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Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis
A 77‐year‐old woman presented to our hospital with complaints of persistent cough and low‐grade fever for two months. On radiological analysis, she had moderate right‐sided pleural effusion with right hilar and subcarinal lymphadenopathies. Thoracentesis showed chylothorax of unknown cause. Bronchos...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301284/ https://www.ncbi.nlm.nih.gov/pubmed/32566230 http://dx.doi.org/10.1002/rcr2.600 |
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author | Honda, Kojiro Saraya, Takeshi Miyaoka, Chika Suda, Kazuharu Fujiwara, Masachika Ishii, Haruyuki |
author_facet | Honda, Kojiro Saraya, Takeshi Miyaoka, Chika Suda, Kazuharu Fujiwara, Masachika Ishii, Haruyuki |
author_sort | Honda, Kojiro |
collection | PubMed |
description | A 77‐year‐old woman presented to our hospital with complaints of persistent cough and low‐grade fever for two months. On radiological analysis, she had moderate right‐sided pleural effusion with right hilar and subcarinal lymphadenopathies. Thoracentesis showed chylothorax of unknown cause. Bronchoscopy revealed a non‐specific inflammatory process. However, thoracoscopic surgery demonstrated a curiously enlarged lymphatic duct with its proximal portion compressed by subcarinal lymphadenopathies, pathologically diagnosed as granulomatous lymphadenitis. Hence, tuberculous lymphadenitis was proven to be the cause of chylothorax. Interestingly, cauterization of the lymphatic duct decreased the total amount of right‐sided pleural effusion along with a change in colour from milky yellow to red. These were in favour of tuberculosis (TB)‐associated chylothorax with the advent of the TB pleuritis. All symptoms and pleural effusion disappeared after the initiation of anti‐tuberculous drugs. The present case showed definite evidence of TB‐associated chylothorax development mechanism via compression of the lymphatic duct by mediastinal lymphadenopathies. |
format | Online Article Text |
id | pubmed-7301284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73012842020-06-19 Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis Honda, Kojiro Saraya, Takeshi Miyaoka, Chika Suda, Kazuharu Fujiwara, Masachika Ishii, Haruyuki Respirol Case Rep Case Reports A 77‐year‐old woman presented to our hospital with complaints of persistent cough and low‐grade fever for two months. On radiological analysis, she had moderate right‐sided pleural effusion with right hilar and subcarinal lymphadenopathies. Thoracentesis showed chylothorax of unknown cause. Bronchoscopy revealed a non‐specific inflammatory process. However, thoracoscopic surgery demonstrated a curiously enlarged lymphatic duct with its proximal portion compressed by subcarinal lymphadenopathies, pathologically diagnosed as granulomatous lymphadenitis. Hence, tuberculous lymphadenitis was proven to be the cause of chylothorax. Interestingly, cauterization of the lymphatic duct decreased the total amount of right‐sided pleural effusion along with a change in colour from milky yellow to red. These were in favour of tuberculosis (TB)‐associated chylothorax with the advent of the TB pleuritis. All symptoms and pleural effusion disappeared after the initiation of anti‐tuberculous drugs. The present case showed definite evidence of TB‐associated chylothorax development mechanism via compression of the lymphatic duct by mediastinal lymphadenopathies. John Wiley & Sons, Ltd 2020-06-18 /pmc/articles/PMC7301284/ /pubmed/32566230 http://dx.doi.org/10.1002/rcr2.600 Text en © 2020 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Honda, Kojiro Saraya, Takeshi Miyaoka, Chika Suda, Kazuharu Fujiwara, Masachika Ishii, Haruyuki Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title | Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title_full | Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title_fullStr | Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title_full_unstemmed | Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title_short | Tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
title_sort | tuberculosis‐associated chylothorax revealing an enlarged lymphatic duct due to tuberculosis lymphadenitis |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301284/ https://www.ncbi.nlm.nih.gov/pubmed/32566230 http://dx.doi.org/10.1002/rcr2.600 |
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