Wells’ Syndrome Associated with Churg-Strauss Syndrome
2
조회
0
다운로드
2
인용
0
참고문헌
키워드
초록
Churg-Strauss syndrome (CSS) is a multisystem granulomatous vasculitis that is characterized by peripheral eosinophilia and the infiltration of eosinophils into systemic organs. The skin lesions of CSS consist mainly of palpable purpura and nodules. Wells' syndrome (WS) is a rare inflammatory dermatosis that is associated with recurrent granulomatous dermatitis and eosinophilia. Since these two diseases are rare, any overlap between them is very unusual. Herein, we report a patient with CSS, who initially presented a skin eruption of erythematous urticarial-plaques,vesicles, and blisters. Upon biopsy, the histology of these plaques indicated eosinophilic infiltration and “flame figures“ within the dermis, which was consistent with a diagnosis of WS. Although the association between WS and CSS that was observed in our patient may be purely coincidental, it could also suggest a common pathogenetic background of these two distinct diseases, as both share several many common features. (Ann Dermatol 23(4) 497∼500, 2011)
Abstract
Churg-Strauss syndrome (CSS) is a multisystem granulomatous vasculitis that is characterized by peripheral eosinophilia and the infiltration of eosinophils into systemic organs. The skin lesions of CSS consist mainly of palpable purpura and nodules. Wells' syndrome (WS) is a rare inflammatory dermatosis that is associated with recurrent granulomatous dermatitis and eosinophilia. Since these two diseases are rare, any overlap between them is very unusual. Herein, we report a patient with CSS, who initially presented a skin eruption of erythematous urticarial-plaques,vesicles, and blisters. Upon biopsy, the histology of these plaques indicated eosinophilic infiltration and “flame figures“ within the dermis, which was consistent with a diagnosis of WS. Although the association between WS and CSS that was observed in our patient may be purely coincidental, it could also suggest a common pathogenetic background of these two distinct diseases, as both share several many common features. (Ann Dermatol 23(4) 497∼500, 2011)
참고문헌 (11)
- Wells GC, "Eosinophilic cellulitis", Br J Dermatol, 100, pp.101~109 (1979)
- Schuttelaar ML, "Bullous eosinophilic cellulitis (Wells' syndrome) associated with Churg-Strauss syndrome", J Eur Acad Dermatol Venereol, 17, pp.91~93 (2003)
- Lee SC, "Wells syndrome associated with Churg-Strauss syndrome", J Am Acad Dermatol, 43, pp.556~557 (2000)
- Govoni M, "Churg-Strauss syndrome and Wells syndrome: coincidence or pathogenetic association? A new case report", Clin Exp Rheumatol, 25(1), pp.41~ (2007)
- Fujimoto N, "Wells syndrome associated with Churg-Strauss syndrome", Clin Exp Dermatol, 36, pp.46~48 (2011)
- Masi AT, "The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis)", Arthritis Rheum, 33, pp.1094~1100 (1990)
- Katoulis AC, "Idiopathic bullous eosinophilic cellulitis (Wells' syndrome)", Clin Exp Dermatol, 34, pp.375~376 (2009)
- Caputo R, "Wells syndrome in adults and children: a report of 19 cases", Arch Dermatol, 142, pp.1157~1161 (2006)
- Gilliam AE, "Bullous "cellulitis" with eosinophilia: case report and review of Wells' syndrome in childhood", Pediatrics, 116, pp.149~155 (2005)
- Churg J, "Allergic granulomatosis, allergic angiitis, and periarteritis nodosa", Am J Pathol, 27, pp.277~301 (1951)
- Kallenberg CG, "Churg-Strauss syndrome: just one disease entity", Arthritis Rheum, 52, pp.2589~2593 (2005)
