A very rare abnormal course of the thoracic venous system: Long journey to the right ventricle

نویسندگان

  • Yao Chang Wang
  • An Ning Feng
  • Wei Hsian Yin
  • Mason Shing Young
چکیده

Case report The patient had a history of coronary artery disease postcoronary artery bypass graft and was hospitalized for syncope due to atrial fibrillation with slow ventricular response, and underwent ventricular pacemaker implantation (VVIR mode). Under fluoroscopic guidance, a right ventricular screw-in lead was inserted via the cephalic vein. The course of the pacemaker leads deviated from the normal brachiocephalic pathway and ran dorsally along the left lateral aspect of the thoracic vertebra and across the thoracic vertebra to the right side at T6 level, and then ran to the right atrium via the superior vena cava (SVC), as shown in Figure 1 (A,B). Anomalous communication with the coronary sinus was excluded by placing a lead into the coronary sinus, which was not communicating with the pacemaker lead. Owing to the long course, the standard ventricular leads could not access the right ventricle. So a ventricular lead (TENDRIL ST 1888TC/65cm; St Jude Medical) was fixed with screws at the mid septum. The whole course was confirmed by electrocardiographic-gated 64-slice computed tomographic (CT) angiography with a 3-dimensional reconstruction, which revealed very short left brachiocephalic veins draining downward into the accessory hemiazygos vein (AHAZV) that communicated to the azygos vein (AZV)

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Cardiac Myxoma, a Rare But Most Common Encountered Cardiac Tumor: A Single Center Experience

Introduction: Cardiac myxoma is a benign and rare tumor, which can present with a grim phenomenon if the presentation is late or the diagnosis and surgery are delayed. The purpose of this study was to share our institutional experience of cardiac myxoma. Material and Methods: This retrospective study was conducted to evaluate patients undergoing procedures at a single tertiary care centre for t...

متن کامل

Large saphenous venous graft aneurysm mimicking atypical mediastinal mass.

BACKGROUND Saphenous venous graft (SVG) aneurysm is a very rare but potentially fatal complication of the coronary artery bypass surgery. CASE REPORT We reported a case of 72-year-old man admitted to hospital because of atypical chest pain related to body motions in horizontal position, especially to the left side. Pain was followed by dispnea, palpitations, fatigue, cough, yellow sputum expe...

متن کامل

Intracardiac Thrombosis in Sickle Cell Disease

In patients with sickle cell disease, thrombotic microangiopathy is a rare complication. Also in sickle cell disease, intracardiac thrombus formation without structural heart diseases or atrial arrhythmias is a rare phenomenon. We herein describe a 22-year-old woman, who was a known case of sickle cell-βthalassemia, had a history of recent missed abortion, and was admitted with a vaso-occlusive...

متن کامل

Cor Triatriatum Sinistrum Presenting as Cyanotic Congenital Heart Disease A Rare Case Report

  Cor triatriatum is an acyanotic congenital heart disease. We present a rare case of cor triatriatum sinistrum in a 6-month-old female infant who was presented with cyanosis and failure to thrive. The 2D transthoracic echocardiography and the Doppler color flow imaging showed a proximal venous chamber communicating to the distal left atrium  through restrictive opening to the low-pressure, dis...

متن کامل

Holt-Oram Syndrome: A Rare Variant

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 1  شماره 

صفحات  -

تاریخ انتشار 2015