Results 121 to 130 of about 1,372,625 (169)
Usefulness of PET/CT for early detection of internal malignancies in patients with Muir-Torre syndrome: report of two cases. [PDF]
Surg Case Rep, 2017 Ishiguro Y +11 more
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Two Different Dermoscopic Presentations of Sebaceous Adenoma in One Patient
Przegląd DermatologicznyUrszula Maińska +4 more
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Surgical resection and full-thickness skin grafting for sebaceoma extending into the external auditory canal: a case report. [PDF]
J Surg Case RepYoshimura M, Omori M.
europepmc +1 more source
The Lancet Oncology, 2005 Muir-Torre syndrome is an autosomal-dominant skin condition of genetic origin, characterised by tumours of the sebaceous gland or keratoacanthoma that are associated with visceral malignant diseases. The cutaneous characteristics of Muir-Torre syndrome are sebaceous adenoma, epithelioma, carcinoma, or multiple keratoacanthomas, whereas visceral ...
PONTI, Giovanni, PONZ DE LEON, Maurizio
openaire +4 more sources
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
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Journal of Dermatology, 1992
AbstractMuir‐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.
M Yokota, T Kanzaki, Tamotsu Kanzaki
exaly +3 more sources
AbstractMuir‐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.
M Yokota, T Kanzaki, Tamotsu Kanzaki
exaly +3 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
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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 ...
Paolo Angeli, Salvatore Piano
exaly +2 more sources
Der Hautarzt, 2001
The Muir-Torre syndrome (MTS) is a rare, autosomal-dominant inherited disease characterized by sebaceous gland tumors and at least one internal malignancy. In many cases a genetic defect known as microsatellite instability can be identified. Similar pathogenetic mechanisms are found in patients with the hereditary non-polyposis colon cancer syndrome ...
J, Körber, D, Djawari
+6 more sources
The Muir-Torre syndrome (MTS) is a rare, autosomal-dominant inherited disease characterized by sebaceous gland tumors and at least one internal malignancy. In many cases a genetic defect known as microsatellite instability can be identified. Similar pathogenetic mechanisms are found in patients with the hereditary non-polyposis colon cancer syndrome ...
J, Körber, D, Djawari
+6 more sources