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Uncommon Cause of Internal Mammary Artery Pseudoaneurysm.

Authors :
Prasad, Rohan M.
Liu, Jason Z.
Garces, Christopher
Duwadi, Ayushma
Choi, James
Anwar, Farah
Olomu, Adesuwa
Source :
Ochsner Journal. Sep2022, Vol. 22 Issue 3, p244-248. 5p.
Publication Year :
2022

Abstract

Background: Internal mammary artery pseudoaneurysms most commonly develop from thoracic penetrating trauma or procedures. However, other important etiologies should not be overlooked. Case Report: A 27-year-old female presentedwith antiphospholipid antibody syndrome, thrombotic microangiopathy, end-stage renal disease on hemodialysis, and epilepsy. On admission, the patient had pulseless electrical activity and hypertensive emergency. After the patientwas successfully resuscitated, she developed status epilepticus. Laboratoryworkup on admission revealed a subtherapeutic international normalized ratio, elevated C-reactive protein and sedimentation rate, and acute anemia. Imaging showed a right-sided subdural hematoma with amidline shift and likely internal mammary artery pseudoaneurysm. Angiography demonstrated aneurysmal dilation, segmental narrowing, and a string of beads appearance. Because of our patient's demographics, string of beads appearance on diagnostic angiography, history of renal disease, and negative hepatitis serology, fibromuscular dysplasia was considered the etiology of the internal mammary artery pseudoaneurysm. The family opted for 2 burr holes and a subdural drain but declined further diagnostic and therapeutic interventions because of anoxic brain injury and poor prognosis. Conclusion: In this patient, the etiology of the internal mammary artery pseudoaneurysm was attributed to fibromuscular dysplasia. Although this patient's family chose comfortmeasures, treatmentmethods are available for internal mammary artery pseudoaneurysms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15245012
Volume :
22
Issue :
3
Database :
Academic Search Index
Journal :
Ochsner Journal
Publication Type :
Academic Journal
Accession number :
159207317
Full Text :
https://doi.org/10.31486/toj.21.0090