Muir-Torre syndrome: a variant of the cancer family syndrome.

Abstract

Muir-Torre syndrome is characterised by the association of sebaceous tumours of the skin with internal malignancy. In many instances there is a strong family history of cancer and the autosomal dominant mode of inheritance, tumour spectrum, and high incidence of synchronous and metachronous tumours show parallels with the cancer family syndrome or Lynch II syndrome. We report a five generation family with at least two persons displaying the Muir-Torre phenotype, while many other family members have had tumours consistent with cancer family syndrome. The majority of tumours are gastrointestinal, gynaecological, and urological, with several persons having multiple primaries. The prognosis appears to be better than would be expected. Sebaceous tumours are a marker for internal malignancy and should prompt a search for occult cancer in the individual person and family members. In documented Muir-Torre families, at risk persons should be entered into screening programmes similar to those used in the Lynch II syndrome.

• Authors: N R Hall, M A Williams, V A Murday, J A Newton, D T Bishop
• Journal: Journal of medical genetics (J Med Genet) Vol. 31 Issue 8 Pg. 627-31 (Aug 1994) ISSN: 0022-2593 [Print] England
• PMID: 7815421 (Publication Type: Journal Article)

Topics

• Adult
• Aged
• Colorectal Neoplasms (genetics)
• Female
• Humans
• Male
• Middle Aged
• Neoplasms, Multiple Primary (genetics)
• Neoplasms, Second Primary (genetics)
• Neoplasms, Unknown Primary (diagnosis, genetics)
• Neoplastic Syndromes, Hereditary (genetics)
• Pedigree
• Prognosis
• Sebaceous Gland Neoplasms (genetics)