Takayasu arteritis with coronary aneurysms causing acute myocardial infarction in a young man

Sana Ouali1, Slim Kacem, Fatma Ben Fradj

  • 1Department of Cardiology, Sahloul Hospital, Sousse 5054, Tunisia. sanaouali@hotmail.fr

Insights

Takayasu arteritis, a rare inflammatory condition, presented unusually in a young man with myocardial infarction and complete heart block due to a coronary artery aneurysm. This case highlights a unique combination of vascular complications and emphasizes differential diagnosis considerations.

Area of Science:

  • Cardiology
  • Vascular Inflammation
  • Rheumatology

Background:

  • Takayasu arteritis typically affects young women, involving the aorta and its branches.
  • It is characterized by large-vessel inflammation and stenosis, occlusion, or aneurysms.

Observation:

  • A rare case of Takayasu arteritis in a 19-year-old man presenting with acute inferior myocardial infarction and complete atrioventricular block.
  • The patient exhibited a giant aneurysm in the right coronary artery causing occlusion, alongside aneurysmal dilations in carotid, vertebral, and renal arteries.

Findings:

  • Successful medical management with corticosteroids improved coronary blood flow.
  • Percutaneous transluminal angioplasty addressed associated renal artery stenosis, resolving renovascular hypertension.
  • The patient remained stable with no cardiovascular complications during 12 months of follow-up.

Implications:

  • This case presents a previously unreported association of Takayasu arteritis with myocardial infarction, complete heart block, and multiple arterial aneurysms.
  • It underscores the importance of considering Takayasu arteritis in the differential diagnosis of young patients with complex cardiovascular and renovascular presentations.
  • The successful management highlights a multimodal therapeutic approach involving medical and interventional strategies.

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