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Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition

The RASopathies are a group of genetic conditions resulting from mutations within the RAS/mitogen-activated protein kinase (RAS-MAPK) pathway. Lymphatic abnormalities are commonly associated with these conditions, however central conducting lymphatic abnormalities (CCLA) have only recently been desc...

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Autores principales: Gordon, Kristiana, Moore, Matthew, Van Zanten, Malou, Pearce, Julian, Itkin, Maxim, Madden, Brendan, Ratnam, Lakshmi, Mortimer, Peter S., Nagaraja, Rani, Mansour, Sahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550924/
https://www.ncbi.nlm.nih.gov/pubmed/36238151
http://dx.doi.org/10.3389/fgene.2022.1001105
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author Gordon, Kristiana
Moore, Matthew
Van Zanten, Malou
Pearce, Julian
Itkin, Maxim
Madden, Brendan
Ratnam, Lakshmi
Mortimer, Peter S.
Nagaraja, Rani
Mansour, Sahar
author_facet Gordon, Kristiana
Moore, Matthew
Van Zanten, Malou
Pearce, Julian
Itkin, Maxim
Madden, Brendan
Ratnam, Lakshmi
Mortimer, Peter S.
Nagaraja, Rani
Mansour, Sahar
author_sort Gordon, Kristiana
collection PubMed
description The RASopathies are a group of genetic conditions resulting from mutations within the RAS/mitogen-activated protein kinase (RAS-MAPK) pathway. Lymphatic abnormalities are commonly associated with these conditions, however central conducting lymphatic abnormalities (CCLA) have only recently been described. CCLAs may be progressive and can result in devastating systemic sequelae, such as recurrent chylothoraces, chylopericardium and chylous ascites which can cause significant morbidity and even mortality. Improvements in imaging modalities of the central lymphatics have enhanced our understanding of these complex abnormalities. Management is challenging and have mainly consisted of diuretics and invasive mechanical drainages. We describe two adult males with Noonan syndrome with a severe and progressive CCLA. In one patient we report the therapeutic role of targeted molecular therapy with the MEK inhibitor ‘Trametinib’, which has resulted in dramatic, and sustained, clinical improvement. The successful use of MEK inhibition highlights the importance of understanding the molecular cause of lymphatic abnormalities and utilising targeted therapies to improve quality of life and potentially life expectancy.
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spelling pubmed-95509242022-10-12 Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition Gordon, Kristiana Moore, Matthew Van Zanten, Malou Pearce, Julian Itkin, Maxim Madden, Brendan Ratnam, Lakshmi Mortimer, Peter S. Nagaraja, Rani Mansour, Sahar Front Genet Genetics The RASopathies are a group of genetic conditions resulting from mutations within the RAS/mitogen-activated protein kinase (RAS-MAPK) pathway. Lymphatic abnormalities are commonly associated with these conditions, however central conducting lymphatic abnormalities (CCLA) have only recently been described. CCLAs may be progressive and can result in devastating systemic sequelae, such as recurrent chylothoraces, chylopericardium and chylous ascites which can cause significant morbidity and even mortality. Improvements in imaging modalities of the central lymphatics have enhanced our understanding of these complex abnormalities. Management is challenging and have mainly consisted of diuretics and invasive mechanical drainages. We describe two adult males with Noonan syndrome with a severe and progressive CCLA. In one patient we report the therapeutic role of targeted molecular therapy with the MEK inhibitor ‘Trametinib’, which has resulted in dramatic, and sustained, clinical improvement. The successful use of MEK inhibition highlights the importance of understanding the molecular cause of lymphatic abnormalities and utilising targeted therapies to improve quality of life and potentially life expectancy. Frontiers Media S.A. 2022-09-27 /pmc/articles/PMC9550924/ /pubmed/36238151 http://dx.doi.org/10.3389/fgene.2022.1001105 Text en Copyright © 2022 Gordon, Moore, Van Zanten, Pearce, Itkin, Madden, Ratnam, Mortimer, Nagaraja and Mansour. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Gordon, Kristiana
Moore, Matthew
Van Zanten, Malou
Pearce, Julian
Itkin, Maxim
Madden, Brendan
Ratnam, Lakshmi
Mortimer, Peter S.
Nagaraja, Rani
Mansour, Sahar
Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title_full Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title_fullStr Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title_full_unstemmed Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title_short Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
title_sort case report: progressive central conducting lymphatic abnormalities in the rasopathies. two case reports, including successful treatment by mek inhibition
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550924/
https://www.ncbi.nlm.nih.gov/pubmed/36238151
http://dx.doi.org/10.3389/fgene.2022.1001105
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