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Journal articles on the topic 'Scimitars'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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1

Opfermann, Andreas, David Sasseville, and Riko Süssenguth. "Hethitisch māri- ,Sichelschwert(?)‘ aus archäologischer, philologischer und etymologischer Sicht." Altorientalische Forschungen 49, no. 1 (June 1, 2022): 104–22. http://dx.doi.org/10.1515/aofo-2022-0007.

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Abstract This paper addresses the Hittite word giš māri-, which designates a kind of weapon and is often translated as ‘mari-spear’. A philological re-evaluation of the Hittite attestations rather calls for the meaning ‘scimitar (sickle-shaped sword),’ which has previously been suggested but was largely disregarded. At the same time, archaeological evidence for the presence of scimitars in the Hittite culture is adduced. Subsequently, the role of this type of weapon in the ancient Near East is reassessed. Finally, a new Indo-European etymology for the word māri- is offered, which brings additional support for the meaning ‘scimitar (sickle-shaped sword).’

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2

Niayesh, Ladan. "Of Pearls and Scimitars: The Shakespearean Bazaar of Oriental Props." Actes des congrès de la Société française Shakespeare, no. 27 (December 13, 2009): 83–98. http://dx.doi.org/10.4000/shakespeare.1507.

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3

Hanes, Jay Michael, and Eleanor Weisman. "Mages and Scimitars: Finding Meaning in a Pre-adolescent’s Drawing." Art Education 61, no. 1 (January 2008): 45–50. http://dx.doi.org/10.1080/00043125.2008.11518987.

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4

KOHN, ALAN J., MANAMI NISHI, and BRUNO PERNET. "SNAIL SPEARS AND SCIMITARS: A CHARACTER ANALYSIS OF CONUS RADULAR TEETH." Journal of Molluscan Studies 65, no. 4 (November 1999): 461–81. http://dx.doi.org/10.1093/mollus/65.4.461.

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5

Jerep, Fernando C., and Luiz R. Malabarba. "A new species of Serrapinnus Malabarba, 1998 (Characidae: Cheirodontinae) from Rio Grande do Norte State, northeastern Brazil." Neotropical Ichthyology 12, no. 2 (June 2014): 301–8. http://dx.doi.org/10.1590/1982-0224-20130218.

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Serrapinnus potiguar, new species, is described from the rio Ceará-Mirim, a coastal drainage in the Rio Grande do Norte State, northeastern Brazil. The new species is distinguished from the other species of the genus by the shape and arrangement of the ventral procurrent caudal-fin rays of the sexually dimorphic males; where the hypertrophied elements present the shape of a series of scimitars arranged radially, forming a semi-circle on the ventral margin of the caudal peduncle. Furthermore, the new species is diagnosed from S. heterodonand S. piaba, sympatric congeners from the northeastern Brazilian drainages, respectively by the presence of incomplete lateral line and teeth bearing at most five cusps.

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6

Hughes, David W. "Book Review: Comets in History: The Greatest Comets in History: Broom Stars and Celestial Scimitars." Journal for the History of Astronomy 41, no. 4 (November 2010): 518–19. http://dx.doi.org/10.1177/002182861004100414.

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7

Kalfa, David. "Commentary: Turkish blacksmiths were expert craftsmen at manufacturing scimitars; congenital cardiac surgeons need to be expert craftsmen at repairing them." JTCVS Techniques 4 (December 2020): 219–20. http://dx.doi.org/10.1016/j.xjtc.2020.08.059.

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8

Orchiston, Wayne. "<italic>The Greatest Comets in History. Broom Stars and Celestial Scimitars</italic>, by David Seargent." Journal of Astronomical History and Heritage 12, no. 1 (March 1, 2009): 87. http://dx.doi.org/10.3724/sp.j.1440-2807.2009.01.12.

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9

Corvol, Fany, Sébastien Hascoet, Emmanuel Le Bret, and Nadia Nathan. "Scimitar syndrome with vein stenosis in an infant." BMJ Case Reports 17, no. 5 (May 2024): e259955. http://dx.doi.org/10.1136/bcr-2024-259955.

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Scimitar syndrome is characterised by right lung hypoplasia and abnormal pulmonary venous return, known as the ‘scimitar vein’. We report the case of an infant girl with scimitar syndrome who developed a severe respiratory distress mimicking asthma. Pulmonary hypertension (PH) was diagnosed, attributed to scimitar vein stenosis and a left-to-right shunt. Scimitar vein stenosis, a rare complication of scimitar syndrome, can lead to severe PH, highlighting the importance of prompt management in specialised care centres.

