1.Surgical Treatment of Isolated Phlebectasia of the Forearm: A case report.
Woo Surng LEE ; Yo Han KIM ; Hyun Keun CHEE ; Jae Joon HWANG ; Song Am LEE ; Ho Sung JUNG
The Korean Journal of Thoracic and Cardiovascular Surgery 2010;43(6):764-768
Phlebectasia of the venous system of the upper limb is very rare and it does not have a well-defined etiology. Phlebectasia means isolated fusiform or saccular dilatation of the venous system and isolated phlebectasia of the forearm may present as a painless cosmetic deformity or it may cause pain, decreased range of movement, compression on adjacent structures, bleeding, thrombosis and consumptive coagulopathy. We report here on a case of isolated phlebectasia of the forearm and we briefly review the relevant literature.
Congenital Abnormalities
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Cosmetics
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Dilatation
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Forearm
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Hemorrhage
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Thrombosis
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Upper Extremity
;
Veins
2.Subaortic Left Brachiocephalic Vein.
Chan Kwon PARK ; Ki Jun KIM ; Min Kyong PARK ; Hong Jun YANG ; Jin Man CHO ; Doo Soo JEON ; Man Young LEE
Korean Circulation Journal 2006;36(8):605-607
Subaortic left brachiocephalic vein is a rare congenital anomaly that is sometimes found in the normal population. We report here on a case of subaortic left brachiocephalic vein that was detected incidentally by performing contrast transesophageal echocardiography (TEE) with using agitated saline and computed tomography (CT).
Brachiocephalic Veins*
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Dihydroergotamine
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Echocardiography, Transesophageal
4.Echocardiographic diagnosis of total anomalous pulmonary venous connection.
Mingxing, XIE ; Xiaofang, LU ; Xinfang, WANG ; Qing, LU ; Yali, YANG
Journal of Huazhong University of Science and Technology (Medical Sciences) 2004;24(2):192-5
To investigate the value of echocardiography in the diagnosis of total anomalous pulmonary venous connection (TAPVC), 16 patients in our hospital were diagnosed to have TAPVC by echocardiography from year 1994 to 2001. In 11 cases the results of echocardiography were compared to those of surgery. Each patient was examined by using a combination of precordial, suprasternal and subcostal windows to visualize all the pulmonary veins and their drainage sites, common pulmonary venous trunk, and other associated abnormalities. Of the 16 cases, the drainage sites were as follow: supracardiac in 10, via vertical vein in 9, directly to superior vena cava in 1; cardiac in 5, via coronary sinus in 2, directly to right atrium in 3. Diagnoses were correctly made in all the 11 cases as confirmed by surgery. Echocardiography can also assess pulmonary arterial pressure and detect other associated abnormalities. It is concluded that echocardiography is the preferred examination method in the diagnosis of TAPVC before surgery. With careful examination using multiple windows and sections, TAPVC can be accurately diagnosed by echocardiography.
*Echocardiography, Doppler, Color
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Heart Defects, Congenital/*ultrasonography
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Pulmonary Veins/*abnormalities
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Pulmonary Veins/ultrasonography
5.Pulmonary arteriovenous fistula in one child.
Jun-Xue NI ; Yan MA ; Jian WAN ; Peng LI
Chinese Journal of Contemporary Pediatrics 2008;10(3):419-421
8.Double external jugular vein and other rare venous variations of the head and neck.
Varsha SHENOY ; Perumal SARASWATHI ; Gunapriya RAGHUNATH ; Jayakumar Sai KARTHIK
Singapore medical journal 2012;53(12):e251-3
Superficial veins of the head and neck are utilised for central venous cannulation, oral reconstruction and parenteral nutrition in debilitated patients. Clinical and sonological examinations of these veins may provide clues toward underlying cardiac pathology. Hence, although variations in these vessels are common, a sound knowledge of such variations becomes clinically important to surgeons, radiologists and interventional anaesthetists. We report a rare case of a left-sided double external jugular vein where the common facial vein continued as the second external jugular vein, and where there was a communicating channel between the internal jugular vein on the same side and the anterior jugular vein.
Brachiocephalic Veins
;
abnormalities
;
Cadaver
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Head
;
blood supply
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Humans
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Jugular Veins
;
abnormalities
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Male
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Middle Aged
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Neck
;
blood supply
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Subclavian Vein
;
abnormalities
;
Vascular Malformations
;
diagnosis
9.Left costocervical vein malformation with anomalous ramification of aortic arch in a dog.
Young Sam NAM ; Choong Hyun LEE ; Dae Won CHUNG ; Yeo Sung YOON ; Heungshik S LEE ; In Se LEE
Journal of Veterinary Science 2003;4(3):205-208
This report describes coexistence of anomalous branches of the aortic arch and the costocervical vein malformation in a German shepherd dog. The first branch of the aortic arch was a bicarotid trunk that divided into the left and right common carotid arteries. The next branch to leave the aortic arch was a common trunk for the right and left subclavian arteries, a bisubclavian trunk, which was immediately bifurcated. The right subclavian artery passed over the esophagus forming a deep groove, so-called incomplete vascular ring on the dorsal wall of the esophagus. Although the esophagus was constricted by the right subclavian artery dorsally and by the trachea ventrally, no clinical symptoms of esophageal obstruction and dysphagia were observed. The left costocervical vein coursed caudoventrally, passed over the aortic arch, and entered the left ventricle. This vessel was much smaller than the right costocervical vein and was partially occluded at its origin.
Animals
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Aorta, Thoracic/*abnormalities
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Carotid Artery, Common/abnormalities
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Dog Diseases/congenital/*pathology
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Dogs
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Fatal Outcome
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Female
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Subclavian Artery/abnormalities
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Veins/*abnormalities
10.Cavernous Transformation of Portal Vein with Right Lobe Hypoplasia of Liver: A Case Report.
Chul Woon CHUNG ; Chang Moo KANG ; Jin Sub CHOI ; Byong Ro KIM
Korean Journal of Hepato-Biliary-Pancreatic Surgery 1999;3(2):163-167
Cavernous transformation of the portal vein that is resulted as a collateral vessel formation from a portal hypoplasia is very rarely to be observed in human being. Such an abnormal transformation can be caused by congenital defect of vein formation in the early embryonal development or congenital hematologic hypercoagulability which gives rise to the cavernous development of cavernous collateral branches. Acute thrombosis of portal vein can also be the cause of acquired cavernous transformation. In most cases it extends into the parenchyme of liver, and often has porto-systemic shunt (with left gastropiploic vein and varices around spleen) or porto-portal shunt (with varices around gallbladder). A 48 years old male patient underwent splenectomy at the age of 24 owing to splenomegaly. He had liver cirrhosis without hepatitis and alcohol history. Intrahepatic stone in left lateral lobe of liver was diagnosed in the course of medical treatment. The cavernous transformation of portal vein with right lobe hypoplasia was confrimed during the operation.
Congenital Abnormalities
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Hepatitis
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Humans
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Liver Cirrhosis
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Liver*
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Male
;
Middle Aged
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Portal Vein*
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Splenectomy
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Splenomegaly
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Thrombophilia
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Thrombosis
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Varicose Veins
;
Veins