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Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder

The dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease, is an uncommon hamartomatous lesion in the posterior fossa with some distinctive neuroradiological characteristics. It can happen in combination with Cowden syndrome or sporadically. Cowden disease, or multiple h...

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Autores principales: Aggari, Hanane El, Nasri, Siham, Zohra, Ahsayen Fatima, Aichouni, Narjisse, Kamaoui, Imane, Skiker, Imane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250148/
https://www.ncbi.nlm.nih.gov/pubmed/37304316
http://dx.doi.org/10.1016/j.radcr.2023.05.013
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author Aggari, Hanane El
Nasri, Siham
Zohra, Ahsayen Fatima
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
author_facet Aggari, Hanane El
Nasri, Siham
Zohra, Ahsayen Fatima
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
author_sort Aggari, Hanane El
collection PubMed
description The dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease, is an uncommon hamartomatous lesion in the posterior fossa with some distinctive neuroradiological characteristics. It can happen in combination with Cowden syndrome or sporadically. Cowden disease, or multiple hamartoma-neoplasia syndrome, is a rare autosomal dominant condition which is characterized by mucocutaneous lesions and systemic malignancies. We present a case of Lhermitte-Duclos disease and Cowden disease occurring in adult patients. The clinical and radiological features as well as the management approaches of this unusual disease complex are addressed.
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spelling pubmed-102501482023-06-10 Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder Aggari, Hanane El Nasri, Siham Zohra, Ahsayen Fatima Aichouni, Narjisse Kamaoui, Imane Skiker, Imane Radiol Case Rep Case Report The dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease, is an uncommon hamartomatous lesion in the posterior fossa with some distinctive neuroradiological characteristics. It can happen in combination with Cowden syndrome or sporadically. Cowden disease, or multiple hamartoma-neoplasia syndrome, is a rare autosomal dominant condition which is characterized by mucocutaneous lesions and systemic malignancies. We present a case of Lhermitte-Duclos disease and Cowden disease occurring in adult patients. The clinical and radiological features as well as the management approaches of this unusual disease complex are addressed. Elsevier 2023-06-06 /pmc/articles/PMC10250148/ /pubmed/37304316 http://dx.doi.org/10.1016/j.radcr.2023.05.013 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Aggari, Hanane El
Nasri, Siham
Zohra, Ahsayen Fatima
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title_full Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title_fullStr Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title_full_unstemmed Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title_short Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder
title_sort association between cowden syndrome and lhermitte-duclos disease: a case report of an uncommon genetic hamartomatous disorder
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250148/
https://www.ncbi.nlm.nih.gov/pubmed/37304316
http://dx.doi.org/10.1016/j.radcr.2023.05.013
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