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Derm Pract ConceptObservational study

Mortality in Patients with Acquired Perforating Dermatosis

Results from the First Multicenter Case-Control Study.

Reyes-García S, Vázquez-López F, Galache-Osuna C, Vivanco-Allende B, González-Vela C, Santos-Juanes J, González-López MA

Dermatology Practical & ConceptualIn the feed 10 Oct 2026, published online 31 Jul 2026, issue 2026 Jul 31, added to PubMed 10 Oct 2026

Abstract

INTRODUCTIONMortality data in patients with acquired perforating dermatosis (APD) are limited.

OBJECTIVESTo assess, for the first time, the risk of all-cause mortality in adult patients with APD and to explore associated systemic comorbidities.

METHODSThis retrospective multicenter case-control study included adult patients diagnosed with APD and age-, sex-, and year-matched controls. We evaluated overall survival and the prevalence of seven major comorbidities: systemic malignancy, chronic obstructive pulmonary disease (COPD), severe liver disease, diabetes mellitus, arterial disease, hypertension, and dyslipidemia. Statistical analyses included univariate comparisons (Fisher's exact test and logistic regression), Kaplan-Meier survival estimates with log-rank tests, and multivariate Cox proportional hazards models.

RESULTSFifty-one patients with APD and 102 controls (1:2 ratio) were finally included in this investigation. Patients with APD had a significantly increased risk of mortality compared to controls ( log-rank test, P<0.001). In the multivariate Cox regression analysis, arterial disease emerged as the sole independent predictor of mortality (adjusted hazard ratio [HR]:7.716; 95% confidence interval [CI]: 2.774-21.464; P<0.001).

CONCLUSIONSThis is the first study to identify a potential association between APD and increased allcause mortality, primarily driven by coexisting arterial disease. These findings highlight the importance of comprehensive management in APD patients and emphasize the dermatologist's role in multidisciplinary care aimed at improving long-term outcomes.

Abstract from PubMed

PMID 42858395 · DOI 10.5826/dpc.1603a6672