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Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis)
Generalised lymphatic anomaly (GLA), also known as lymphangiomatosis, is a rare disease caused by congenital abnormalities of lymphatic development. It usually presents in childhood but can also be diagnosed in adults. GLA encompasses a wide spectrum of clinical manifestations ranging from single-or...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487238/ https://www.ncbi.nlm.nih.gov/pubmed/27246594 http://dx.doi.org/10.1183/16000617.0018-2016 |
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author | Luisi, Francesca Torre, Olga Harari, Sergio |
author_facet | Luisi, Francesca Torre, Olga Harari, Sergio |
author_sort | Luisi, Francesca |
collection | PubMed |
description | Generalised lymphatic anomaly (GLA), also known as lymphangiomatosis, is a rare disease caused by congenital abnormalities of lymphatic development. It usually presents in childhood but can also be diagnosed in adults. GLA encompasses a wide spectrum of clinical manifestations ranging from single-organ involvement to generalised disease. Given the rarity of the disease, most of the information regarding it comes from case reports. To date, no clinical trials concerning treatment are available. This review focuses on thoracic GLA and summarises possible diagnostic and therapeutic approaches. |
format | Online Article Text |
id | pubmed-9487238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94872382022-11-14 Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) Luisi, Francesca Torre, Olga Harari, Sergio Eur Respir Rev Reviews Generalised lymphatic anomaly (GLA), also known as lymphangiomatosis, is a rare disease caused by congenital abnormalities of lymphatic development. It usually presents in childhood but can also be diagnosed in adults. GLA encompasses a wide spectrum of clinical manifestations ranging from single-organ involvement to generalised disease. Given the rarity of the disease, most of the information regarding it comes from case reports. To date, no clinical trials concerning treatment are available. This review focuses on thoracic GLA and summarises possible diagnostic and therapeutic approaches. European Respiratory Society 2016-06 /pmc/articles/PMC9487238/ /pubmed/27246594 http://dx.doi.org/10.1183/16000617.0018-2016 Text en Copyright ©ERS 2016. https://creativecommons.org/licenses/by-nc/4.0/ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. |
spellingShingle | Reviews Luisi, Francesca Torre, Olga Harari, Sergio Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title | Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title_full | Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title_fullStr | Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title_full_unstemmed | Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title_short | Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
title_sort | thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis) |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487238/ https://www.ncbi.nlm.nih.gov/pubmed/27246594 http://dx.doi.org/10.1183/16000617.0018-2016 |
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