Peristomal Pyoderma Gangrenosum Responding to Risankizumab.

Evidence to support available therapies for pyoderma gangrenosum (PG) is limited. Many patients do not respond to topical therapies such as tacrolimus or topical steroids. Currently favored oral systemic treatments (eg, cyclosporine and steroids) achieve complete remission in only 50% of patients an...

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Publicado en:Advances in Skin & Wound Care Vol. 34; no. 6; pp. 327 - 330
Autores principales: Weigelt, Maximillian A., Kirsner, Robert S.
Formato: case study pictorial Journal Article
Publicado: Lippincott Williams & Wilkins Jun2021
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2021
      vid: 34
      iid: 6
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      pub: Lippincott Williams & Wilkins
      place: Baltimore, Maryland
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        10.1097/01.ASW.0000744324.59877.df
        150384628
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        atl: Peristomal Pyoderma Gangrenosum Responding to Risankizumab.
      aug:
        au:
          Weigelt, Maximillian A.
          Kirsner, Robert S.
        affil: In Miami, Florida, Maximillian A. Weigelt, MD, is Clinical Research Fellow, Dr Phillip Frost Department of Dermatology & Cutaneous Surgery University of Miami Miller School of Medicine
      sug:
        subj:
          Ostomy Adverse Effects
          Pyoderma Gangrenosum Drug Therapy
          Antibodies, Monoclonal Therapeutic Use
          Dermatologic Agents Therapeutic Use
          Treatment Outcomes
          Female
          Adult
          Interleukins Antagonists and Inhibitors
          Biological Therapy
          Patient Safety
          Surgical Wound Infection Drug Therapy
          Adult: 19-44 years
          Female
      ab: Evidence to support available therapies for pyoderma gangrenosum (PG) is limited. Many patients do not respond to topical therapies such as tacrolimus or topical steroids. Currently favored oral systemic treatments (eg, cyclosporine and steroids) achieve complete remission in only 50% of patients and have unfavorable adverse effect profiles. There is a growing body of evidence to support biologic agents for the treatment of PG, but their exact role remains unclear. Here the authors present a patient with peristomal PG, the first reported case of PG responding to treatment with risankizumab, an anti-interleukin 23 monoclonal antibody. Risankizumab may represent an effective and relatively safe treatment for PG that merits additional exploration in prospective, controlled studies.
      pubtype: Academic Journal
      doctype:
        case study
        pictorial
        Journal Article
      ougenre: Article
    language: English
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