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...
Main Authors: | Yuan-Shao Chen, Yoon Bin Chong, Chih-Hung Lin, Ann-Shung Lieu |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Health/LWW
2019-01-01
|
Series: | Formosan Journal of Surgery |
Subjects: | |
Online Access: | http://www.e-fjs.org/article.asp?issn=1682-606X;year=2019;volume=52;issue=5;spage=197;epage=199;aulast=Chen |
Similar Items
-
Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
by: Hanane El Aggari, MD, et al.
Published: (2023-08-01) -
Lhermitte-Duclos disease: an extremely rare cerebellar tumor
by: Salah Bellasri, et al.
Published: (2017-09-01) -
Lhermitte-Duclos disease in a 51-year old patient
by: Amro Abdelrahman, MBBS, et al.
Published: (2024-07-01) -
A Case Report of Lhermitte-Duclos Disease in a 10-Month-Old Child Presenting with Hydrocephalus
by: Abhishek Tamrakar, et al.
Published: (2019-12-01) -
Lhermitte-Duclos Disease: A case report
by: Prakash Kafle, et al.
Published: (2017-03-01)