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Paget disease of the vulva

Authors :
J.A. de Hullu
K.A.P. Meeuwis
M.I.E. van Poelgeest
M. van der Linden
Tjalling Bosse
Johan Bulten
Source :
Critical Reviews in Oncology Hematology, 101, 60-74, Critical Reviews in Oncology Hematology, 101, pp. 60-74, Critical Reviews in Oncology/Hematology, 101, 60-74
Publication Year :
2016

Abstract

Contains fulltext : 171122.pdf (Publisher’s version ) (Open Access) In this review, we provide an overview of the clinical aspects, histopathology, molecular genetics, and treatment options for Vulvar Paget's Disease (VPD), a rare skin disease, most commonly found in postmenopausal Caucasian women. The underlying cause of VPD remains not well understood. VPD is rarely associated with an underlying urogenital, gastrointestinal or vulvar carcinoma. In approximately 25% of the cases, VPD is invasive; in these cases, the prognosis is worse than in non-invasive cases. Recurrence rates in invasive VPD are high: 33% in cases with clear margins, and even higher when surgical margins are not clear, regardless of invasion. Historically, surgical excision has been the treatment of choice. Recent studies show that imiquimod cream may be an effective and safe alternative.

Details

Language :
English
ISSN :
10408428
Database :
OpenAIRE
Journal :
Critical Reviews in Oncology Hematology, 101, 60-74, Critical Reviews in Oncology Hematology, 101, pp. 60-74, Critical Reviews in Oncology/Hematology, 101, 60-74
Accession number :
edsair.doi.dedup.....00e4f51f4c07ba2984d17f61bb15be97