Chylothorax is an unusual cause of pleural effusion after the neonatal period in children without a previous history of cardiothoracic surgery. Determination of the causes of this condition can be often challenging. Herein, we present a case of a 6-month-old male infant, presenting with sudden severe breathlessness, which was later diagnosed as spontaneous left-sided chylothorax.

We describe a case with pacemaker implantation for cardiac resynchronization therapy (CRT) in a patient with complex congenital heart disease, facilitated by cardiac computed tomography (CT) and coronary sinus (CS) venography. A 37-year-old male presented with congenitally corrected transposition of the great arteries and mesocardia, along with a history of two open heart surgeries (closure of ...

Silver Russell Syndrome (SRS) is a rare condition (1/3000 - 1/100,000 newborns). We present a female infant with SRS, cardiac malposition and asymmetric enlargement of the clitoris. She is the first child of Greek nonconsanguinous parents, born at 38 weeks gestation, following in vitro fertilisation (IVF). The patient had intrauterine growth retardation, body asymmetry, enlarged clitoris, hemih...

Single ventricle is that condition in which both atrioventricular (A-V) orifices enter a common ventricular sinus, from which the arterial trunks emerge with their coni. The following types of single ventricle were found: (1) with regular (noninverted) transposition in levocardia; (2) with inverted transposition in levocardia; (3) with normal position of arterial trunks in levocardia; (4) in de...

OBJECTIVE To describe the anatomy, associated anomalies and outcome of 30 cases of congenitally corrected transposition of the great arteries (ccTGA) detected prenatally. METHODS This was a retrospective observational study of the 30 cases of ccTGA confirmed at autopsy or postnatal echocardiography seen at one of three referral centers from 1994 to 2003. The following data were considered: ge...

BACKGROUND Congenitally corrected TGA (CC-TGA) is characterized by discordant atrioventricular and ventriculo arterial connections. In absence of right ventricular outflow tract obstruction (RVOTO), repair by atrial and arterial switches remains a challenging procedure for which long term follow-up is uncertain. METHODS From 1995 to 2007, 20 patients (median age: 26 months) with CC-TGA had do...

To cite: Haththotuwa HR, Dubrey SW. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013201046 DESCRIPTION At first glance these chest radiographs appear similar. Closer inspection suggests ‘dextrocardia’ (figure 1A) and ‘dextroposition’ (figure 1B). Confusing terminology is helped if the heart’s position within the thorax and point of direction of the apex is des...

Presentation A 19-year-old male with congenitally corrected transposition of the great arteries (ccTGA; S, L, L–situs solitus, l-loop, l-transposition) presented with recurrent frequent palpitations, fatigue, and effort intolerance. Previous history was significant for initial presentation with supraventricular tachycardia (SVT) at the age of 14 years. Transthoracic echocardiography at that tim...

HomeCirculation: Arrhythmia and ElectrophysiologyVol. 14, No. 4Template Beat Free AccessLetterPDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessLetterPDF/EPUBTemplate BeatA Novel Marker for Left Bundle Branch Capture During Physiological Pacing Shunmuga Sundaram Ponnusamy...