Cargando…

Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review

Leptomeningeal carcinomatosis, leptomeningeal meningitis, or, as referred here, leptomeningeal metastasis (LM), is a rare but frequently fatal complication seen in advanced stage of cancer either locally advanced or after a metastasis of a known primary cancer. We present a rare and uncommon case of...

Descripción completa

Detalles Bibliográficos
Autores principales: Moosavi, Leila, D’Assumpcao, Carlos, Bowen, Jonathan, Heidari, Arash, Cobos, Everardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699001/
https://www.ncbi.nlm.nih.gov/pubmed/31423841
http://dx.doi.org/10.1177/2324709619869380
_version_ 1783444650079551488
author Moosavi, Leila
D’Assumpcao, Carlos
Bowen, Jonathan
Heidari, Arash
Cobos, Everardo
author_facet Moosavi, Leila
D’Assumpcao, Carlos
Bowen, Jonathan
Heidari, Arash
Cobos, Everardo
author_sort Moosavi, Leila
collection PubMed
description Leptomeningeal carcinomatosis, leptomeningeal meningitis, or, as referred here, leptomeningeal metastasis (LM), is a rare but frequently fatal complication seen in advanced stage of cancer either locally advanced or after a metastasis of a known primary cancer. We present a rare and uncommon case of leptomeningeal metastases from carcinoma of unknown primary. A 32-year-old female was diagnosed with LM; however, no known primary carcinoma was identified after 2 separate biopsies. The first biopsy of the right pre-tracheal lymph node showed poorly differentiated pan-keratin (AE1 and AE3) and placental alkaline phosphatase with the possibility of germ cell origin. Second cytology of cervical lymphadenopathy was remarkable for cytokeratin 7 and 20, placental alkaline phosphatase, and CDX2 suggestive of germ line tumor with both mucinous ovarian and gastrointestinal carcinomas. Unfortunately, the LM progressed rapidly despite multiple cycles of germ cell origin directed systemic and intrathecal chemotherapy, and the patient opted for hospice care without getting a chance to identify the primary source.
format Online
Article
Text
id pubmed-6699001
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-66990012019-08-26 Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review Moosavi, Leila D’Assumpcao, Carlos Bowen, Jonathan Heidari, Arash Cobos, Everardo J Investig Med High Impact Case Rep Case Report Leptomeningeal carcinomatosis, leptomeningeal meningitis, or, as referred here, leptomeningeal metastasis (LM), is a rare but frequently fatal complication seen in advanced stage of cancer either locally advanced or after a metastasis of a known primary cancer. We present a rare and uncommon case of leptomeningeal metastases from carcinoma of unknown primary. A 32-year-old female was diagnosed with LM; however, no known primary carcinoma was identified after 2 separate biopsies. The first biopsy of the right pre-tracheal lymph node showed poorly differentiated pan-keratin (AE1 and AE3) and placental alkaline phosphatase with the possibility of germ cell origin. Second cytology of cervical lymphadenopathy was remarkable for cytokeratin 7 and 20, placental alkaline phosphatase, and CDX2 suggestive of germ line tumor with both mucinous ovarian and gastrointestinal carcinomas. Unfortunately, the LM progressed rapidly despite multiple cycles of germ cell origin directed systemic and intrathecal chemotherapy, and the patient opted for hospice care without getting a chance to identify the primary source. SAGE Publications 2019-08-17 /pmc/articles/PMC6699001/ /pubmed/31423841 http://dx.doi.org/10.1177/2324709619869380 Text en © 2019 American Federation for Medical Research http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Moosavi, Leila
D’Assumpcao, Carlos
Bowen, Jonathan
Heidari, Arash
Cobos, Everardo
Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title_full Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title_fullStr Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title_full_unstemmed Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title_short Leptomeningeal Carcinomatosis From Carcinoma of Unknown Primary in a Young Patient: A Case Report and a Literature Review
title_sort leptomeningeal carcinomatosis from carcinoma of unknown primary in a young patient: a case report and a literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699001/
https://www.ncbi.nlm.nih.gov/pubmed/31423841
http://dx.doi.org/10.1177/2324709619869380
work_keys_str_mv AT moosavileila leptomeningealcarcinomatosisfromcarcinomaofunknownprimaryinayoungpatientacasereportandaliteraturereview
AT dassumpcaocarlos leptomeningealcarcinomatosisfromcarcinomaofunknownprimaryinayoungpatientacasereportandaliteraturereview
AT bowenjonathan leptomeningealcarcinomatosisfromcarcinomaofunknownprimaryinayoungpatientacasereportandaliteraturereview
AT heidariarash leptomeningealcarcinomatosisfromcarcinomaofunknownprimaryinayoungpatientacasereportandaliteraturereview
AT coboseverardo leptomeningealcarcinomatosisfromcarcinomaofunknownprimaryinayoungpatientacasereportandaliteraturereview