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Muir‐Torre Syndrome
Author(s) -
Narita Hajime,
Kanzaki Tamotsu,
Yokota Michiko,
Matsuba Shozo
Publication year - 1992
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/j.1346-8138.1992.tb03189.x
Subject(s) - keratoacanthoma , medicine , dermatology , actinic keratosis , pathology , basal cell
Muir‐Torre syndrome is characterized by multiple sebaceous tumors, various internal malignancies and an autosomal dominant inheritance. We herein report a typical case. The patient was a 69‐year‐old man with sebaceous adenomas, a keratoacanthoma, and actinic keratosis in addition to carcinomas of the prostate, colon, duodenum, and larynx. His family members also suffered from multiple cancers.

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