Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/57956
Title: Paraneoplastic pityriasis rubra pilaris: a systematic review.
Authors: Gaston J.;Lee S.;Lai F.Y.X.;Maxwell A.
Monash Health Department(s): Dermatology
Institution: (Gaston) Department of Dermatology, The Royal Children's Hospital Melbourne, Melbourne, VIC, Australia

(Maxwell) Department of Dermatology, Royal Melbourne Hospital, Melbourne, VIC, Australia

(Lai, Lee) Department of Dermatology, Monash Health, Clayton, VIC, Australia

(Lai, Lee) Skin Health Institute, Carlton, VIC, Australia

(Lee) Department of Dermatology, Eastern Health, Box Hill, VIC, Australia

(Lee) Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia
Issue Date: 17-Mar-2026
Copyright year: 2026
Publisher: Oxford University Press
Place of publication: United Kingdom
Publication information: Clinical and Experimental Dermatology. 51(3) (pp 374-380), 2026. Date of Publication: 01 Mar 2026.
Journal: Clinical and Experimental Dermatology
Abstract: Background Paraneoplastic pityriasis rubra pilaris (PRP) is a rare and poorly defined chronic inflammatory skin condition. Recognition of its potential association with cancer is crucial to facilitate timely diagnosis and treatment. Objectives To summarize published literature on paraneoplastic PRP, with a focus on associated cancer types, latency periods, treatment outcomes and resolution following oncological management. Methods A literature review was conducted following PRISMA guidelines using the MEDLINE, Embase, Cochrane Library and Web of Science databases. Search terms used were 'pityriasis rubra pilaris', 'malignancy', 'cancer' and 'paraneoplastic', and inclusion criteria were adults diagnosed with both cancer and probable paraneoplastic PRP. Two authors independently reviewed the titles and abstracts of all identified papers before the full text of potentially relevant studies was retrieved for further analysis. Results From 978 articles screened, 22 studies describing 23 adult patients were included. Solid tumours were implicated in 83% of cases (n = 19/23), with lung cancer the most common of these (n = 7/19, 37%). The median latency from PRP onset to cancer diagnosis was 9 weeks [interquartile range (IQR): 0.4-25.0]. Among 17 patients experiencing complete or partial resolution of PRP following treatment for their cancer, complete resolution occurred in 65% (n = 11/17), typically within a median of 11 weeks (IQR: 6.8-22.8). The overall mortality rate in evaluable cases was 16% (n = 3/19). Conclusions In this systematic review, paraneoplastic PRP was associated with multiple types of cancer, both solid and haematological. Cancer screening should be considered in cases of atypical or treatment-refractory PRP. Further prospective studies are required to define predictive features and optimize diagnostic approaches.Copyright © The Author(s) 2025. Published by Oxford University Press on behalf of British Association of Dermatologists. All rights reserved.
DOI: https://dx.doi.org/10.1093/ced/llaf472
PubMed URL: 41134711
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/57956
Type: Review
Appears in Collections:Articles

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