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Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature

BACKGROUND: Dieulafoy’s disease of the bronchus can cause massive and even fatal hemoptysis. Even though it is rare, it should be considered by physicians all over the world. This paper reports a case of bronchial Dieulafoy’s disease and summarizes the data of similar cases reported in literature. M...

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Autores principales: Daboussi, Salsabil, kacem, Marwa, Boubaker, Nouha, Chaabene, Mariem, Aichaouia, Chiraz, Mhamdi, Samira, Moatemri, Zied
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318670/
https://www.ncbi.nlm.nih.gov/pubmed/37403165
http://dx.doi.org/10.1186/s13019-023-02242-0
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author Daboussi, Salsabil
kacem, Marwa
Boubaker, Nouha
Chaabene, Mariem
Aichaouia, Chiraz
Mhamdi, Samira
Moatemri, Zied
author_facet Daboussi, Salsabil
kacem, Marwa
Boubaker, Nouha
Chaabene, Mariem
Aichaouia, Chiraz
Mhamdi, Samira
Moatemri, Zied
author_sort Daboussi, Salsabil
collection PubMed
description BACKGROUND: Dieulafoy’s disease of the bronchus can cause massive and even fatal hemoptysis. Even though it is rare, it should be considered by physicians all over the world. This paper reports a case of bronchial Dieulafoy’s disease and summarizes the data of similar cases reported in literature. METHODS: We report a case of bronchial Dieulafoy’s disease (BDD) in Tunisia. We also present a review of literature related to BDD from 1995 to 2022 using the PubMed, Google Scholar, web of science and Chinese National Knowledge Infrastructure Databases. Clinical characteristics, chest imaging, bronchoscopic and angiographic findings were summarized. Treatment courses were identified as well as patients’ outcome. RESULTS: We report the case of a 41-year-old man, so far in good health, presenting with massive hemoptysis. Bronchoscopy showed blood clots and a protruding lesion covered by mucosa with a white pointed cap at the entrance of the right upper lobe. Biopsies were not attempted. Embolization of bronchial artery was first realized and was not successful, with post procedure complications. Surgical intervention stopped the bleeding and pathological examination of the resected specimen confirmed Dieulafoy’s disease of the bronchus. Ninety cases of BDD were reported from 1995 to 2022. The main symptom was hemoptysis. Chest imaging findings were not specific. The diagnosis of BDD was mainly based on the bronchoscopy, branchial angiography and pathological findings or surgical specimens. Bronchoscopy findings were mostly nodular or prominent lesions (52.4%). Twenty-eight patients underwent bronchoscopic biopsies, 20 had massive bleeding and 10 died. Bronchial angiography mainly showed tortuous and dilation of bronchial artery, and the lesions were mainly located in the right bronchus. Selective bronchial artery embolization (SBAE) was performed in 32 patients and 39 patients underwent surgery. CONCLUSION: To our knowledge, this is the first case of bronchial Dieulafoy’s disease to be reported in Tunisia and North Africa. When the diagnosis is suspected, bronchoscopic biopsy should be avoided as it might lead to fatal hemorrhage. Selective bronchial artery embolization can stop the bleeding, but surgery can be required.
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spelling pubmed-103186702023-07-05 Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature Daboussi, Salsabil kacem, Marwa Boubaker, Nouha Chaabene, Mariem Aichaouia, Chiraz Mhamdi, Samira Moatemri, Zied J Cardiothorac Surg Case Report BACKGROUND: Dieulafoy’s disease of the bronchus can cause massive and even fatal hemoptysis. Even though it is rare, it should be considered by physicians all over the world. This paper reports a case of bronchial Dieulafoy’s disease and summarizes the data of similar cases reported in literature. METHODS: We report a case of bronchial Dieulafoy’s disease (BDD) in Tunisia. We also present a review of literature related to BDD from 1995 to 2022 using the PubMed, Google Scholar, web of science and Chinese National Knowledge Infrastructure Databases. Clinical characteristics, chest imaging, bronchoscopic and angiographic findings were summarized. Treatment courses were identified as well as patients’ outcome. RESULTS: We report the case of a 41-year-old man, so far in good health, presenting with massive hemoptysis. Bronchoscopy showed blood clots and a protruding lesion covered by mucosa with a white pointed cap at the entrance of the right upper lobe. Biopsies were not attempted. Embolization of bronchial artery was first realized and was not successful, with post procedure complications. Surgical intervention stopped the bleeding and pathological examination of the resected specimen confirmed Dieulafoy’s disease of the bronchus. Ninety cases of BDD were reported from 1995 to 2022. The main symptom was hemoptysis. Chest imaging findings were not specific. The diagnosis of BDD was mainly based on the bronchoscopy, branchial angiography and pathological findings or surgical specimens. Bronchoscopy findings were mostly nodular or prominent lesions (52.4%). Twenty-eight patients underwent bronchoscopic biopsies, 20 had massive bleeding and 10 died. Bronchial angiography mainly showed tortuous and dilation of bronchial artery, and the lesions were mainly located in the right bronchus. Selective bronchial artery embolization (SBAE) was performed in 32 patients and 39 patients underwent surgery. CONCLUSION: To our knowledge, this is the first case of bronchial Dieulafoy’s disease to be reported in Tunisia and North Africa. When the diagnosis is suspected, bronchoscopic biopsy should be avoided as it might lead to fatal hemorrhage. Selective bronchial artery embolization can stop the bleeding, but surgery can be required. BioMed Central 2023-07-04 /pmc/articles/PMC10318670/ /pubmed/37403165 http://dx.doi.org/10.1186/s13019-023-02242-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Daboussi, Salsabil
kacem, Marwa
Boubaker, Nouha
Chaabene, Mariem
Aichaouia, Chiraz
Mhamdi, Samira
Moatemri, Zied
Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title_full Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title_fullStr Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title_full_unstemmed Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title_short Dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
title_sort dieulafoy’s disease of the bronchus: rare but potentially fatal: a case report and a review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318670/
https://www.ncbi.nlm.nih.gov/pubmed/37403165
http://dx.doi.org/10.1186/s13019-023-02242-0
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