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Published on: April 11, 2025
Case Report: An Anomalous Left Hepatic Venous Connection in a Patient With Unexpected Cyanosis
1Department of Cardiothoracic Surgery, Xiangya Hospital, Central South University, Changsha, China.
Insights
An anomalous left hepatic venous connection can complicate cardiac surgery. Accurate preoperative diagnosis is crucial to prevent reoperation and ensure timely treatment for patients with congenital heart disease.
Area of Science:
- Cardiology
- Pediatric Cardiac Surgery
- Congenital Heart Disease
Background:
- Anomalous left hepatic venous (LHV) connections are rare cardiac malformations.
- Physiologically benign in isolation, they require surgical consideration when associated with other cardiac lesions, particularly in total cavopulmonary connection (TCPC) procedures.
Observation:
- A 7-year-old boy with a history of bilateral superior vena cava pulmonary anastomosis presented with severe cyanosis post-extracardiac total cavopulmonary connection (ETCPC).
- The patient experienced a significant drop in oxygen saturation to 60-70% after the ETCPC operation.
Findings:
- Postoperative echocardiography and CT revealed an anomalous LHV entering the right atrium.
- The patient successfully underwent a staged TCPC with an intra-atrial tunnel technique for correction.
Implications:
- This case underscores the critical importance of precise preoperative diagnosis of anomalous LHV connections in pediatric cardiac surgery.
- Improved diagnostic accuracy can prevent unplanned reoperations and ensure optimal treatment timing, especially in resource-limited settings.
Abstract:
An anomalous left hepatic venous (LHV) connection is an extremely rare cardiac malformation, and left hepatic venous route abnormalities not associated with other cardiac lesions do not require surgical treatment because they are physiologically benign. However, when venous route abnormalities exist with associated cardiac lesions, the conduct of the cardiac surgical repair must accommodate the abnormal venous anatomy, especially in total cavopulmonary connection patients. Herein, we present a rare case of a 7-year-old Chinese boy about 1 year post bilateral superior vena cava pulmonary anastomosis who presented with severe cyanosis and was referred to our department. However, the patient showed an unexpected gradual decrease in blood oxygen saturation to 60-70% after the extracardiac total cavopulmonary connection (ETCPC) operation. Emergency echocardiography and computed tomography confirmed that the LHV entered the right atrium. Subsequently, the patient undergone completion of a staged TCPC with intra-atrial tunnel technique. This illustrative report highlights the essence of improving the preoperative accurate diagnosis to avoid unplanned reoperation in China, especially for the remote rural areas of eastern countries where the level of health care and services is relatively backward. Failure to identify anomalous LHV connection, in this case, will delay effective treatment past the optimal treatment time.
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