Celulitis eosinofílica (síndrome de Wells)A propósito de un caso

  1. Daniel Corrales Cruz 1
  2. Maximiliano Rodrigo Gómez de la Bárcena 1
  3. Isabel García Higuera 1
  4. Isabel Viqueira Rodriguez 1
  5. María José Cáceres Porras 1
  6. Estibaliz Obregón Martínez 1
  7. Esther Riñones Mena 1
  8. Enrique García Toro 1
  1. 1 Complejo Asistencial Universitario de Burgos
    info

    Complejo Asistencial Universitario de Burgos

    Burgos, España

    ROR https://ror.org/01j5v0d02

Revue:
Revista Electrónica de Biomedicina

ISSN: 1697-090X

Année de publication: 2014

Número: 1

Pages: 33-37

Type: Article

D'autres publications dans: Revista Electrónica de Biomedicina

Résumé

The "Wells syndrome" is a rare inflammatory dermatosis of unknown pathogenesis, clinical polymorph, both the location and the extent of the lesions. This is a skin disease of inflammatory origin, which usually appears in children and adolescents. Has a polymorphic clinical picture, both the location and the extent of the lesions, and for the correct interpretation of diagnostic histopathological lesions required. This entity should be considered in the differential diagnosis of any atypical presentation of cellulite with peripheral eosinophilia, that does not respond to antibiotics.

Références bibliographiques

  • Wells GC. Recurrent granulomatous dermatitis with eosinophilia. Trans St Johns Hosp Dermatol Soc. 1971;57:46–56
  • Spigel GT, Winkelmann RK. Wells' syndrome: recurrent granulomatous dermatitis with eosinophilia. Arch Dermatol. 1979;115(5):611-613.
  • Blanco MB, Pereira C, Chieira C, Rodríguez MA. Síndrome de Wells. A propósito de dos casos. Alergol Inmunol Clin 2002; 17: 108-110.
  • González Martínez F, Santos Sebástián MM, Navarro Gómez ML, Saavedra Lozano J, Hernández Sampelayo T. Celulitis eosinofílica: síndrome de Wells. An Pediat 2009;70:508-510
  • Gilliam AE, Bruckner AL, Howard RM, Lee BP, Wu S, Frieden IJ. Bullous "cellulitis" with eosinophilia: Case report and review of Wells' syndrome in childhood. Pediatrics. 2005;116:e149-155.
  • Sinno H, Lacroix JP, Lee J, Izadpanah A, Borsuk R, Watters K, Gilardino M. Diagnosis and management of eosinophilic cellulitis (Wells' syndrome): A case series and literature review. Can J Plast Surg. 2012;20:91-97.
  • Haddad F, Helm TN. Wells syndrome. Cutis. 2014;93(1):17, 38-39.
  • Bansal M, Rai T, Pandey SS. Wells syndrome. Indian Dermatol Online J. 2012;3(3):187-189.
  • Powell J, Salim A, Muc R, Colloby P, Kaur MR. Persistent hypereosinophilia with Wells syndrome. Clin Exp Dermatol. 2013;38(1):40-43.
  • Rongioletti F, Fausti V, Kempf W, Rebora A, Parodi A. Eosinophilic annular erythema: an expression of the clinical and pathological polymorphism of Wells syndrome. J Am Acad Dermatol. 2011;65(4):e135-137.
  • Brehmer-Andersson E, Kaaman T, Skog E, Frithz A. The histopathogenesis of the flame figure in Wells' syndrome based on five cases. Acta Derm Venereol. 1986;66(3):213-219.
  • Heelan K, Ryan JF, Shear NH, Egan CA. Wells syndrome (eosinophilic cellulitis): Proposed diagnostic criteria and a literature review of the drug-induced variant. J Dermatol Case Rep. 2013;7(4):113-120.