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The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax

We present the case of a 19-year-old female with Ullrich congenital muscular dystrophy (UCMD1, a collagen VI defect) who developed a right-sided pneumothorax after choking on a piece of meat. She received two chest tubes (pigtails) that resolved the pneumothorax. She was discharged in stable conditi...

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Autores principales: Navas Nazario, Aledie, Cooper, Felicia I, Weber-Guzman, Fabiola, Finkel, Richard S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262640/
https://www.ncbi.nlm.nih.gov/pubmed/35812575
http://dx.doi.org/10.7759/cureus.25961
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author Navas Nazario, Aledie
Cooper, Felicia I
Weber-Guzman, Fabiola
Finkel, Richard S
author_facet Navas Nazario, Aledie
Cooper, Felicia I
Weber-Guzman, Fabiola
Finkel, Richard S
author_sort Navas Nazario, Aledie
collection PubMed
description We present the case of a 19-year-old female with Ullrich congenital muscular dystrophy (UCMD1, a collagen VI defect) who developed a right-sided pneumothorax after choking on a piece of meat. She received two chest tubes (pigtails) that resolved the pneumothorax. She was discharged in stable condition, and a chest radiograph two weeks later showed total resolution of the pneumothorax. Two months after this episode, the patient presented with another small, right-sided pneumothorax that shortly progressed to extension throughout the right side of the chest. These pneumothoraces were treated with three different pigtails, but this intervention was ineffective. Providers chose to utilize an autologous blood patch, which is an injection of the patient’s own blood instilled in the pleural cavity through a chest drain. The blood forms a clot and subsequently seals the lung tissues through inflammation. This technique was chosen because the patient had advanced neuromuscular weakness with chronic respiratory failure. Also, our patient was not a candidate for chemical or surgical pleurodesis due to the nature of the persistent pneumothorax and the underlying lung fibrosis and collagen defect. Subsequent reaccumulation of the pneumothorax led to a second blood patch procedure, which proved effective. The patient recovered and was discharged in stable condition with no further episodes of pneumothorax over the subsequent 14 months from the initial episode.
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spelling pubmed-92626402022-07-09 The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax Navas Nazario, Aledie Cooper, Felicia I Weber-Guzman, Fabiola Finkel, Richard S Cureus Neurology We present the case of a 19-year-old female with Ullrich congenital muscular dystrophy (UCMD1, a collagen VI defect) who developed a right-sided pneumothorax after choking on a piece of meat. She received two chest tubes (pigtails) that resolved the pneumothorax. She was discharged in stable condition, and a chest radiograph two weeks later showed total resolution of the pneumothorax. Two months after this episode, the patient presented with another small, right-sided pneumothorax that shortly progressed to extension throughout the right side of the chest. These pneumothoraces were treated with three different pigtails, but this intervention was ineffective. Providers chose to utilize an autologous blood patch, which is an injection of the patient’s own blood instilled in the pleural cavity through a chest drain. The blood forms a clot and subsequently seals the lung tissues through inflammation. This technique was chosen because the patient had advanced neuromuscular weakness with chronic respiratory failure. Also, our patient was not a candidate for chemical or surgical pleurodesis due to the nature of the persistent pneumothorax and the underlying lung fibrosis and collagen defect. Subsequent reaccumulation of the pneumothorax led to a second blood patch procedure, which proved effective. The patient recovered and was discharged in stable condition with no further episodes of pneumothorax over the subsequent 14 months from the initial episode. Cureus 2022-06-15 /pmc/articles/PMC9262640/ /pubmed/35812575 http://dx.doi.org/10.7759/cureus.25961 Text en Copyright © 2022, Navas Nazario 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 Neurology
Navas Nazario, Aledie
Cooper, Felicia I
Weber-Guzman, Fabiola
Finkel, Richard S
The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title_full The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title_fullStr The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title_full_unstemmed The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title_short The Use of Autologous Blood Patch in Ullrich Muscular Dystrophy and Recurrent Pneumothorax
title_sort use of autologous blood patch in ullrich muscular dystrophy and recurrent pneumothorax
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262640/
https://www.ncbi.nlm.nih.gov/pubmed/35812575
http://dx.doi.org/10.7759/cureus.25961
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