Cowden syndrome diagnosed by Lhermitte–Duclos disease

Cowden syndrome diagnosed by Lhermitte–Duclos disease

Cowden syndrome (CS) is a rare genetic disease which puts patients at an increased risk of developing mucocutaneous lesion, multiple hamartomas, breast cancer, thyroid cancer, and Lhermitte–Duclos disease (LDD). This article reviews the role of LDD in the diagnosis of CS. It is important for all cli...

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Autori principali: Yuan-Shao Chen, Yoon Bin Chong, Chih-Hung Lin, Ann-Shung Lieu
Natura: Articolo
Lingua:English
Pubblicazione: Wolters Kluwer Health/LWW 2019-01-01
Serie:Formosan Journal of Surgery
Soggetti:
cowden syndrome
dysplastic cerebellar gangliocytoma
lhermitte–duclos disease
Accesso online:http://www.e-fjs.org/article.asp?issn=1682-606X;year=2019;volume=52;issue=5;spage=197;epage=199;aulast=Chen

Accesso online

http://www.e-fjs.org/article.asp?issn=1682-606X;year=2019;volume=52;issue=5;spage=197;epage=199;aulast=Chen

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