Results 131 to 140 of about 1,372,625 (169)
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American Journal of Clinical Dermatology, 2007
In this case report of Muir-Torre syndrome (MTS), we describe a 47-year-old man with a personal and family history of colon cancer and a personal history of keratoacanthoma who presented with a sebaceous carcinoma and, subsequently, had a cystic sebaceous tumor.
Anne M, Lachiewicz +4 more
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In this case report of Muir-Torre syndrome (MTS), we describe a 47-year-old man with a personal and family history of colon cancer and a personal history of keratoacanthoma who presented with a sebaceous carcinoma and, subsequently, had a cystic sebaceous tumor.
Anne M, Lachiewicz +4 more
openaire +3 more sources
Annals of Plastic Surgery, 1998
Muir-Torre syndrome is a rare autosomal dominant disorder characterized by unusual sebaceous neoplasms and visceral malignancy. Excluding sebaceous hyperplasia and sebaceous nevus of Jadassohn, sebaceous neoplasms occur so rarely that the presence of a sebaceous neoplasm mandates consideration of Muir-Torre syndrome.
P J, Johnson, F, Heckler
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Muir-Torre syndrome is a rare autosomal dominant disorder characterized by unusual sebaceous neoplasms and visceral malignancy. Excluding sebaceous hyperplasia and sebaceous nevus of Jadassohn, sebaceous neoplasms occur so rarely that the presence of a sebaceous neoplasm mandates consideration of Muir-Torre syndrome.
P J, Johnson, F, Heckler
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Sebaceous adenoma arising within an ovarian mature cystic teratoma in Muir-Torre syndrome
Annals of Diagnostic Pathology, 2012 This is the first reported case of a sebaceous adenoma arising within an ovarian mature cystic teratoma in a patient with Muir-Torre syndrome. The pathologic findings and a literature review are presented, including the importance and possible benefits ...
Julie McGaughran, Jason Smith
exaly +2 more sources
Revista Clínica Española (English Edition), 2019
Muir-Torre syndrome (MTS) is an autosomal dominant disease with approximately 200 reported cases worldwide, which is characterised by multiple neoplasms of the skin and internal organs. This is a case report of a 57-year-old woman with MTS, who was referred to a plastic surgery department from a gastroenterology department due to a neoplasm of the skin.
M, Garayar Cantero +2 more
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Muir-Torre syndrome (MTS) is an autosomal dominant disease with approximately 200 reported cases worldwide, which is characterised by multiple neoplasms of the skin and internal organs. This is a case report of a 57-year-old woman with MTS, who was referred to a plastic surgery department from a gastroenterology department due to a neoplasm of the skin.
M, Garayar Cantero +2 more
openaire +4 more sources
Penile keratoacanthoma associated with urothelial carcinoma of the bladder in Muir-Torre syndrome
Urologic Oncology: Seminars and Original Investigations, 2007 A combination of some specific skin tumors with visceral cancers characterize Muir-Torre syndrome. A 60-year-old male patient who presented with penile keratoacanthoma accompanied by bladder and colorectal cancer is presented. (c) 2007 Elsevier Inc.
Mustafa Seçil +2 more
exaly +2 more sources
Journal of Surgical Oncology, 1986
AbstractThe patient with sebaceous skin tumors and visceral malignancies, Muir‐Torre syndrome, is presented. The documentation of tumors in 8 of 13 members in her kindred supports the concept that this syndrome represents a cancer‐disposing phenotype.
C, Shapiro +4 more
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AbstractThe patient with sebaceous skin tumors and visceral malignancies, Muir‐Torre syndrome, is presented. The documentation of tumors in 8 of 13 members in her kindred supports the concept that this syndrome represents a cancer‐disposing phenotype.
C, Shapiro +4 more
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Dermatologic Clinics, 1995
The Muir-Torre syndrome is an autosomal dominantly inherited genodermatosis with malignant potential that is characterized by the presence of at least one sebaceous gland tumor (adenoma, epithelioma, or carcinoma) and a minimum of one internal malignancy. The syndrome has been documented in 147 individuals. Associated features in some of the Muir-Torre
P R, Cohen +3 more
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The Muir-Torre syndrome is an autosomal dominantly inherited genodermatosis with malignant potential that is characterized by the presence of at least one sebaceous gland tumor (adenoma, epithelioma, or carcinoma) and a minimum of one internal malignancy. The syndrome has been documented in 147 individuals. Associated features in some of the Muir-Torre
P R, Cohen +3 more
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Journal of Cutaneous Pathology, 2017 Muir-Torre syndrome is a clinical variant of Lynch syndrome defined by the synchronous or metachronous occurrence of at least one sebaceous neoplasm and at least one Lynch syndrome-related internal cancer.
Brandon R Litzner
exaly +2 more sources
Skinmed, 2021
A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years. The patient has also had visceral cancer and had undergone a colon resection 17 years before to treat colon cancer and was recently diagnosed with ...
A Caresse, Gamret +7 more
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A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years. The patient has also had visceral cancer and had undergone a colon resection 17 years before to treat colon cancer and was recently diagnosed with ...
A Caresse, Gamret +7 more
openaire +1 more source
2010
Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that consists of unusual cutaneous sebaceous neoplasm, with or without kerathoacantomas and one or more low-grade visceral malignancies, with or without colonic polyps, in the absence of other predisposing factors.
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Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that consists of unusual cutaneous sebaceous neoplasm, with or without kerathoacantomas and one or more low-grade visceral malignancies, with or without colonic polyps, in the absence of other predisposing factors.
openaire +2 more sources