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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Dades bibliogràfiques
Autors principals:	Yuan-Shao Chen, Yoon Bin Chong, Chih-Hung Lin, Ann-Shung Lieu
Format:	Article
Idioma:	English
Publicat:	Wolters Kluwer Health/LWW 2019-01-01
Col·lecció:	Formosan Journal of Surgery
Matèries:	cowden syndrome dysplastic cerebellar gangliocytoma lhermitte–duclos disease
Accés en línia:	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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http://www.e-fjs.org/article.asp?issn=1682-606X;year=2019;volume=52;issue=5;spage=197;epage=199;aulast=Chen

Cowden syndrome diagnosed by Lhermitte–Duclos disease

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