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Tissue plasminogen activator associated pulmonary hemorrhage in patient with ACTA2-associated arteriopathy
Travis G Hughes1, Mark A Wurth2, Mary B Sheppard3,4,5
1Division of Vascular and Endovascular Surgery, University of Kentucky, Lexington, KY.
Abstract:
Pulmonary hemorrhage after administration of tissue plasminogen activator (tPA) is a rare complication. We present a 15-year-old boy with a heterozygous pathogenic variant in ACTA2 who presented with right brachial artery aneurysm thrombosis treated initially with tPA, resulting in pulmonary hemorrhage. We hypothesize that the underlying pulmonary abnormalities caused by the pathogenic ACTA2 variant may be a risk factor for pulmonary hemorrhage after tPA administration.
Insights
A rare complication, pulmonary hemorrhage, occurred after tissue plasminogen activator (tPA) treatment in a boy with an ACTA2 gene variant. This suggests ACTA2 variants may increase risk for tPA-related pulmonary bleeding.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Pulmonology
Background:
- Tissue plasminogen activator (tPA) is a thrombolytic agent used to treat thrombotic events.
- Rarely, tPA administration can lead to serious complications such as pulmonary hemorrhage.
- Genetic factors may influence the risk of adverse events following tPA therapy.
Observation:
- A 15-year-old male presented with thrombosis of a right brachial artery aneurysm.
- The patient received tPA for treatment of the arterial thrombosis.
- Following tPA administration, the patient developed pulmonary hemorrhage.
Findings:
- The patient was found to have a heterozygous pathogenic variant in the ACTA2 gene.
- The ACTA2 gene is associated with vascular abnormalities.
- Pulmonary hemorrhage occurred subsequent to tPA treatment in this patient with an ACTA2 variant.
Implications:
- Pathogenic variants in ACTA2 may predispose individuals to pulmonary hemorrhage after tPA administration.
- Underlying pulmonary abnormalities associated with ACTA2 variants could be a risk factor.
- Further research is warranted to elucidate the relationship between ACTA2 variants and tPA-induced pulmonary bleeding.
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