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A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication

Obstruction of the thoracic duct may lead to accumulation of a lymphatic fluid rich in triglycerides named chyle. When chyle accumulates in the pleural cavity, it becomes a chylothorax. Malignancy, particularly lymphoma, is the most common cause of chylothorax; however, any pathology leading to obst...

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Autores principales: Bhattarai, Bikash, Schmidt, Frances, Devkota, Ashok, Policard, Geraldine, Manhas, Saveena, Oke, Vikram, Agu, Chidozie Charles, Basunia, Md Rawshan, Enriquez, Danilo, Quist, Joseph, Kharel, Prakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558282/
https://www.ncbi.nlm.nih.gov/pubmed/26333861
http://dx.doi.org/10.3402/jchimp.v5.28300
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author Bhattarai, Bikash
Schmidt, Frances
Devkota, Ashok
Policard, Geraldine
Manhas, Saveena
Oke, Vikram
Agu, Chidozie Charles
Basunia, Md Rawshan
Enriquez, Danilo
Quist, Joseph
Kharel, Prakash
author_facet Bhattarai, Bikash
Schmidt, Frances
Devkota, Ashok
Policard, Geraldine
Manhas, Saveena
Oke, Vikram
Agu, Chidozie Charles
Basunia, Md Rawshan
Enriquez, Danilo
Quist, Joseph
Kharel, Prakash
author_sort Bhattarai, Bikash
collection PubMed
description Obstruction of the thoracic duct may lead to accumulation of a lymphatic fluid rich in triglycerides named chyle. When chyle accumulates in the pleural cavity, it becomes a chylothorax. Malignancy, particularly lymphoma, is the most common cause of chylothorax; however, any pathology leading to obstruction or destruction of the thoracic duct can lead to a chylothorax. This particular case investigates an incidence of chylothorax in sarcoidosis. A 54-year-old African American woman with a medical history of sarcoidosis, congestive heart failure, and smoking presented to the emergency department with complaints of bilateral foot swelling and exertional shortness of breath 3 days in duration. Physical examination was positive for bilateral crepitations with decreased air entry, abdominal ascites, and bilateral 2+ pitting edema. Both chest X-ray and chest CT were positive for stable bilateral pleural effusions (when compared to imaging done 3 years previously), and thoracocentesis and paracentesis were positive for chylous fluid accumulation. Chylothorax was diagnosed, and based on the previous medical history, the lymphadenopathy of sarcoidosis was determined to cause the occlusion of the thoracic duct. Lymphoscintigraphy and surgical intervention were advised; however, the family decided on conservative management and the patient expired intubated in the ICU. Chylothorax is a rare manifestation of sarcoidosis and high index of suspicion should be there to diagnose this, as there is high morbidity and mortality associated with it.
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spelling pubmed-45582822015-09-29 A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication Bhattarai, Bikash Schmidt, Frances Devkota, Ashok Policard, Geraldine Manhas, Saveena Oke, Vikram Agu, Chidozie Charles Basunia, Md Rawshan Enriquez, Danilo Quist, Joseph Kharel, Prakash J Community Hosp Intern Med Perspect Case Report Obstruction of the thoracic duct may lead to accumulation of a lymphatic fluid rich in triglycerides named chyle. When chyle accumulates in the pleural cavity, it becomes a chylothorax. Malignancy, particularly lymphoma, is the most common cause of chylothorax; however, any pathology leading to obstruction or destruction of the thoracic duct can lead to a chylothorax. This particular case investigates an incidence of chylothorax in sarcoidosis. A 54-year-old African American woman with a medical history of sarcoidosis, congestive heart failure, and smoking presented to the emergency department with complaints of bilateral foot swelling and exertional shortness of breath 3 days in duration. Physical examination was positive for bilateral crepitations with decreased air entry, abdominal ascites, and bilateral 2+ pitting edema. Both chest X-ray and chest CT were positive for stable bilateral pleural effusions (when compared to imaging done 3 years previously), and thoracocentesis and paracentesis were positive for chylous fluid accumulation. Chylothorax was diagnosed, and based on the previous medical history, the lymphadenopathy of sarcoidosis was determined to cause the occlusion of the thoracic duct. Lymphoscintigraphy and surgical intervention were advised; however, the family decided on conservative management and the patient expired intubated in the ICU. Chylothorax is a rare manifestation of sarcoidosis and high index of suspicion should be there to diagnose this, as there is high morbidity and mortality associated with it. Co-Action Publishing 2015-09-01 /pmc/articles/PMC4558282/ /pubmed/26333861 http://dx.doi.org/10.3402/jchimp.v5.28300 Text en © 2015 Bikash Bhattarai et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bhattarai, Bikash
Schmidt, Frances
Devkota, Ashok
Policard, Geraldine
Manhas, Saveena
Oke, Vikram
Agu, Chidozie Charles
Basunia, Md Rawshan
Enriquez, Danilo
Quist, Joseph
Kharel, Prakash
A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title_full A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title_fullStr A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title_full_unstemmed A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title_short A case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
title_sort case of chylothorax in a patient with sarcoidosis: a rare and potentially fatal complication
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558282/
https://www.ncbi.nlm.nih.gov/pubmed/26333861
http://dx.doi.org/10.3402/jchimp.v5.28300
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