
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Thoracic aortic aneurysm causes
Introduction
Overview
Overview
Two of the most common causes of thoracic aorta aneurysm are Marfan’s syndrome and atherosclerosis. In some centers, a prior history of dissection with aneurysmal dilation is the most common cause of surgical repair.
Causes
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
Causes by Organ System
| Cardiovascular | Aortic dissection, aortic stenosis, aortic valve replacement, aortitis, atherosclerosis, bacterial endocarditis, bicuspid aortic valve, systemic hypertension |
| Chemical / poisoning | No underlying causes |
| Dermatologic | No underlying causes |
| Drug Side Effect | No underlying causes |
| Ear Nose Throat | No underlying causes |
| Endocrine | No underlying causes |
| Environmental | No underlying causes |
| Gastroenterologic | No underlying causes |
| Genetic | Arterial tortuosity syndrome, bicuspid aortic valve, Ehlers-Danlos syndrome, familial thoracic aortic aneurysms and dissections, Loeys-Dietz syndrome, Marfan syndrome, Turner syndrome |
| Hematologic | No underlying causes |
| Iatrogenic | Previous surgery on the aorta |
| Infectious Disease | Aortitis, quaternary syphilis, septic embolism |
| Musculoskeletal / Ortho | No underlying causes |
| Neurologic | No underlying causes |
| Nutritional / Metabolic | No underlying causes |
| Obstetric/Gynecologic | No underlying causes |
| Oncologic | No underlying causes |
| Opthalmologic | No underlying causes |
| Overdose / Toxicity | No underlying causes |
| Psychiatric | No underlying causes |
| Pulmonary | Wegener’s granulomatosis |
| Renal / Electrolyte | No underlying causes |
| Rheum / Immune / Allergy | Ankylosing spondylitis, aortitis, Behcet’s disease, giant cell arteritis, reactive arthritis, rheumatoid arthritis, rheumatoid vasculitis, Takayasu’s arteritis, Wegener’s granulomatosis |
| Sexual | No underlying causes |
| Trauma | Sudden deceleration |
| Urologic | No underlying causes |
| Miscellaneous | No underlying causes |
Causes in Alphabetical Order
- Ankylosing spondylitis
- Aortic dissection
- Aortic stenosis
- Aortitis
- Aortic valve replacement
- Arterial tortuosity syndrome
- Atherosclerosis
- Bacterial infection, often following valvular endocarditis
- Behcet’s disease
- Bicuspid aortic valve
- Ehlers-Danlos syndrome
- Familial thoracic aortic aneurysms and dissections
- Giant cell arteritis
- Loeys-Dietz syndrome
- Marfan’s syndrome
- Quaternary syphilis
- Reactive arthritis
- Rheumatoid arthritis
- Rheumatoid vasculitis
- Septic embolism
- Systemic hypertension
- Takayasu’s arteritis
- Temporal arteritis
- Traumatic – Sudden deceleration
- Turner’s syndrome
- Wegener’s granulomatosis
Causes Based Upon Inherited versus Sporadic versus Syndromic Basis
Causes Based Upon Inherited versus Sporadic versus Syndromic Basis
Sporadic Causes
- Ankylosing spondylitis
- Atherosclerosis
- Bacterial infection, often following valvular endocarditis
- Behcet’s disease[4]
- Giant cell arteritis[5]
- Previous injury to the aorta such as an aortic dissection
- Syphilis[6]
- Takayasu’s arteritis[7]
- Traumatic – sudden deceleration
Familial Causes
- Familial thoracic aortic aneurysms and dissections[8]
- Bicuspid aortic valve with post-stenotic dilation due to turbulence[9]
Syndromic Causes
- Marfan’s syndrome: Aortic root dilation with or without associated aortic regurgitation occurs in 75%-80% of marfan’s patients[10].
- Loeys-Dietz syndrome[11]
- Ehlers-Danlos syndrome
- Turner’s syndrome[12]
References
References
- ↑ Cheung K, Boodhwani M, Chan KL, Beauchesne L, Dick A, Coutinho T (February 2017). “Thoracic Aortic Aneurysm Growth: Role of Sex and Aneurysm Etiology”. J Am Heart Assoc. 6 (2). doi:10.1161/JAHA.116.003792. PMC 5523737. PMID 28159818.
