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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...

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Autores principales: Foster, Jessica B, Li, Dong, March, Michael E, Sheppard, Sarah E, Adams, Denise M, Hakonarson, Hakon, Dori, Yoav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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