseases/diagnosis ; Hereditary Autoinflammatory Diseases/genetics ; Humans ; Middle Aged ; Receptors, Tumor Necrosis Factor, Type I/genetics
    Chemical Substances Receptors, Tumor Necrosis Factor, Type I
    Language English
    Publishing date 2012-02
    Publishing country United States
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 120247-9
    ISSN 1532-866X ; 0049-0172
    ISSN (online) 1532-866X
    ISSN 0049-0172
    DOI 10.1016/j.semarthrit.2011.07.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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