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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10250148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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