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Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report
BACKGROUND: Pulmonary artery aneurysms constitute <1% of aneurysms occurring in the thoracic cavity. Congenital cardiac defects are responsible for the majority (>50%) of cases, however, pulmonary artery aneurysm is a rare sequelae of pulmonary tuberculosis reported in about 5% of patients wit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516347/ https://www.ncbi.nlm.nih.gov/pubmed/28720136 http://dx.doi.org/10.1186/s13256-017-1360-x |
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author | Pallangyo, Pedro Lyimo, Frederick Bhalia, Smita Makungu, Hilda Nyangasa, Bashir Lwakatare, Flora Suranyi, Pal Janabi, Mohamed |
author_facet | Pallangyo, Pedro Lyimo, Frederick Bhalia, Smita Makungu, Hilda Nyangasa, Bashir Lwakatare, Flora Suranyi, Pal Janabi, Mohamed |
author_sort | Pallangyo, Pedro |
collection | PubMed |
description | BACKGROUND: Pulmonary artery aneurysms constitute <1% of aneurysms occurring in the thoracic cavity. Congenital cardiac defects are responsible for the majority (>50%) of cases, however, pulmonary artery aneurysm is a rare sequelae of pulmonary tuberculosis reported in about 5% of patients with chronic cavitary tuberculosis on autopsy. The natural history of this potentially fatal condition remains poorly understood and guidelines for optimal management are controversial. CASE PRESENTATION: A 24-year-old man, a nursing student of African descent, was referred to us from an up-country regional hospital with a 4-week history of recurrent episodes of breathlessness, awareness of heartbeats and coughing blood 3 weeks after completing a 6-month course of anti-tuberculosis drugs. A physical examination revealed conjuctival and palmar pallor but there were no stigmata of connective tissue disorders, systemic vasculitides or congenital heart disease. An examination of the cardiovascular system revealed accentuated second heart sound (S(2)) with early diastolic (grade 1/6) and holosystolic (grade 2/6) murmurs at the pulmonic and tricuspid areas respectively. Blood tests showed iron deficiency anemia, prolonged bleeding time, and mild hyponatremia. A chest radiograph revealed bilateral ovoid-shaped perihilar opacities while a computed tomography scan showed bilateral multiple pulmonary artery pseudoaneurysms with surrounding hematoma together with adjacent cystic changes, consolidations, and tree-in-bud appearance. Our patient refused to undergo surgery and died of aneurismal rupture after 9 days of hospitalization. CONCLUSIONS: The presence of intractable hemoptysis among patients with tuberculosis even after completion of anti-tuberculosis course should raise an index of suspicion for pulmonary artery aneurysm. Furthermore, despite of its rarity, early recognition and timely surgical intervention of pulmonary artery aneurysm is crucial to reducing morbidity and preventing the attributed mortality. |
format | Online Article Text |
id | pubmed-5516347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55163472017-07-20 Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report Pallangyo, Pedro Lyimo, Frederick Bhalia, Smita Makungu, Hilda Nyangasa, Bashir Lwakatare, Flora Suranyi, Pal Janabi, Mohamed J Med Case Rep Case Report BACKGROUND: Pulmonary artery aneurysms constitute <1% of aneurysms occurring in the thoracic cavity. Congenital cardiac defects are responsible for the majority (>50%) of cases, however, pulmonary artery aneurysm is a rare sequelae of pulmonary tuberculosis reported in about 5% of patients with chronic cavitary tuberculosis on autopsy. The natural history of this potentially fatal condition remains poorly understood and guidelines for optimal management are controversial. CASE PRESENTATION: A 24-year-old man, a nursing student of African descent, was referred to us from an up-country regional hospital with a 4-week history of recurrent episodes of breathlessness, awareness of heartbeats and coughing blood 3 weeks after completing a 6-month course of anti-tuberculosis drugs. A physical examination revealed conjuctival and palmar pallor but there were no stigmata of connective tissue disorders, systemic vasculitides or congenital heart disease. An examination of the cardiovascular system revealed accentuated second heart sound (S(2)) with early diastolic (grade 1/6) and holosystolic (grade 2/6) murmurs at the pulmonic and tricuspid areas respectively. Blood tests showed iron deficiency anemia, prolonged bleeding time, and mild hyponatremia. A chest radiograph revealed bilateral ovoid-shaped perihilar opacities while a computed tomography scan showed bilateral multiple pulmonary artery pseudoaneurysms with surrounding hematoma together with adjacent cystic changes, consolidations, and tree-in-bud appearance. Our patient refused to undergo surgery and died of aneurismal rupture after 9 days of hospitalization. CONCLUSIONS: The presence of intractable hemoptysis among patients with tuberculosis even after completion of anti-tuberculosis course should raise an index of suspicion for pulmonary artery aneurysm. Furthermore, despite of its rarity, early recognition and timely surgical intervention of pulmonary artery aneurysm is crucial to reducing morbidity and preventing the attributed mortality. BioMed Central 2017-07-19 /pmc/articles/PMC5516347/ /pubmed/28720136 http://dx.doi.org/10.1186/s13256-017-1360-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Pallangyo, Pedro Lyimo, Frederick Bhalia, Smita Makungu, Hilda Nyangasa, Bashir Lwakatare, Flora Suranyi, Pal Janabi, Mohamed Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title | Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title_full | Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title_fullStr | Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title_full_unstemmed | Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title_short | Bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
title_sort | bilateral multiple pulmonary artery aneurysms associated with cavitary pulmonary tuberculosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516347/ https://www.ncbi.nlm.nih.gov/pubmed/28720136 http://dx.doi.org/10.1186/s13256-017-1360-x |
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