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Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease
Type I neurofibromatosis (NF-1) is a rare autosomal dominant disease. It can affect any organ system including vascular tissues. A 53 years old man, with a past medical history of NF-1, retinitis pigmentosa and hypertension attended to the emergency department for chest pain and palpitations and was...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elmer Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935525/ https://www.ncbi.nlm.nih.gov/pubmed/24578758 http://dx.doi.org/10.14740/jocmr1692w |
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author | Rodriguez-Guzman, Marcel Gallegos-Carrera, Belen Vicente-Antunes, Sara Fernandez-Ormaechea, Itziar Zapatero-Gaviria, Jose Villar-Alvarez, Felipe |
author_facet | Rodriguez-Guzman, Marcel Gallegos-Carrera, Belen Vicente-Antunes, Sara Fernandez-Ormaechea, Itziar Zapatero-Gaviria, Jose Villar-Alvarez, Felipe |
author_sort | Rodriguez-Guzman, Marcel |
collection | PubMed |
description | Type I neurofibromatosis (NF-1) is a rare autosomal dominant disease. It can affect any organ system including vascular tissues. A 53 years old man, with a past medical history of NF-1, retinitis pigmentosa and hypertension attended to the emergency department for chest pain and palpitations and was discharged 2 days after acute coronary syndrome was ruled out. During this admission an echocardiogram was performed which showed a left ventricular hypertrophy with normal ejection fraction and a chest X-ray which revealed no pathologic images. No invasive procedures were preformed. Three days after discharge, he returned to our hospital for sudden onset of oppressive chest pain in the right arm, irradiated to the ipsilateral shoulder, chest and back. After several tests, a diagnosis of hemothorax was made. Hemoglobin levels declined during the first 2 days of admission from 12.1 to 9.6 g/dL, although the patient remained hemodynamic stable. An arteriography was performed, which showed the presence of bleeding from a branch of the right subclavian artery, which was selectively catheterized and embolized with coils. Afterwards, a video-assisted thoracoscopy was made, in order to drain the hemothorax and to carry out a visual review of the pleural cavity. The patient had a good clinical and radiologic progression and was discharged after few days. After a year of follow-up, the patient has remained clinically asymptomatic with no further episodes of active bleeding. |
format | Online Article Text |
id | pubmed-3935525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39355252014-02-26 Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease Rodriguez-Guzman, Marcel Gallegos-Carrera, Belen Vicente-Antunes, Sara Fernandez-Ormaechea, Itziar Zapatero-Gaviria, Jose Villar-Alvarez, Felipe J Clin Med Res Case Report Type I neurofibromatosis (NF-1) is a rare autosomal dominant disease. It can affect any organ system including vascular tissues. A 53 years old man, with a past medical history of NF-1, retinitis pigmentosa and hypertension attended to the emergency department for chest pain and palpitations and was discharged 2 days after acute coronary syndrome was ruled out. During this admission an echocardiogram was performed which showed a left ventricular hypertrophy with normal ejection fraction and a chest X-ray which revealed no pathologic images. No invasive procedures were preformed. Three days after discharge, he returned to our hospital for sudden onset of oppressive chest pain in the right arm, irradiated to the ipsilateral shoulder, chest and back. After several tests, a diagnosis of hemothorax was made. Hemoglobin levels declined during the first 2 days of admission from 12.1 to 9.6 g/dL, although the patient remained hemodynamic stable. An arteriography was performed, which showed the presence of bleeding from a branch of the right subclavian artery, which was selectively catheterized and embolized with coils. Afterwards, a video-assisted thoracoscopy was made, in order to drain the hemothorax and to carry out a visual review of the pleural cavity. The patient had a good clinical and radiologic progression and was discharged after few days. After a year of follow-up, the patient has remained clinically asymptomatic with no further episodes of active bleeding. Elmer Press 2014-04 2014-02-06 /pmc/articles/PMC3935525/ /pubmed/24578758 http://dx.doi.org/10.14740/jocmr1692w Text en Copyright 2014, Rodriguez-Guzman et al. http://creativecommons.org/licenses/by/2.0/ 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 work is properly cited. |
spellingShingle | Case Report Rodriguez-Guzman, Marcel Gallegos-Carrera, Belen Vicente-Antunes, Sara Fernandez-Ormaechea, Itziar Zapatero-Gaviria, Jose Villar-Alvarez, Felipe Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title | Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title_full | Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title_fullStr | Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title_full_unstemmed | Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title_short | Spontaneous Hemothorax in a Patient With von Recklinghausen’s Disease |
title_sort | spontaneous hemothorax in a patient with von recklinghausen’s disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935525/ https://www.ncbi.nlm.nih.gov/pubmed/24578758 http://dx.doi.org/10.14740/jocmr1692w |
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