A rare case of two superior vena cava with two azygos veins in a cadaver

Q4 Medicine
Archana Singh, Rakesh Gupta, Priya Adhaya, Aleeza Muneer
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引用次数: 0

Abstract

In embryonic life developmental malformation of thoracic veins can lead to anomalies of the Superior vena cava and major thoracic veins like Azygos system. Double superior vena cava and double azygos vein are rare congenital anomaly with the incidence of 0.3%. These types of congenital anomalies may or may not be presented with clinical symptoms. This case was noted during the routine cadaveric dissection of thoracic region and heart for medical students in department of Anatomy, we found double superior vena cava (persistent left superior vena cava) along with double (paired) azygos vein in a female cadaver. Right superior vena was formed by the union of right subclavian and right internal jugular vein which receives the arch of right azygos before it opened into the right atrium. Left superior vena cava was formed by the union of left subclavian and left internal jugular vein and it also receives the arch of left azygos vein before it entered into the right atrium. In present case coronary sinus was separated from left persistent superior vena cava and it opened in the persistent left superior vena cava. There was no communication between both the superior vena cava. On right side Azygos vein was normal and open into right superior vena cava. On the left side hemiazygos was in continuation with the accessory azygos vein and it also forming the arch and opened into persistent left superior vena cava. There were no other congenital anomalies present in the heart. These types of congenital anomalies extremely very rare where the left superior vena cava opens into the right atrium directly and coronary sinus opens in to this left superior vena cava. Majority of such types of cases remain asymptomatic. Some cases may be detected accidently during diagnostic or surgical procedures like cardiac angiography, cardiac catheterization, by- pass and dialysis or during autopsy or institutional cadaveric dissection.
尸体中罕见的双上腔静脉伴奇静脉病例
胚胎期胸静脉发育畸形可导致上腔静脉和胸大静脉(如奇静脉系统)异常。双上腔静脉和双奇静脉是一种罕见的先天性畸形,发生率为0.3%。这些类型的先天性异常可能有临床症状,也可能没有临床症状。在为解剖学系的医学生进行的胸部和心脏的常规尸体解剖中注意到了这个病例,我们在一具女性尸体中发现了双上腔静脉(持续性左上腔静脉)和双(成对)奇静脉。右上静脉由右锁骨下静脉和右颈内静脉合并形成,右颈内静脉在进入右心房之前接受右奇静脉弓。左上腔静脉由左锁骨下静脉和左颈内静脉合并而成,在进入右心房之前还接受左奇静脉弓。在本例中,冠状窦与左持续性上腔静脉分离,并在持续性左上腔静脉中开放。两个上腔静脉之间没有连通。右侧的奇静脉是正常的,通向右上腔静脉。在左侧,半奇静脉与副奇静脉相连,并形成拱形,通向持久的左上腔静脉。心脏没有其他先天性异常。这些类型的先天性异常极为罕见,左上腔静脉直接通向右心房,冠状窦通向左上腔。大多数此类病例仍然没有症状。有些病例可能是在诊断或手术过程中偶然发现的,如心脏血管造影术、心导管插入术、旁路和透析,或尸检或机构尸体解剖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
2
审稿时长
16 weeks
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