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Kaposiform lymphangiomatosis effectively treated with MEK inhibition
Kaposiform lymphangiomatosis (KLA) is a rare lymphatic anomaly primarily affecting the mediastinum with high mortality rate. We present a patient with KLA and significant disease burden harboring a somatic point mutation in the Casitas B lineage lymphoma (CBL) gene. She was treated with MEK inhibiti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539180/ https://www.ncbi.nlm.nih.gov/pubmed/32894644 http://dx.doi.org/10.15252/emmm.202012324 |
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author | Foster, Jessica B Li, Dong March, Michael E Sheppard, Sarah E Adams, Denise M Hakonarson, Hakon Dori, Yoav |
author_facet | Foster, Jessica B Li, Dong March, Michael E Sheppard, Sarah E Adams, Denise M Hakonarson, Hakon Dori, Yoav |
author_sort | Foster, Jessica B |
collection | PubMed |
description | Kaposiform lymphangiomatosis (KLA) is a rare lymphatic anomaly primarily affecting the mediastinum with high mortality rate. We present a patient with KLA and significant disease burden harboring a somatic point mutation in the Casitas B lineage lymphoma (CBL) gene. She was treated with MEK inhibition with complete resolution of symptoms, near‐complete resolution of lymphatic fluid burden, and remodeling of her lymphatic system. While patients with KLA have been reported to harbor mutations in NRAS, here we report for the first time a causative mutation in the CBL gene in a patient with KLA, successfully treated with Ras pathway inhibition. |
format | Online Article Text |
id | pubmed-7539180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75391802020-10-09 Kaposiform lymphangiomatosis effectively treated with MEK inhibition Foster, Jessica B Li, Dong March, Michael E Sheppard, Sarah E Adams, Denise M Hakonarson, Hakon Dori, Yoav EMBO Mol Med Reports Kaposiform lymphangiomatosis (KLA) is a rare lymphatic anomaly primarily affecting the mediastinum with high mortality rate. We present a patient with KLA and significant disease burden harboring a somatic point mutation in the Casitas B lineage lymphoma (CBL) gene. She was treated with MEK inhibition with complete resolution of symptoms, near‐complete resolution of lymphatic fluid burden, and remodeling of her lymphatic system. While patients with KLA have been reported to harbor mutations in NRAS, here we report for the first time a causative mutation in the CBL gene in a patient with KLA, successfully treated with Ras pathway inhibition. John Wiley and Sons Inc. 2020-09-07 2020-10-07 /pmc/articles/PMC7539180/ /pubmed/32894644 http://dx.doi.org/10.15252/emmm.202012324 Text en ©2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reports Foster, Jessica B Li, Dong March, Michael E Sheppard, Sarah E Adams, Denise M Hakonarson, Hakon Dori, Yoav Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title | Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title_full | Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title_fullStr | Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title_full_unstemmed | Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title_short | Kaposiform lymphangiomatosis effectively treated with MEK inhibition |
title_sort | kaposiform lymphangiomatosis effectively treated with mek inhibition |
topic | Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539180/ https://www.ncbi.nlm.nih.gov/pubmed/32894644 http://dx.doi.org/10.15252/emmm.202012324 |
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