Dramatic resolution of disseminated pyoderma gangrenosum associated with monoclonal gammopathy after therapy with bortezomib and dexamethasone.

Pyoderma gangrenosum (PG) is an uncommon inflammatory and ulcerative skin disorder, which is commonly associated with systemic conditions such as inflammatory bowel disease, arthritis and haematological malignancies. It is widely stated that control of the underlying diseases may lead to resolution...

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Publicado en:International Wound Journal Vol. 14; no. 6; pp. 1382 - 1385
Autores principales: Velasco‐Tamariz, Virginia, Carreño‐Tarragona, Gonzalo, Tous‐Romero, Fátima, Gil‐de la Cruz, Elena, Martín‐Clavero, Estela, Rivera‐Díaz, Raquel
Formato: case study pictorial Journal Article
Publicado: Wiley-Blackwell Dec2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2017
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      pub: Wiley-Blackwell
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        atl: Dramatic resolution of disseminated pyoderma gangrenosum associated with monoclonal gammopathy after therapy with bortezomib and dexamethasone.
      aug:
        au:
          Velasco‐Tamariz, Virginia
          Carreño‐Tarragona, Gonzalo
          Tous‐Romero, Fátima
          Gil‐de la Cruz, Elena
          Martín‐Clavero, Estela
          Rivera‐Díaz, Raquel
        affil: Department of Dermatology, Hospital 12 de Octubre, Madrid Spain
      sug:
        subj:
          Pyoderma Gangrenosum
          Monoclonal Gammopathy of Undetermined Significance
          Bortezomib Therapeutic Use
          Dexamethasone Therapeutic Use
          Multiple Myeloma
          Sweet's Syndrome
          Female
          Adult
          Tumor Necrosis Factor
          Adult: 19-44 years
          Female
      ab: Pyoderma gangrenosum (PG) is an uncommon inflammatory and ulcerative skin disorder, which is commonly associated with systemic conditions such as inflammatory bowel disease, arthritis and haematological malignancies. It is widely stated that control of the underlying diseases may lead to resolution of PG. However, standard of care dictates that patients suffering with monoclonal gammopathy of undetermined significance or smouldering multiple myeloma (MM) should not receive therapy unless they progress to symptomatic MM. Here, we report a woman in her 40s with a disseminated corticodependent PG, resistant to any treatment attempted, including anti-tumoral necrosis factor (TNF) therapy in which bortezomib-dexamethasone regimen results in dramatic healing of all lesions in only a month. This case supports the belief that treatment of the underlying monoclonal gammopathy could be necessary when PG presents as an aggressive, non-responding skin disease.
      pubtype: Academic Journal
      doctype:
        case study
        pictorial
        Journal Article
      ougenre: Article
    language: English
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