Case Report
A rare case of intercostal-to-pulmonary artery fistula and its endovascular treatment in the setting of post pulmonary tuberculosis bronchiectasis and haemoptysis
Submitted: 19 February 2025 | Published: 20 June 2025
About the author(s)
Lwandile Majozini, Department of Radiology, Faculty of Health Sciences, School of Clinical Medicine, University of the Witwatersrand, Johannesburg, South AfricaWinile Nkosi, Department of Radiology, Faculty of Health Sciences, School of Clinical Medicine, University of the Witwatersrand, Johannesburg, South Africa
Abstract
Intercostal artery-to-pulmonary artery fistula is an extremely rare variant of systemic artery-to-pulmonary artery fistulas (SA-PAFs). A case of a 38-year-old man presenting with clinically significant haemoptysis secondary to an intercostal artery-to-pulmonary artery fistula in the setting of post-pulmonary tuberculosis (TB) bronchiectasis is described. The fistulae were successfully treated with endovascular coils.
Contribution: This case report illustrates an intercostal artery-to-pulmonary artery fistula associated with post-primary tuberculosis bronchiectasis, highlighting its multimodal radiological features and successful endovascular treatment.
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