Cazuri
Cazuri
Cazuri
doi:10.1093/ehjci/jew257
899 900
Asymptomatic very late presentation of ALCAPA Usefulness of 3-dimensional contrast echocardiography in the diagnosis of a
E. Cambronero Cortinas1; AE. Gonzalez Garcia2; M. Bret Zurita3; D. Garcia Hamilton2; left ventricular pseudoaneurysm after acute myocardial infarction
MJ. Corbi Pascual4; J. Ruiz Cantador2; JM. Oliver Ruiz5
901
Peri-procedural jailing of septal perforator branch retrospectively identified
using speckle tracking echocardiography
R. Sorrentino; F. Lo Iudice; T. Niglio; E. Stabile; M. Galderisi; B. Trimarco
Federico II University Hospital, Advanced biomedical science, Naples, Italy
Background: Jailing of septal perforator branches following percutaneous coronary
Abstract 899 Figure.
intervention (PCI) of left anterior descending artery (LAD) is a possible complication
that can lead to ECG ischemia-related changes, conduction disturbances, ventricular Conclusion: Anomalous left coronary artery from pulmonary artery (ALCAPA) is not
arrhythmias, peri-procedural myocardial infarction and even complete heart block. considered an inheritable congenital cardiac defect but is a rare congenital cardiac
The effect of septal branches jailing related occlusion on left ventricular (LV) function malformation. It presents predominantly in infancy or adulthood with features of myo-
and its relevant prognostic value is controversial. Speckle tracking echocardiography cardial ischemia, heart failure or sudden cardiac death. However, the prognosis is
(STE) derived longitudinal strain, a sensitive tool for diagnosis of myocardial ischemia, good with early surgical correction, but awareness of this condition is essential for
allows to highlight changes in ischemic area not otherwise detectable with visual eval- prompt diagnosis and referral to a tertiary cardiac center.
uation. Case Report: A 63–years old male with history of hypertension and smoke
habit referring for acute chest pain was admitted to cath lab with diagnosis of anterior
STEMI. Patient was hemodynamically stable, still symptomatic for angina, had no
signs of cardiac failure. Ultrasensitive troponine I was 191 pg/ml (cut-off point ¼0-34).
Coronary angiography revealed a critical long thrombotic stenosis of proximal LAD,
treated by balloon angioplasty and implantation of one drug eluting stent (3 x 34 mm)
obtaining TIMI 3 final flow. Circumflex coronary artery had a non-culprit critical steno-
sis (70%) with indication for staged PCI. Patient was transferred to coronary care unit
and underwent echo-Doppler including STE. Bull’s eye evaluation of LV longitudinal
strain identified a dysfunctional area involving mainly anterior septum and, with lesser
degree, posterior septum and anterior wall ;global longitudinal strain (GLS) was -
903
Coronary artery compression by aneurysmal pulmonary artery
RG. Badea; R. Enache; M. Serban; D. Gherasim; P. Platon; C. Ginghina
Institute of Cardiovascular Diseases Prof. C.C. Iliescu, Cardiology, Bucharest,
Romania
Introduction. Coexistent congenital heart defects, CHD raise difficulties in manage-
ment of both pediatric and adult patients. Therapeutic mishandling in childhood is not
rare and it echoes in present times by implying a high risk surgical profile and by limit-
ing the benefit of medical and percutaneous intervention.
Case report. 43 year old male presents for evaluation having a medical history of
complex CHD: small subpulmonary ventricular septal defect (VSD), closure of persis-
tent ductus arteriosus, PDA and angioplasty for aortic coarctation, preoperatory pul-
monary to systemic pressure ratio of 0.75 and late postoperatory reevaluation showed
Abstract 901 Figure. a ratio of 0.49. Problem and procedures. 6 minute walk test: 399m, desaturation from
91% to 82%, 10 mmHg fall in BP. Echocardiography revealed small subpulmonary
902 VSD and aneurysmal pulmonary artery, PA (main PA 57mm); biventricular hypertro-
phy, right ventricle, RV with mild systolic dysfunction, estimated systolic PA pressure,
Anomalous origin of the left coronary artery from the pulmonary artery
sPAP of 96mmHg; moderate to severe pulmonary regurgitation, moderate subvalvular
(ALCAPA)
aortic stenosis, mild to moderate aortic regurgitation. Catheterisation showed severe
Y. Hassan1; E. Elsharkawy2; R. Laymouna1; M. Elgowelly2; A. Almaghraby2 pulmonary arterial hypertension, PH (mean PAP 91 mmHg), pulmonary arterial resist-
1
International Cardiac Center Hospital, cardiology, Alexandria, Egypt; 2Alexandria ance 12,1 Wood units, Qp:Qs 1,41. Coronarography revealed ostial stenosis of 50-
University, cardiology, Alexandria, Egypt 60% of the left main coronary artery, LMCA which had a 7 mm diameter.
