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Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity

Leptomeningeal carcinomatosis (LMC) is exceedingly rare in gastric cancer. It is most commonly seen in breast, lung cancer and melanoma, and is associated with an extremely poor prognosis. If untreated, median overall survival is four to six weeks. No standard treatment for LMC exists and published...

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Autores principales: Baleiras, Mafalda Miranda, Graça, Joana, Fernandes, Leonor, Chorão, Martinha, Vasques, Ana Carolina, Pinto, Marta Mesquita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: UMF “Gr. T. Popa” Iasi Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066584/
https://www.ncbi.nlm.nih.gov/pubmed/35529092
http://dx.doi.org/10.22551/2022.34.0901.10196
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author Baleiras, Mafalda Miranda
Graça, Joana
Fernandes, Leonor
Chorão, Martinha
Vasques, Ana Carolina
Pinto, Marta Mesquita
author_facet Baleiras, Mafalda Miranda
Graça, Joana
Fernandes, Leonor
Chorão, Martinha
Vasques, Ana Carolina
Pinto, Marta Mesquita
author_sort Baleiras, Mafalda Miranda
collection PubMed
description Leptomeningeal carcinomatosis (LMC) is exceedingly rare in gastric cancer. It is most commonly seen in breast, lung cancer and melanoma, and is associated with an extremely poor prognosis. If untreated, median overall survival is four to six weeks. No standard treatment for LMC exists and published data are scarce. We present two cases of gastric carcinoma diagnosed with LMC that exemplify how aggressive this condition is and how short the time lapse is to perform any targeted therapy. This report aims to raise awareness of this rare metastatic possibility in gastric cancer and its diagnostic and therapeutic challenges.
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spelling pubmed-90665842022-05-06 Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity Baleiras, Mafalda Miranda Graça, Joana Fernandes, Leonor Chorão, Martinha Vasques, Ana Carolina Pinto, Marta Mesquita Arch Clin Cases Case Report Leptomeningeal carcinomatosis (LMC) is exceedingly rare in gastric cancer. It is most commonly seen in breast, lung cancer and melanoma, and is associated with an extremely poor prognosis. If untreated, median overall survival is four to six weeks. No standard treatment for LMC exists and published data are scarce. We present two cases of gastric carcinoma diagnosed with LMC that exemplify how aggressive this condition is and how short the time lapse is to perform any targeted therapy. This report aims to raise awareness of this rare metastatic possibility in gastric cancer and its diagnostic and therapeutic challenges. UMF “Gr. T. Popa” Iasi Publishing House 2022-04-06 /pmc/articles/PMC9066584/ /pubmed/35529092 http://dx.doi.org/10.22551/2022.34.0901.10196 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Baleiras, Mafalda Miranda
Graça, Joana
Fernandes, Leonor
Chorão, Martinha
Vasques, Ana Carolina
Pinto, Marta Mesquita
Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title_full Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title_fullStr Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title_full_unstemmed Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title_short Leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
title_sort leptomeningeal carcinomatosis in gastric cancer: a case report of a rare yet aggressive entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066584/
https://www.ncbi.nlm.nih.gov/pubmed/35529092
http://dx.doi.org/10.22551/2022.34.0901.10196
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