Results 71 to 80 of about 1,372,625 (169)

Ileocecal Adenocarcinoma and Ureteral Transitional Cell Carcinoma with Multiple Sebaceous Tumors and Keratoacanthomas in a Case of Muir-Torre Syndrome

Dermatology Research and Practice, 2010
Cutaneous neoplasms including sebaceous tumors, keratoacanthomas, and basal cell carcinomas with sebaceous differentiation can be markers of internal malignancy associated with the Muir-Torre Syndrome (MTS).
Michael C. Lynch, Bryan E. Anderson
doaj   +1 more source

Dermatopathologic emergencies part I

Indian Journal of Dermatopathology and Diagnostic Dermatology, 2017
In dermatopathology, there are several conditions which must be addressed emergently. While some conditions necessitate emergent intervention because of the pathology of the cutaneous manifestations, others require recognition of the underlying serious ...
Douglas Hoffman Atmatzidis, Karl Hoegler, Amy R Weiss, W Clark Lambert   +3 more
doaj   +1 more source

A Case of Muir-Torre Syndrome

, 2004
Muir-Torre syndrome(MTS) is an autosomal dominant genodermatosis first described in 1967 by Muir and in 1968 by Torre. It is characterized by the presence of at least one sebaceous gland tumor and the presence of a low-grade internal malignancy.
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core  

Sebaceous carcinoma of the skin of the breast: a case report

Journal of Medical Case Reports, 2008
Introduction Sebaceous gland tumours are rare and their presence should be considered as a marker for Muir-Torre Syndrome, alerting to search for an occult malignancy.
Alzaraa Ahmed, Ghafoor Imran, Yates Andrew, Dhebri Alhad   +3 more
doaj   +1 more source

Sebaceous carcinoma over cheek: A rare presentation

Medical Journal of Dr. D.Y. Patil University, 2014
Sebaceous carcinoma, an uncommon cutaneous tumor first described by Allaire in 1891. This arises mostly from sebaceous glands in the skin and thus may arise anywhere in the body where these glands exist.
Dakshayani S Nirhale, Amit Parasnis, Virendra S Athavale, Mohit Bhatia   +3 more
doaj   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Neue S1‐Leitlinie Talgdrüsenkarzinom

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 6, Page 903-904, June 2024.
Jochen Utikal, Selma Ugurel
wiley   +1 more source

A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene.

, 2007
Muir-Torre syndrome (MTS) is a rare cancer-predisposing syndrome that is autosomal dominantly inherited and characterized by the development of sebaceous skin lesions (adenomas, epitheliomas, basaliomas and carcinomas).
Vernez, M., Hutter, P., Halkic, N., Bouzourene, H., Monnerat, C., Gugerli, O.   +5 more
core   +1 more source

Muir–Torre syndrome: case report

Revista da Sociedade Portuguesa de Dermatologia e Venereologia
Muir–Torre syndrome (MTS) is characterized by the association of at least one, but often multiple, sebaceous skin neoplasms, and at least one visceral neoplasm, usually colorectal.
Joana Heitor, Ana R. Afonso, Catarina Antunes, Catarina Correia, André Lencastre   +4 more
doaj  

Historical review of Lynch syndrome

Journal of Coloproctology, 2013
Lynch syndrome was formerly known as Hereditary Nonpolyposis Colorectal Cancer. Currently, these two nomenclatures each have their unique definitions and are no longer used interchangeably.
Andrew I. Wolf, Adam H. Buchanan, Linda M. Farkas   +2 more
doaj   +1 more source