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- W2153102759 abstract "Keratoacanthoma (KA) is an extraordinary entity. Once considered a benign neoplasm that resembled a highly malignant one (pseudomalignancy), it is now viewed in an opposite light as a cancer that resembles a benign neoplasm (pseudobenignity).The goal was to delineate the malignant potential of this neoplasm based on the author's experience and a review of recent data and research and to emphasize the KA as a possible part of an autosomal dominant familial cancer syndrome, the Muir-Torre syndrome.This is a review of the literature.In this work, the KA is reviewed with recent advances emphasized.KA is an abortive malignancy that rarely progresses into an invasive SCC. The KA may serve as a marker for the important autosomal dominant familial cancer syndrome, the Muir-Torre syndrome, as a result of a defective DNA mismatch repair gene." @default.
- W2153102759 created "2016-06-24" @default.
- W2153102759 creator A5073881883 @default.
- W2153102759 date "2004-02-01" @default.
- W2153102759 modified "2023-10-18" @default.
- W2153102759 title "Keratoacanthoma: A Clinico-Pathologic Enigma" @default.
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- W2153102759 doi "https://doi.org/10.1111/j.1524-4725.2004.30080.x" @default.
- W2153102759 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14871228" @default.
- W2153102759 hasPublicationYear "2004" @default.
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