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Page 34
Volume 5
Journal of Current Research: Cardiology
Heart Congress 2018
November 21-22, 2018
2
nd
Global Heart Congress
November 21-22, 2018 Osaka, Japan
A heart or a boot?
Giuliana Cimino and Giuseppe Lavatura
Polyclinic University Paolo Giaccone, Italy
A
20-year-old refugee arrived at our emergency department for the presence of recurrent episodes of breathlessness, palpitation
and easy fatigue since childhood. In his country of origin he had never undergone investigations. His family history was devoid
of important and did not take any medication. The triad composed of exercise dyspnea, easy fatigue and palpitation suggested a
cardiac cause, and the presence of symptoms since childhood indicated that it was a systemic disease, although it could also be a
rheumatic endocarditis. It showed signs of chronic malnutrition (growth retardation) and acute (body mass hypotrophy). It was
plethoric, cyanotic and with severe digital hippocratism, signs that could be secondary to a congenital cyanogenic heart disease such
as the tetralogy of Fallot or Eisenmenger's syndrome. The cardiovascular objective examination revealed a pansystolic murmur at
the left inferior sternal angle, associated a thrill: findings present in both tricuspid deficiency and interventricular septal defects.
However, the absence of cannon-shot waves made tricuspid insufficiency unlikely. The second cardiac tone was intense, suggesting
the presence of pulmonary hypertension. On the other hand it was single and this indicated a pulmonary stenosis. The chest radiograph
revealed oligemic lung fields and a heart shaped like a boot. At the EKG (Electro Cardio Graphy) pulmonary P-waves, right axial
deviation and right bundle branch block were evident. The echocardiogram, which revealed a taking 2 cm defect of the membranous
portion of the interventricular septum with a right-left shunt; knight aorta with normal aortic diameter; right ventricular hypertrophy,
right atrial dilatation and infundibular stenosis, small left ventricle; 56% ejection fraction. At this point, the combination of cyanosis,
interventricular defect and pulmonary stenosis was characteristic of the tetralogy of Fallot. In cases like this, the surgical correction
must be performed as soon as possible. The boy was indeed transferred to cardiac surgery, where he continued the therapeutic
process, which was successful.
cimino.giuli@gmail.comCurr Res Cardiol 2018, Volume 5
DOI: 10.4172/2368-0512-C1-003