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February 6, 2026BMJ Case Reports0 citations

Angioinvasive pulmonary mucormycosis presenting with massive haemoptysis secondary to pulmonary artery pseudoaneurysm

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SKSourabh prakash KulkarniVBVenkatraman BhatGKGA Karthik

Key Points

  • To highlight the implications of angioinvasive mucormycosis as a rare cause of pulmonary artery pseudoaneurysm.
  • Presented a case of pulmonary mucormycosis leading to massive haemoptysis.
  • Emphasized the need for clinical suspicion and appropriate imaging.
  • Outlined the management approach that led to successful intervention.
  • Timely identification of the cause prevented a potentially fatal outcome.
  • Improved imaging techniques facilitated accurate diagnosis.
  • Overall management resulted in resolution of the pulmonary artery pseudoaneurysm.

Abstract

Pulmonary artery pseudoaneurysm (PAP) is a rare but potentially fatal entity caused by a variety of underlying conditions. They may be congenital in origin or occur due to infective complications or occasionally secondary to pulmonary arterial hypertension. Among infective processes, tuberculosis and bacterial infections are the most common causative agents. There are few isolated reports of angio-invasive mucormycosis causing PAP; many of them were detected postmortem. Diagnosis of specific aetiology is often overlooked due to lack of clinical suspicion, as a result of incomplete investigations or due to inappropriate imaging. This report presents a case of pulmonary mucormycosis complicated by PAP in a patient with clinically unsuspected, uncontrolled diabetes. We highlight how the combination of heightened clinical suspicion, appropriate imaging and timely intervention helped us to treat a potentially fatal complication in our patient.

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Cite This Study

Kulkarni et al. (2026) studied this question.

synapsesocial.com/papers/698586498f7c464f2300a54chttps://doi.org/10.1136/bcr-2025-269672
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