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10

Nitta, Manabu, Yoshihiro Ishikawa, Daisuke Machida, Munetaka Masuda, Koichi Tamura, and Kazuo Kimura. "Minimally invasive thoracoscopic surgery for scimitar syndrome variant." Asian Cardiovascular and Thoracic Annals 28, no. 1 (July 19, 2019): 48–51. http://dx.doi.org/10.1177/0218492319865446.

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A 19-year-old symptomatic female was diagnosed with scimitar syndrome variant, in which the right pulmonary veins drained into the left atrium and inferior vena cava through an anomalous venous connection (the so-called scimitar vein). Because of the long distance between the scimitar vein and the left atrium, surgical rerouting of the scimitar vein was expected to be difficult. Therefore, after confirmation of insignificant hemodynamic changes by a balloon occlusion test of the scimitar vein, simple ligation of the scimitar vein via video-assisted thoracoscopic surgery, a minimally invasive procedure, was successfully performed.

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11

Fritz, Christian J., Heiko M. Reutter, and Ulrike Herberg. "Scimitar syndrome in a case with VACTERL association." Cardiology in the Young 25, no. 3 (June 6, 2014): 606–9. http://dx.doi.org/10.1017/s1047951114000924.

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AbstractVACTERL association and Scimitar syndrome are rare congenital diseases. In this study, we report on a neonate with prenatal suspicion of VACTERL association and small left-sided cardiac structures, which, only on postnatal angiography, could be revealed to be part of a Scimitar syndrome. As this is the second reported case of VACTERL association and Scimitar syndrome, the presence of Scimitar syndrome should be considered in the prenatal and postnatal evaluation of VACTERL association.

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12

Poncelet, Alain J., Karlien Carbonez, and Jean E. Rubay. "Autologous vascularised pericardial flap tunneling technique in Scimitar syndrome repair with dextrocardia: lessons from the Senning procedure." Cardiology in the Young 31, no. 5 (January 15, 2021): 859–61. http://dx.doi.org/10.1017/s1047951120004928.

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AbstractScimitar syndrome is a rare variant (5%) of partial abnormal pulmonary venous return. Surgery is required when pulmonary overcirculation is present. Following repair, Scimitar vein stenosis occurs in approximately 20%. We applied a variant of the atrial switch technique using autologous pericardial flap in a patient with Scimitar syndrome and dextrocardia. This tunneling technique allowed tension-free anastomosis and minimal Scimitar vein rotation.

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13

Cantinotti, Massimiliano, Raffaele Giordano, and Isabella Spadoni. "Congenitally palliated scimitar syndrome." Cardiology in the Young 25, no. 6 (October 24, 2014): 1218–20. http://dx.doi.org/10.1017/s1047951114001826.

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AbstractWe present a rare case of scimitar syndrome in which the scimitar vessel, collecting all the right pulmonary veins, was stenotic at its junction, with the inferior caval vein and two anomalous vessels, connecting to the same venous collector, draining most of the flow to the left atrium.We arbitrarily defined this rare anatomical variant as a congenitally palliated scimitar syndrome.

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14

Anand, Puneet. "Tetralogy of Fallot with Scimitar syndrome in VACTERL: a very rare association." International Journal of Contemporary Pediatrics 5, no. 1 (December 21, 2017): 269. http://dx.doi.org/10.18203/2349-3291.ijcp20175600.

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The most common congenital cardiac malformation that occurs in VACTERL association is ventricular septal defect. Scimitar syndrome is a very rare congenital anomaly of the heart occurring due to maldevelopment of the lung bud or the pulmonary vascularization during early embryogenesis. The occurrence of Scimitar syndrome in VACTERL and its association with another cardiac congenital anomaly such as Tetralogy of Fallot (TOF) is extremely rare. The association of Tetralogy of Fallot with Scimitar syndrome alters the management strategy. Hereby, a very rare combination of Scimitar syndrome and tetralogy of Fallot in a four-year-old boy with VACTERL is presented, who underwent a successful single-stage surgical correction.

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15

Elder, Robert W., Brian E. Kogon, and Anurag Sahu. "“Double whammy”: anomalous pulmonary and systemic venous drainage in a patient with scimitar syndrome." Cardiology in the Young 23, no. 5 (May 9, 2013): 738–39. http://dx.doi.org/10.1017/s1047951113000553.

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AbstractAnomalously draining right pulmonary veins are expected with scimitar syndrome, but systemic venous abnormalities are rare. We present an unusual case of a female patient with scimitar and an interrupted inferior vena cava.

