Results 131 to 140 of about 3,333 (172)
European Journal of Plastic Surgery, 2004 Muir–Torre syndrome is a rare autosomal dominant disorder characterized by sebaceous neoplasms of skin and one or more malignancies of the visceral organs. The sebaceous neoplasms include sebaceous adenoma, sebaceous epithelioma, basal cell epithelioma, and sebaceous carcinoma [1]. Since these sebaceous neoplasms occur rarely, when they are recognized,
Alper Tuncel +2 more
core +4 more sources
Muir-Torre Syndrome: A Case Report
Tumori Journal, 1991 The authors present a case of Muir-Torre syndrome, the « sporadic » form, with a review of the literature. The importance of the close scrutiny of these patients and their relatives is stressed.
M, Bisceglia, P, Zenarola
openaire +3 more sources
The liver: another organ involved in Muir Torre syndrome?
Familial Cancer, 2011 Muir Torre syndrome is a rare autosomal dominant cancer-predisposing syndrome characterized by the occurrence of sebaceous gland neoplasms and/or keratoacanthomas associated with visceral malignancies that belong to the spectrum of hereditary non ...
F Morando +2 more
exaly +2 more sources
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 ...
Jason Smith
exaly +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +3 more sources
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
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
Russian Journal of Clinical Dermatology and Venereology, 2023
The clinical case of Muir-Torre syndrome in a patient with multifocal synchronous basal cell skin cancer with sebaceous differentiation and endometrial cancer in a medical history, including clinical manifestations and dermatoscopic pattern features of sebaceous adenoma, epithelioma with sebaceous glandular differentiation and sebaceous glandular skin ...
T.G. Sedova, V.D. Elkin
openaire +1 more source
The clinical case of Muir-Torre syndrome in a patient with multifocal synchronous basal cell skin cancer with sebaceous differentiation and endometrial cancer in a medical history, including clinical manifestations and dermatoscopic pattern features of sebaceous adenoma, epithelioma with sebaceous glandular differentiation and sebaceous glandular skin ...
T.G. Sedova, V.D. Elkin
openaire +1 more source
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, Claudia I Vidal
exaly +1 more source