Introduction: Anomalous origin of the left coronary artery from the pulmonary artery Cardiopulmonary testing defined Weber class B.
(ALCAPA) is a rare but serious congenital cardiac anomaly. Its occurrence is gener- Questions and problems. The double aortic valvulopathy generates low diastolic
ally similar between males and females. coronary perfusion insufficient for the biventricular hypertrophy. Moreover, LMCA suf-
fers from extrinsic compression. This scenario raises 3 problems: 1) repair of aortic
Case report: A 19-year-old male patient, with no history of diabetes mellitus nor?hy-
valvulopathy; 2) closure of VSD; 3) dilation of LMCA stenosis.
pertension. He did not experience any previous attacks of chest pain, dyspnea or syn-
Answers and discussions. 1) Correction of the aortic disease is to be reevaluated
cope. He presented to our facility after resuscitation from sudden cardiac?arrest?while
given its moderate grade and natural slow progression. 2) VSD is too small to close
playing football. Upon examination, the patient had stable vital signs and an?unre-
and also acts as pressure release valve, its correction would cause right ventricular
markable clinical examination. Electrocardiogram showed normal sinus rhythm with
no ST segment abnormalities. Routine lab investigations were unremarkable?except decompensation. 3) However we support either pulmonary arterioplasty if the dilation
for weak positive troponin test. A Chest X-ray showed an average cardiac shadow. is progressive, or stenting of LMCA, high risk lesion: ostial position, supplemental
Echocardiography revealed normal data including normal left ventricular dimensions sPAP rise with physical exercise, more cardiovascular risk factors in time. The wide
and function. Multi-detector computed tomography revealed that the left main coro- LMCA constitutes an anatomical advantage and for now he is on sildenafil with satis-
factory results.
nary artery arising from the main pulmonary trunk then bifurcating to give left anterior
Conclusions and implications. PH in adults with CHD is not rare, mainly because
descending artery (LAD) and left circumflex artery (LCX). The right coronary artery
overdue surgical interventions in childhood. We expect a decline in this phenomenon
was arising normally from the Aorta (from right sinus of Valsalva).
after years of implementing PH guidelines. This should be endorsed by detailed CHD
The patient was referred for surgery. The left main coronary artery was resected from
management standardisation. Another point is validation of previously described fac-
the pulmonary artery and implanted to the aortic root.
Follow up multi-detector computed tomography (one year later) showed that the left tors for extrinsic LMCA compression: PA>40 mm, PA:aorta ratio>1,21, presence of
main coronary artery arising from the aortic root with good distal flow. All coronary PH. Given the low pretest probability of atherosclerosis PH patients rarely undergo
arteries were healthy with good flow. coronarography, but we promote that even without manifest ischemia, those with
compression risk factors should be investigated accordingly.
905
Single coronary ostium from the right aortic sinus of valsalva
Abstract 903 Figure.
R. Laymouna1; E. Elsharkawy2; Y. Hassan1; M. Elgowelly2; A. Almaghraby2
1
International Cardiac Center Hospital, cardiology, Alexandria, Egypt; 2Alexandria
904 University, cardiology, Alexandria, Egypt
A rare complication of myocardial infarction: pseudoaneurysm leading to Introduction: Single coronary ostium anomalies are rare conditions found in less
ischaemic VSD than 0.03% of the general population. One of these rare anomalies is the left main
TD. Heseltine; E. Lima; JM. Cino-Polla coronary artery arising from the right coronary artery. Although these anomalies are
Whiston Hospital, Cardiology, Liverpool, United Kingdom present at birth they are not diagnosed until older age.
Case report: A 63-year-old female patient, non-smoker, with medical history of diabe-
Introduction: Pseudoaneurysm is an increasingly rare complication of acute myocar-
tes mellitus and hypertension. She started complaining of exertional chest pain in the
dial infarction (AMI). This is recognised as an acute surgical emergency. The modern
past six months, which was relieved spontaneously. She presented to our facility com-
era of early invasive strategy combined with new potent antiplatelet agents have
plaining acute retrosternal chest pain. Upon examination, the patient had stable vital
greatly reduced the incidence of this often lethal complication. Urgent echocardiogra-
signs and an unremarkable clinical examination. Electrocardiogram was unremark-
phy is an essential tool in the assessment of patients presenting with pseudoaneur-
able. Routine laboratory investigations were unremarkable (including negative tropo-
ysm. We describe a case of pseudoaneurysm associated with ischaemic ventricular
nin test). Echocardiography revealed normal left ventricular dimensions and function.
septal defect (VSD) following delayed presentation of inferior AMI.
