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Morphometry of the aortic arch and its branches

. (1991). Anatomie topographique, descriptive et topographique 2: Le cou. Le thorax . (pp. 798-807, 1042-1048). Paris: Ed. Simep 10. Gorun M. & Mihalache C. (2010). The Branches of the Aortic Arch. Three case Presentation of anatomical variants. Ars Med. Tomitana. Vol. XVI, Nr.2 (61), 94-96 11. Young S., Yong-Gu C., Won-Han S., Soo- Bin I., Sun-Chul H. & Bum-Tae K. (2008). A Morphometric Study on Cadaveric Aortic Arch and Its Major Branches In 25 Korean Adults: The Perspective of Endovascular Surgery. J. Korean. Neurosurg. Soc . 44

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Morphological characteristics of the aortic arch organization

References 1. Guillem Ph., Triboulet J.P., Fontaine Ch. & Bailleul J.P. (1999). Les arcs aortique droits: classification anatomique et embryologique. Morphologie. 83 (262), 13-38 2. Grande N.R., Costa A., Silva E., Sousa Pereira A. & Aguas A.P. (1995). Variations in the Anatomical Organization of the Human Aortic Arch. A Study in a Portuguese Population. Bull. Assoc.Anat . 244, 19-22. 3. Il-Young Shin, Yong-Gu Chung, Won-Han Shin, Soo-Bin Im, Sun-Chul Hwang & Bum-Tae Kim. (2008). A Morphometric Study

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Aortic arch branches’ variations detected on chest CT

References 1. Nayak SR, Pai MM, Prabhu LV, D’Costa S, Shetty P. Anatomical organization of aortic arch variations in the India: embryological basis and review. J Vasc Bras. 2006; 5:95-100. 2. Nelson ML, Sparks CD. Unusual aortic arch variation: distal origin of common carotid arteries. Clinical anatomy (New York, NY. 2001; 14:62-5. 3. Natsis KI, Tsitouridis IA, Didagelos MV, Fillipidis AA, Vlasis KG, Tsikaras PD. Anatomical variations in the branches of the human aortic arch in 633 angiographies: clinical

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Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report

specială. Cluj: Casa Cărții de Știință, 2006,(pp. 214-217). 6. Roland W. Dudek. Development of the arterial system. Embryology in Gigh-Wield Heart. Lippincott Williams & Wilkins, 2006 (pp. 11-13). 7. Lone GN, Rathore SS, Malik JA, Ashraf HZ, Qadri AA. Double aortic arch masquerading as bronchial asthma for five decades. Asian Cardiovasc Thorac Ann., 2012; 20(3):338-40. 8. Satyapal KS, Lazarus L, Shama D. Double aortic arch: an unusual congenital variation. Surg Radiol Anat., 2013; 35(2):125-9. 9. Fraser CD Jr, Carberry KE. Congenital heart disease

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Endo and exo aortic morphometry (endoluminal) in the aortic arch and its branches

. 9. Kamina, P. (2002). Précis d’anatomie clinique. Tome II. Paris: Maloine. 10. Bouchet, A. & Cuilleret J. (1991). Anatomie topographique, descriptive et topographique. 2. Le cou. Le thorax. Paris: Simep. 11. Young, S., Yong-Gu, C., Won-Han, S., Soo- Bin, I., Sun-Chul, H. & Bum-Tae, K. (2008). A Morphometric Study on Cadaveric Aortic Arch and Its Major Branches In 25 Korean Adults: The Perspective of Endovascular Surgery. J.Korean. Neurosurg.Soc., 44, 78-83. 12. Gorun, M. & Mihalache, C. (2010) The Branches of the

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An unusual origin of the right subclavian artery – arteria lusoria

, 2013. 5. Derbel B. et al.: Aberrant right subclavian artery or arteria lusoria: a rare cause of dyspnea in children. Ann. Vasc. Surg., 26, 1-4, 2012. 6. Dziekiewicz M. et al.: Variations in the anatomy of the branches of an aortic arch-two cases. Acta Angiol., 12, 80-84, 2006. 7. Ergun E. et al.: Anatomicalvariations in branching pattern of arcus aorta: 64-slice CTA appearance. Surg. Radiol. Anat., 35, 503-509, 2013. 8. Głowacki J. et al.: Technika obrazowania. Współistnienie koarktacji aorty z

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Markers of Atherosclerosis in Hypertensive Patients with Less Advanced Chronic Kidney Disease

. Verdoia M, Barbieri L, Di Giovine G et al. Neutrophil to Lymphocyte Ratio and the Extent of Coronary Artery Disease: Results From a Large Cohort Study. Angiology. 2016;67(1):75-82. 17. Zhou S, Cai B, Zhang Y, Wang L, Liu X, Xu G. The Relationship between Neutrophil-to-Lymphocyte Ratio and Aortic Arch Calcification in Ischemic Stroke Patients. J Stroke Cerebrovasc Dis. 2017;26(6):1228-32. 18. Yoshitomi R, Nakayama M, Sakoh T et al. High neutrophil/lymphocyte ratio is associated with poor renal outcomes in Japanese patients with chronic kidney disease. Ren

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Aberrant right subclavian artery - a marker for chromosomal abnormalities?

-221. 4. Goldstein, W.B. (1965). Aberrant right subclavian artery in Mongolism. Am J Roentgoenol Radium Ther Nucl Med. 95, 131-134. 5. Yoo, S.J., Bradley, T. & Lee, Y.H., et al. (2003). Sonographic diagnosis of aortic arch anomalies. Ultrasound Obstet Gynecol. 22, 535-546. 6. Chaoui, R., Thiel, G. & Heling, K.S. (2006). Prevalence of an aberrant right subclavian artery in fetuses with chromosomal aberrations. Ultrasound Obstet Gynecol. 28, 414. 7. Nicolaides, K.H., Spencer, K., Avigidou, K., Faiola, S. & Falcon, O

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Anatomical Considerations of the Ostium of the Subclavian Artery

thorax. Paris: Simep; 1991 6. Kamina P. Anatomie clinique. Tome 3. Thorax. Abdomen. Paris: Maloine; 2007 7. Testut L. Traité d’anatomie humaine. Angéiologie, livre IV, Paris: Gaston Doin; 1921 8. Shin IY, Chung YG, Shin WH, Im SB, Hwang SC, Kim BT. A morphometric study on cadaveric aortic arch and its major branches in 25 Korean adults: the perspective of endovascular surgery. Journal of Korean Neurosurgical Society. 2008 Aug;44(2):78. 9. Malik S. The morphology of the abdominal aorta. Doctoral thesis, Constanţa: University “Ovidius” of

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Transthoracic 3D Echocardiographic Imaging of Type A Aortic Dissection – Case Presentation


In type A aortic dissection (AoD) an early and accurate diagnosis is essential to improve survival, by applying urgent surgical repair. 3D transthoracic echocardiography (3D-TTE), an advanced noninvasive imaging technique, could offer a comprehensive evaluation of the ascending aorta and aortic arch in this regard. Both modalities of real-time 3D imaging – live 3D and full-volume aquisition – proved to be useful in evaluating the localization and extent of AoD. Our case illustrates the utility of 3D-TTE in the complex assessment AoD. By providing the proper anatomical dataset, 3D-TTE could facilitate considerably the diagnosis of type A AoD.

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