- ↑ Naidu DP, Quinones JA, Lutschg KW, Balaguru D (August 2017). “Healthy Adolescent with a Mycotic Aortic Aneurysm from Community-Acquired Methicillin-Resistant Staphylococcus aureus”. Tex Heart Inst J. 44 (4): 279–282. doi:10.14503/THIJ-16-5932. PMC 5577956. PMID 28878584.
- ↑ Im KS, Choi MK, Jeon YK, Lee JM (July 2016). “Dissecting thoracic aortic aneurysm associated with tuberculous pleural effusion”. J Thorac Dis. 8 (7): E520–2. doi:10.21037/jtd.2016.05.68. PMC 4958844. PMID 27499987.
- ↑ Zhang SH, Zhang FX (September 2017). “Behcet’s disease with recurrent thoracic aortic aneurysm combined with femoral artery aneurysm: a case report and literature review”. J Cardiothorac Surg. 12 (1): 79. doi:10.1186/s13019-017-0644-y. PMC 5585960. PMID 28874203.
- ↑ Kermani TA, Warrington KJ, Crowson CS, Ytterberg SR, Hunder GG, Gabriel SE, Matteson EL (December 2013). “Large-vessel involvement in giant cell arteritis: a population-based cohort study of the incidence-trends and prognosis”. Ann. Rheum. Dis. 72 (12): 1989–94. doi:10.1136/annrheumdis-2012-202408. PMC 4112513. PMID 23253927.
- ↑ Li W, Yin XJ, Liu HY, Yang R (2016). “Syphilitic aortic aneurysm with a pulmonary lesion: a case report and literature view”. Springerplus. 5 (1): 1725. doi:10.1186/s40064-016-3397-5. PMC 5053956. PMID 27777861.
- ↑ Pan L, Du J, Chen D, Zhao Y, Guo X, Qi G, Wang T, Du J (October 2019). “Takayasu Arteritis with Dyslipidemia Increases Risk of Aneurysm”. Sci Rep. 9 (1): 14083. doi:10.1038/s41598-019-50527-z. PMC 6773689 Check
|pmc=value (help). PMID 31575993. - ↑ Isselbacher EM, Lino Cardenas CL, Lindsay ME (June 2016). “Hereditary Influence in Thoracic Aortic Aneurysm and Dissection”. Circulation. 133 (24): 2516–28. doi:10.1161/CIRCULATIONAHA.116.009762. PMC 5031368. PMID 27297344.
- ↑ Norton E, Yang B (2017). “Managing Thoracic Aortic Aneurysm in Patients with Bicuspid Aortic Valve Based on Aortic Root-Involvement”. Front Physiol. 8: 397. doi:10.3389/fphys.2017.00397. PMC 5469203. PMID 28659818.
- ↑ Pepe G, Giusti B, Sticchi E, Abbate R, Gensini GF, Nistri S (2016). “Marfan syndrome: current perspectives”. Appl Clin Genet. 9: 55–65. doi:10.2147/TACG.S96233. PMC 4869846. PMID 27274304.
- ↑ MacFarlane EG, Parker SJ, Shin JY, Kang BE, Ziegler SG, Creamer TJ, Bagirzadeh R, Bedja D, Chen Y, Calderon JF, Weissler K, Frischmeyer-Guerrerio PA, Lindsay ME, Habashi JP, Dietz HC (February 2019). “Lineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome”. J. Clin. Invest. 129 (2): 659–675. doi:10.1172/JCI123547. PMC 6355234. PMID 30614814.
- ↑ Corbitt H, Morris SA, Gravholt CH, Mortensen KH, Tippner-Hedges R, Silberbach M, Maslen CL (October 2018). “TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome”. PLoS Genet. 14 (10): e1007692. doi:10.1371/journal.pgen.1007692. PMC 6188895. PMID 30281655.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2] Mohammed Salih, MD. [3]
