|
|
|
|
Syndrome in question
|
|
|
|
|
|
|
|
نویسنده
|
pousa c.m.f.l. ,lavorato f.g. ,rehfeldt f.v. ,mann d. ,alves m.f.g.s.
|
|
منبع
|
journal brazilian annals of dermatology - 2015 - دوره : 90 - شماره : 5 - صفحه:759 -761
|
|
چکیده
|
Muir-torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia,but with no predisposing factors. the sebaceous neoplasm may appear before,during or after the diagnosis of colorectal cancer. as it is regarded as a subtype of nonpolyposis hereditary colorectal cancer,it is important to evaluate the patient’s first-degree relatives. the clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. we report the case of a patient who,after a tenyear diagnosis of colorectal cancer,presented with multiple sebaceous neoplasms. © 2015 by anais brasileiros de dermatologia.
|
|
کلیدواژه
|
Colorectal neoplasms; Hereditary nonpolyposis; Muir-torre syndrome; Sebaceous gland neoplasms; Skin neoplasms; Syndrome
|
|
آدرس
|
acre state hospital foundation,rio branco,ac, Brazil, private practice,rio de janeiro,rj, Brazil, jesus municipal hospital,rio de janeiro,rj,brazil,grande rio university (unigranrio),rio de janeiro,rj, Brazil, lagoa federal hospital,rio de janeiro, Brazil, state university of rio de janeiro (uerj),rio de janeiro,rj, Brazil
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Authors
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|