Literature DB >> 11531761

Lhermitte-Duclos disease associated with Cowden's syndrome: case report and literature review.

C Murray1, P Shipman, M Khangure, T Chakera, P Robbins, W McAuliffe, S Davis.   

Abstract

Lhermitte-Duclos disease (LDD) is a rare entity that may occur in the setting of Cowden's syndrome (CS). Accurate preoperative diagnosis can be made on the characteristic CT and MR appearances, thereby obviating the need for biopsy. It is important to be aware of the link between LDD and CS so that appropriate genetic counselling and tumour surveillance can be undertaken.

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Year:  2001        PMID: 11531761     DOI: 10.1046/j.1440-1673.2001.00933.x

Source DB:  PubMed          Journal:  Australas Radiol        ISSN: 0004-8461


  4 in total

1.  Lhermitte-Duclos disease. A case report.

Authors:  Andrea Giorgianni; Carlo Pellegrino; Alessandro De Benedictis; Anna Mercuri; Fabio Baruzzi; Renzo Minotto; Antonio Tabano; Sergio Balbi
Journal:  Neuroradiol J       Date:  2013-12-18

2.  MR imaging and spectroscopy in Lhermitte-Duclos disease.

Authors:  S Nagaraja; T Powell; P D Griffiths; I D Wilkinson
Journal:  Neuroradiology       Date:  2004-04-21       Impact factor: 2.804

3.  L'hermitte-Duclos disease in an elderly patient: A case report and review of the literature.

Authors:  Ersin Ozeren; Levent Gurses; Mehmet Sorar; Uygur Er; Evrim Önder; Ata Türker Arıkök
Journal:  Asian J Neurosurg       Date:  2014 Oct-Dec

4.  Intracranial hypertension and cerebellar symptoms due to Lhermitte-Duclos disease.

Authors:  Farhad Assarzadegan; Atoosa Gharib; Shirin Behbahani; Meysam Ebrahimi-Abyaneh
Journal:  Iran J Neurol       Date:  2015-04-04
  4 in total

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