128-multidetector Computed tomography coronary angiography showed a single ori-
Case Report: A 67 year old patient was admitted with increasing exertional shortness
gin coronary artery arising from the right aortic sinus of Valsalva. An anomalous left
of breath over a two week period. He had a medical background of gallstones. His
main coronary artery (LM) was noticed to arise from the right coronary artery (RCA)
cardiac risk factors included smoking and a positive family history of ischaemic heart
passing anterior to the pulmonary outflow trunk to reach the anterior inter-ventricular
disease.
groove to give the left anterior descending artery (LAD) and the left circumflex artery
His initial ECG showed inferior Q waves with borderline ST elevation in the inferior
(LCX). The left anterior descending artery (LAD) was a short vessel. The right coro-
leads (figure 1). His chest radiograph showed evidence of pulmonary oedema. The
nary artery was a very large vessel. All these coronary arteries were healthy with
troponin was borderline elevated. He was treated initially with dual antiplatelets, low
good flow.
molecular weight heparin and intravenous diuretics. Clinical examination revealed
The patient was assured that she had no coronary artery disease but all she had was
bilateral crepitations with a loud pansystolic murmur at the left sternal edge. He was
a rare variation of coronary artery origin with no specific disease.
haemodynamically stable throughout.
Conclusion: Single coronary origin is a rare type of coronary artery anomalies.
Urgent echocardiography revealed a large pseudoaneurysm involving the mid-inferior
Multidetector computed tomography is one of the best non-invasive modalities in diag-
posterior wall. The cavity of the pseudoaneurysm communicated with the right ven-
nosis of coronary artery anomalies.
tricle (figures 2 and 3). The right ventricle was non-dilated with good systolic function.
The pulmonary artery systolic pressure was elevated at 50mmHg. The left ventricular
function was hyperdynamic.
This finding was later confirmed on cardiac CT with VSD measurements calculated at
1.3cm x 2.1cm. The patient was subsequently transferred to our local tertiary centre
where he underwent angiography and intra-aortic balloon pump placement. Once sta-
bilized he underwent VSD closure with resection of the left ventricular pseudoaneur-
ysm with saphenous vein grafting to the mid-LAD. The patient was discharged and he
remained asymptomatic at three months follow up.
Questions, Problems and Differential Diagnosis
1) Which are the differential diagnoses in patients with a murmur in the setting of
AMI?
2) What are the echocardiographic clues to differentiate true aneurysm with false or
pseudoaneurysms? 4) 3) What are the treatment options for patients with pseudoa-
neurysms and true aneurysms post MI?
4) What is the mortality of patients with pseudoaneurysms?
Answers and Discussion: 1) Ischaemic mitral regurgitation (MR) which may be sec-
ondary to a large area of infarct or papillary muscle rupture. Acute VSD. Tricuspid
regurgitation in the setting of right ventricular infarct. The presence of a murmur in a
patient with AMI especially if clinically unstable should trigger an urgent Echo.
2) True Aneurysm: Wide neck, usually at apex (only 3% inferior). Pseudoaneurysm:
narrow neck (less than 50% aneurysm diameter), thrombus support, pericardial
effusion.
3) Surgical intervention is the treatment of choice in patients with pseudoaneurysm. In
true aneurysms the risk of surgery against medical treatment can be considered Abstract 905 Figure.
depending on symptoms, location of aneurysm, LV function, presence of arrhythmia.
4) 50% mortality with medical treatment and 10% with surgery.
907
One serious complication after myocardial infarction, isn’t that enough?
K. Sawicka; M. Prasal; M. Tomaszewski; A. Wojtkowska; A. Tomaszewski
Medical University of Lublin, Cardiology Department, Lublin, Poland
A 47-year- old man was admitted to the Neurology Department due to ischemic stroke
(involving thalamus and pons, due to embolism of basic artery). There was no pre-
vious medical history. After ECG cardiological consultation was performed. The ECG
demonstrated signs consistent with an extensive anterior myocardial infarction (QS Abstract 907 Figure.
V1-V6 and persistent ST –elevation). Cardiac markers, including troponin I, creatine-