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Mortality and Autopsy Findings in Patients with Pyoderma Gangrenosum: A Multi-Institutional Series.
Shakshouk, Hadir; deCampos-Stairiker, Mallory; Kody, Shannon; Stenzel, Peter; Xia, Eric; Mostaghimi, Arash; Wu, Bicong; Shinohara, Michi M; Marzano, Angelo V; Polly, Samantha; Fernandez, Anthony P; Ortega-Loayza, Alex G.
Affiliation
  • Shakshouk H; Department of Dermatology, Oregon Health and Science University, Portland, Oregon, USA.
  • deCampos-Stairiker M; Oregon Health and Science University School of Medicine, Portland, Oregon, USA.
  • Kody S; Department of Dermatology, Oregon Health and Science University, Portland, Oregon, USA.
  • Stenzel P; Department of Pathology, Oregon Health and Science University, Portland, Oregon, USA.
  • Xia E; Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Mostaghimi A; Boston University School of Medicine, Boston, Massachusetts, USA.
  • Wu B; Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Shinohara MM; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Marzano AV; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Polly S; Division of Dermatology, University of Washington, Seattle, Washington, USA.
  • Fernandez AP; Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Ortega-Loayza AG; Department of Pathophysiology and Transplantation, Università Degli Studi di Milano, Milan, Italy.
Dermatology ; 240(2): 352-356, 2024.
Article in En | MEDLINE | ID: mdl-38185115
ABSTRACT

INTRODUCTION:

Pyoderma gangrenosum (PG) is a rare ulcerative skin condition with an increased risk of mortality compared to the general population. The causes of this increased risk are not well understood. Misdiagnosis is common in PG, and many studies are limited by the inclusion of misdiagnosed cases. The goal of this study was to review autopsy findings, identify causes of death, and identify factors that may worsen outcomes among deceased patients confirmed to have PG.

METHODS:

Data was retrospectively reviewed from the electronic medical records at five academic hospitals. A search was conducted for deceased patients with a diagnosis of PG who had an autopsy performed between 2010 and 2020. We report a descriptive analysis of 11 patients and their clinical characteristics, causes of death, and autopsy findings.

RESULTS:

The average age of death was 62.9 years. Seven patients had at least one underlying condition known to be associated with PG including inflammatory bowel disease, inflammatory arthritis, or a hematologic disorder. The most common cause of death was infection (n = 6, 54.5%), followed by pulmonary embolism (n = 3, 27.3%), and myelodysplastic syndrome (n = 2, 18.2%). Six patients (54.5%) were taking systemic steroids at the time of death.

CONCLUSION:

The development of PG may shorten life expectancy among those with underlying conditions associated with PG, and common treatments for PG may contribute to the risk of fatal complications. Awareness of the risk of infection, thrombosis, and malignancy among those with PG is necessary for proper management. Further research is needed to explore the relationship between PG and thromboembolism.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Ulcer / Inflammatory Bowel Diseases / Pyoderma Gangrenosum Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Middle aged Language: En Journal: Dermatology Journal subject: DERMATOLOGIA Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Ulcer / Inflammatory Bowel Diseases / Pyoderma Gangrenosum Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Middle aged Language: En Journal: Dermatology Journal subject: DERMATOLOGIA Year: 2024 Document type: Article Affiliation country: United States