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| 2013, Volume 28, Number 1, Page(s) 047-050 | |||||||||
| [ Summary ] [ PDF ] [ Similar Articles ] [ Mail to Author ] [ Mail to Editor ] | |||||||||
| Left Main Coronary Dissection in a Patient with Takayasu's Arteritis | |||||||||
| DOI: 10.5606/tjr.2013.2676 | |||||||||
| İbrahim AKPINAR,1 Muhammet Raşit SAYIN,1 Turgut KARABAĞ,1 Emrah KÜÇÜK,1 Sait Mesut DOĞAN,1 Mustafa BÜYÜKATEŞ,2 Mustafa AYDIN1 | |||||||||
| 1Department of Cardiology, Medical Faculty of Bülent Ecevit University, Zonguldak, Turkey 2Department of Cardiovascular Surgery, Medical Faculty of Bülent Ecevit University, Zonguldak, Turkey |
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| Keywords: Arteritis; coronary; dissection; Takayasu's | |||||||||
| Abstract | |||||||||
Takayasu's arteritis is a type of vasculitis which is
characterized by chronic inflammation involving the aorta
and its major proximal branches. The inflammatory process
in the vessel wall due to intimal thickening and fibrosis may
result in catastrophic events such as vascular stenosis
and spontaneous dissection. However, spontaneous
coronary dissection is a relatively rare outcome. The
use of transthoracic echocardiography in the evaluation
of thoracic aortic involvement has been shown to be
advantageous since this method is relatively cheap and
non-invasive. In this article, we report a 48-year-old female
case who was previously diagnosed with Takayasu's
arteritis with a spontaneous left main coronary artery
dissection which was detected by coronary angiography
following the sudden onset of severe chest pain. |
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| Introduction | |||||||||
Takayasu's arteritis, which was first diagnosed by a
Japanese ophthalmologist in 1908 based on ocular
findings,1 is characterized by organ ischemia as a
result of chronic inflammation of the aorta and its
main branches. Takayasu's arteritis predominantly
occurs before the age of 40 and is more common
in females. Coronary involvement, although rare, is
often ostial and causes ischemia due to inflammatory
stenosis. In addition to coronary stenosis, late-term
vital complications, such as vascular dissection, should
be monitored carefully. Furthermore, transthoracic
echocardiography should be considered as an alternative non-invasive method to be used in the follow-up and
evaluation of the thoracic aorta. |
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| Case Presentation | |||||||||
A 48-year-old female patient with no known
cardiovascular risk factors was referred to our
emergency department due to the sudden onset of
severe, constricting chest pain that had been occurring
for the previous four hours. On physical examination,
blood pressure measurements from the right and left
arms were 155/90 and 130/80 mmHg, respectively,
and an apical 2/6 systolic heart murmur was heard. Electrocardiography (ECG) showed a 1 mm ST-segment
depression in the precordial derivation and a 1.5
mm ST elevation in augmented vector right (aVR)
(Figure 1). Laboratory tests revealed a creatinine level
of 1.8 mg/dL, a urea level of 80 mg/dL, and slightly
increased troponin/creatine kinase-MB fraction (CKMB)
levels. Based on the patient's medical history, she
had been diagnosed with Takayasu's arteritis 12 years
earlier due to renal artery stenosis, subclavian artery
stenosis, and intermittent claudication. In addition,
a pulmonary embolism had been detected four years
previously. Transthoracic echocardiography showed
normal left ventricular systolic function, mild aortic
regurgitation, and moderate tricuspid regurgitation.
The systolic pulmonary artery pressure was 35 mmHg.
The ascending aorta was measured as 4.0 cm, and no
dissection flap was detected. An echocardiographic
examination revealed that the proximal aorta was
thickened and hyperechogenic, and calcific plaques
were commonly observed on the inner surface of
the lumen (Figure 2). Using suprasternal imaging,
it was determined that the arcus aorta was 4.3 cm
in width, and moderate proximal brachiocephalic,
common carotid, and subclavian artery stenoses were
detected. Thickening of the arcus aorta wall was
observed in addition to an increased echogenic area
and a rough inner lumen (Figure 3). Due to ongoing
severe chest pain, the patient was urgently transferred
to the catheter laboratory. Spontaneous dissection
causing severe stenosis in the proximal left main
coronary artery (LMCA) was detected by coronary
angiography (Figure 4), but all other coronary vessels
were normal. In addition, there was no significant
narrowing observed on the carotid Doppler ultrasound.
The patient's hemodynamic values were normal, and
an emergency operation was planned. Ascending
aorta, upper, and lower vena cava cannulations were performed after a median sternotomy and then the
patient entered into the pump. The heart was stopped
by cold potassium while the patient was under general
(rectal temperature 28 °C) and topical hypothermia.
During an intraoperative evaluation of the thoracic
aorta, it was noted that it was completely calcified and
hardened. Aortocoronary anastomosis was performed
using a saphenous venous graft because of the ostial
involvement of the subclavian and left internal
mammary arteries (LIMA). The postoperative course
was uneventful, and the patient was discharged on
postoperative day 10.
