A giant left internal iliac artery aneurysm in a patient with Loeys-Dietz syndrome.
Ivan I SkopinValerii S ArakelyanNickolai A TchurikovAndrei M BelyaevPublished in: Interactive cardiovascular and thoracic surgery (2021)
A 16-year-old female presented with left iliac fossa pain. In January 2021, she was admitted to her local hospital with severe lower abdominal pain and the pelvic ultrasound demonstrated a 13-cm left internal iliac artery dissecting aneurysm with its partial thrombosis. On examination, she had a high-arched palate, multiple skin stretch marks, flat feet and a soft systolic ejection murmur at the left 5th mid-clavicular line. She had a mildly tender abdomen in the left iliac fossa. Computed tomography angiography demonstrated a 12.2 cm × 10.4 cm × 12.5 cm left internal iliac artery aneurysm. During surgery, the aneurysm was incised and the proximal and distal orifices of the internal iliac artery were ligated. Genetic testing yielded 2 mutations in the SMAD3 gene characteristic for Loeys-Dietz syndrome.
Keyphrases
- coronary artery
- endovascular treatment
- minimally invasive
- case report
- heart failure
- healthcare
- pain management
- chronic pain
- blood pressure
- gene expression
- magnetic resonance
- left ventricular
- abdominal aortic aneurysm
- emergency department
- dna methylation
- percutaneous coronary intervention
- early onset
- pulmonary embolism
- rectal cancer
- copy number
- transforming growth factor
- transcription factor
- wound healing
- acute coronary syndrome