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First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation

A 42-year-old female with a past medical history of femoral facial syndrome (FFS) and years of gastroesophageal reflux disease presented to our clinic with symptoms of dysphagia and iron deficiency anemia. On upper endoscopy, esophageal stricture and adenocarcinoma were detected. Unfortunately, the...

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Detalles Bibliográficos
Autores principales: Reyes, Cynthia A, Young, Juliana N, Torres, Paul R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123342/
https://www.ncbi.nlm.nih.gov/pubmed/35607579
http://dx.doi.org/10.7759/cureus.24285
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author Reyes, Cynthia A
Young, Juliana N
Torres, Paul R
author_facet Reyes, Cynthia A
Young, Juliana N
Torres, Paul R
author_sort Reyes, Cynthia A
collection PubMed
description A 42-year-old female with a past medical history of femoral facial syndrome (FFS) and years of gastroesophageal reflux disease presented to our clinic with symptoms of dysphagia and iron deficiency anemia. On upper endoscopy, esophageal stricture and adenocarcinoma were detected. Unfortunately, the patient developed coronavirus disease 2019 (COVID-19) multi-organ failure prior to cancer treatment and died with dignity after choosing comfort care measures. To the best of our knowledge, we report the first case of FFS in an adult patient. This case also uniquely highlights the rare gastrointestinal manifestations of FFS.
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spelling pubmed-91233422022-05-22 First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation Reyes, Cynthia A Young, Juliana N Torres, Paul R Cureus Pediatrics A 42-year-old female with a past medical history of femoral facial syndrome (FFS) and years of gastroesophageal reflux disease presented to our clinic with symptoms of dysphagia and iron deficiency anemia. On upper endoscopy, esophageal stricture and adenocarcinoma were detected. Unfortunately, the patient developed coronavirus disease 2019 (COVID-19) multi-organ failure prior to cancer treatment and died with dignity after choosing comfort care measures. To the best of our knowledge, we report the first case of FFS in an adult patient. This case also uniquely highlights the rare gastrointestinal manifestations of FFS. Cureus 2022-04-19 /pmc/articles/PMC9123342/ /pubmed/35607579 http://dx.doi.org/10.7759/cureus.24285 Text en Copyright © 2022, Reyes et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Reyes, Cynthia A
Young, Juliana N
Torres, Paul R
First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title_full First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title_fullStr First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title_full_unstemmed First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title_short First Reported Case of Femoral Facial Syndrome in an Adult: Esophageal Adenocarcinoma as a Progressive Gastrointestinal Manifestation
title_sort first reported case of femoral facial syndrome in an adult: esophageal adenocarcinoma as a progressive gastrointestinal manifestation
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123342/
https://www.ncbi.nlm.nih.gov/pubmed/35607579
http://dx.doi.org/10.7759/cureus.24285
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