|IMAGES IN CLINICAL MEDICINE
|Year : 2017 | Volume
| Issue : 3 | Page : 183-184
Stanford type B aortic dissection in an elderly patient with silent aortic coarctation
Choon-Bing Chua1, Chih-Wei Hsu1, Hsuan-Yin Wu2, Chao-Sheng Chang1, Kuo-Hsin Lee1
1 Department of Emergency Medicine, E-Da Hospital and I-Shou University, Kaohsiung, Taiwan
2 Division of Cardiovascular Surgery, Department of Surgery, E-Da Hospital and I-Shou University, Kaohsiung, Taiwan
|Date of Submission||25-Nov-2016|
|Date of Decision||12-Dec-2016|
|Date of Acceptance||16-Feb-2017|
|Date of Web Publication||14-Sep-2017|
Department of Emergency Medicine, E-Da Hospital, 1, Yi-Da Road, Jiao-Su Village, Yan-Chao District, Kaohsiung
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Chua CB, Hsu CW, Wu HY, Chang CS, Lee KH. Stanford type B aortic dissection in an elderly patient with silent aortic coarctation. Tzu Chi Med J 2017;29:183-4
|How to cite this URL:|
Chua CB, Hsu CW, Wu HY, Chang CS, Lee KH. Stanford type B aortic dissection in an elderly patient with silent aortic coarctation. Tzu Chi Med J [serial online] 2017 [cited 2022 May 24];29:183-4. Available from: https://www.tcmjmed.com/text.asp?2017/29/3/183/214702
A 64-year-old man presented to our emergency department with sudden onset of severe back pain 1 h ago. He had been physically well without history of hypertension or other systemic diseases. On physical examination, a significant difference between blood pressure in the upper and lower limbs was noticed (183/93 and 183/99 mmHg in the right and left upper extremity; 148/98 and 163/104 mmHg in the right and left lower extremity, respectively). Chest radiography showed a prominent aortic knob. Chest computed tomography revealed a Stanford type B aortic dissection associated with an aortic coarctation and persistent left superior vena cava [Figure 1]. Furthermore, the coarctation was found to coexist with tubular arch hypoplasia [Figure 2] and [Figure 3]. Considering the extreme age and high risk for surgery, medical treatment with angiotensin receptor blocker was given. The patient was in good physical condition after a 6-month follow-up.
|Figure 1: Contrast-enhanced coronal computed tomography image demonstrates the persistent left superior vena cava (white arrows) and the coarctation connecting from the tubular arch hypoplasia (white arrowhead)|
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|Figure 2: Three-dimensional reconstruction of a computed tomography angiography. (a) Anterior view shows a Stanford type B aortic dissection (black arrowhead) with obvious anomaly of aortic arch. The aortic arch is seemingly interrupted in the middle and divided into proximal and distal portion after bifurcation of left subclavian artery (white arrow). The distal portion of the arch enlarges to a bulbous aneurysm. (b) Posterior view demonstrates a downward curving tubular hypoplasia (white arrowhead) which arises from the proximal portion of the aortic arch and funnels down toward the discrete coarctation (black arrow). The dissection shows the intimal flap originated from the distal portion of aortic arch (black arrowhead)|
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|Figure 3: Contrast-enhanced transaxial computed tomography image demonstrates the aortic dissection started just after the discrete coarctation that was connected from the tubular hypoplasia (white arrowhead). There were collateral vessels of dilated internal mammary arteries (white arrows) and intercostal artery (black arrow). pAo: Proximal portion of aortic arch, dAo: Distal portion of aortic arch|
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Aortic coarctation is an uncommon congenital luminal narrowing of the aortic arch which is commonly associated with cardiovascular abnormalities. Moreover, the persistent left superior vena cava is a rare vascular anomaly which is most commonly seen in isolation and could also be associated with coarctation of aorta . By morphology, aortic coarctation is divided into two main types: discrete coarctation and tubular arch hypoplasia. These two types may coexist . The average survival age of unrepaired aortic coarctation was 35 years of age with high mortality in advanced age. Without correction, coarctation resulted in high morbidity and mortality from hypertension, coronary heart disease, aortic dissection, heart failure, aortic rupture, and infective endarteritis .
Aortic dissection, especially type B, is rarely associated with coarctation. To the best of our knowledge, only 13 cases of aortic coarctation with type B dissection were reported with patients' ages ranging from 25 to 56 years ,,,,,,,,,,,,. The locations of coarctations were mostly distal to the left subclavian artery except one which was located between left carotid and subclavian arteries . All the reported coarctations were discrete coarctations. Our case is unique not only of its extreme age but also of its discrete coarctation coexisting with tubular arch hypoplasia and persistent left superior vena cava.
Although uncomplicated type B dissection is well established to be treated conservatively, adult aortic coarctation is still considered a surgical candidate in the presence of peak-to-peak coarctation gradient >20 mmHg. The treatment for aortic coarctation included surgical repair, balloon angioplasty, and stenting . While balloon angioplasty is the preferred treatment for discrete coarctation in infants and children between 4 months and 5 years of age (<25 kg), stenting is the first choice for larger patients (>25 kg). In the presence of complex coarctation anatomy such as arch hypoplasia, the decision to use balloon angioplasty or stenting versus surgical approach is made on a case-by-case basis. However, for the elderly concerning about the tissue integrity of the paracoarctation region with subsequent risk from complications of interventions, continued medical therapy with goal of controlling pressure gradient using beta-blocker, angiotensin-converting enzyme inhibitors, or angiotensin receptor inhibitors may be an acceptable option .
Declaration of patient consent
The authors certify that the patient have obtained appropriate patient consent form. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that his name and initial will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]