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| Discussion | |||||||||
Takayasu's arteritis, also known as Martorell's
syndrome, is an inflammatory disease that often
affects the aorta and the proximal segments of the
main aortic. It also may result in vascular occlusion
due to intimal fibrosis and thickening. In addition to ostial stenosis, aorta aneurysms may be encountered,
depending on the existence panarteritis. This is
especially true if there is destruction of the tunica media. The cause of Takayasu's arteritis is not yet
known, but it is more common in young females.
Symptoms vary depending on the involvement and
severity of the functional impairment of the organs
supplied by the stenotic vessels. During the early stage,
rheumatic complaints such as fever, malaise, fatigue,
general body pain, and weight loss may occur due to
the systemic inflammatory condition. As a result of
chronic vascular inflammation, intimal fibrosis may
result in catastrophic outcomes, such as organ ischemia.
Arm and leg pain, renovascular hypertension, and
neurological symptoms may develop in patients during
advanced stages of this disease. Pulmonary arterial
hypertension and emboli are also often observed due to
the involvement of the pulmonary artery. A diagnosis
of Takayasu's arteritis is made clinically according to
the presence of at least three of the American College of
Rheumatology (ACR) 1990 criteria:2 (i) disease onset
prior to age 40, (ii) claudication of the extremities,
(iii) reduction in the brachial pulse, (iv) more than a
10 mmHg pressure difference between the two arms,
(v) detection of a murmur around the aorta, subclavian
artery, or both, and (vi) abnormal arterial imaging.
There are no specific blood tests for Takayasu's arteritis. Medical treatments include immunosuppressive
therapy, such as steroids, cyclophosphamide, and
methotrexate, but there is no current agreement on the
best treatment option. Coronary artery involvement
occurs in 5-15% of patients. Although Takayasu's
arteritis often causes ostial stenosis, spontaneous
LMCA dissection is an extremely rare complication.3
In the case of sudden-onset chest pain in a patient with
this disease, coronary artery dissection should be
considered due to the need for early diagnosis and
rapid treatment. However, dissection of the ascending
aorta should be excluded. In our patient, transthoracic
echocardiography (suprasternal view) did not show
aortic dissection. Therefore, computed tomography
(CT) and magnetic resonance imaging (MRI) were
not performed because of poor renal function. An
echocardiographic examination should be used during
routine follow-up of all patients with Takayasu's
arteritis to evaluate aortic involvement. Transthoracic
echocardiography is non-invasive and inexpensive and
has been proven to be an excellent method for patient
diagnosis and follow-up. Intimal thickening and
hyperechogenic appearance due to calcification of the
aorta and its major branches are important and valuable
observations. As in our patient, echocardiography
may be useful as an alternative to MRI and CT
for detecting ostial stenosis of the main branches.
Percutaneous coronary intervention (PCI) for left main
coronary stenosis has been described in the literature;
however, invasive treatments should be decided upon
according to the lesion location, number of stenotic
vessels, and available technical equipment.4 There are
currently no clinical studies showing the superiority
of percutaneous intervention over surgical therapy in
patients with Takayasu's arteritis complicated by left
main coronary dissection. Due to the risk of entering
a false lumen, surgical management was planned. In
our patient, an internal mammary artery (IMA) graft
was not used because there were advanced fibrotic
changes and calcification in the aorta and its major
branches. A saphenous graft was preferred, as previous
reports have shown lesser venous involvement with this
procedure.5 A careful preoperative echocardiographic
examination with suprasternal views is suggested, which can provide the surgeon with adequate
information regarding graft choice. When intimal
thickening is intense and subclavian ostial stenosis
is detected, saphenous graft selection should be
given priority. No guidelines are currently available
regarding percutaneous intervention to protect the
LMCA following surgery for its dissection in patients
with Takayasuʹs arteritis. In conclusion, although Takayasu's arteritis is a rare disease, physicians should be mindful of serious complications such as coronary involvement and dissection. Transthoracic echocardiography with suprasternal views provides fast, reliable information and can be used as an alternative to CT and MRI. Future prospective echocardiographic studies examining the relationship between aorto-ostial involvement, aortic intimal thickness, and coronary involvement will be instrumental in providing information that can be used to detect patients at a high risk for coronary dissection.
Declaration of conflicting interests
Funding |
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| References | |||||||||
1) Takayasu M. A case with unusual changes of the central
vessels in the retina. Acta Soc Opthalmol Jpn 1908;12:554-5.
2) Arend WP, Michel BA, Bloch DA, Hunder GG, Calabrese
LH, Edworthy SM, et al. The American College of
Rheumatology 1990 criteria for the classification of
Takayasu arteritis. Arthritis Rheum 1990;33:1129-34.
3) Lupi-Herrera E, Sánchez-Torres G, Marcushamer J,
Mispireta J, Horwitz S, Vela JE. Takayasu's arteritis.
Clinical study of 107 cases. Am Heart J 1977;93:94-103.
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