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16

Basek, I. V., A. A. Benken, V. K. Grebennik, I. K/ Ismail-zade, and E. I. Nikolaichuk. "Partial anomalous drainage of pulmonary venous to the inferior vena cava (scimitar syndrome): the part of radiated methods of research in primary diagnostic and control of surgical treatment." Translational Medicine 7, no. 3 (August 4, 2020): 45–54. http://dx.doi.org/10.18705/2311-4495-2020-7-3-45-54.

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Background. “Scimitar” syndrome is a rare congenital malformation with a frequency of 2 per 100,000 newborns. The syndrome is manifested by complete abnormal drainage of the pulmonary veins of the right lung into the inferior vena cava. According to the literature, a typical symptom of scimitar syndrome can be detected on radiographs in no more than 1/3 of patients. Only complex radiation diagnostics with the inclusion of multispiral computed tomographic angiography allows to diagnose “scimitar” syndrome, determine all its components, clarify the anatomical features and determine the volume and tactics of further cardiac surgery. Objective of the present clinical case is to assess the role of radiation research methods in the primary diagnosis and control of surgical treatment of scimitar syndrome. Materials and methods. A 39-year-old patient with a history of open arterial duct ligation and complaints of fatigue, shortness of breath arising from household loads was examined. According to the results of the chest x-ray and MSCT angiography of the chest organs, “scimitar” syndrome was diagnosed, the patient underwent a two-stage cardiosurgical treatment with the assessment of the results by MSCT angiography. Results. According to the results of radiation studies, the patient revealed a rare congenital malformation — “scimitar” syndrome. Conclusion. MSCT angiography of the chest is a highly informative, minimally invasive diagnostic method for the scimitar syndrome. MSCT angiography of the chest allows you to visually and accurately visualize the type of abnormal drainage, the course and place of the confluence of the collector, the presence of anastomoses with the left heart, which directly affects the definition of tactics for surgical correction of the disease. MSCT angiography of the chest allows you to evaluate the results of surgical treatment.

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17

Bujdák, Juraj, Jiří Vondrák, Jan Matějka, Pavel Král, and Bořivoj Korbel. "Scimitar syndrome - a case report." Cor et Vasa 61, no. 1 (March 21, 2019): 72–75. http://dx.doi.org/10.1016/j.crvasa.2018.01.002.

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18

Hoshino, Yusuke, and Junichi Arai. "Unusual Course of Scimitar Syndrome Preceded by Lung Hypoplasia." Case Reports in Pediatrics 2019 (December 20, 2019): 1–3. http://dx.doi.org/10.1155/2019/8927243.

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In patients with Scimitar syndrome, right pulmonary artery hypoplasia is considered to lead to right lung hypoplasia because of decrease in blood flow. However, there are no reports wherein the change was actually detected. Thus, the exact developmental mechanism of right pulmonary artery hypoplasia and right lung hypoplasia in patients with Scimitar syndrome is unclear. We experienced a case of Scimitar syndrome preceding right lung hypoplasia, and right pulmonary artery hypoplasia gradually revealed with time. We hypothesized that, in our patient, the lung hypoplasia led to pulmonary artery hypoplasia due to decrease in blood flow. If there are no differences in the diameter of the left and right pulmonary artery in patients with Scimitar syndrome at birth, we propose the necessity of careful observation due to the possibility that pulmonary artery hypoplasia may develop in the future.

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19

Lark, Mary, Amanda Cai, Phillip Rideout, David Gregg, Pal Suranyi, Fred A. Crawford, and Valerian L. Fernandes. "Novel Technique of Surgical Management of Scimitar Syndrome." Case Reports in Cardiology 2019 (May 6, 2019): 1–5. http://dx.doi.org/10.1155/2019/6932680.

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Scimitar syndrome is a rare congenital abnormality resulting from right-sided pulmonary venous return to the inferior vena cava rather than to the left atrium. It is usually detected in early childhood with symptoms of recurrent chest infection and finding of pulmonary hypertension due to left to right shunt. We report a case of a 40-year-old woman with scimitar syndrome discovered on chest X-ray during evaluation of recurrent pneumonia. Surgical correction was achieved with a novel technique of using a synthetic graft connecting the scimitar vein across the right atrium to the left atrium along with ligation of the scimitar vein connection to the inferior vena cava. The patient continues to do well 10 years after surgery, and the shunt graft shows good flow on echocardiogram. We present her clinical and imaging data and details of the surgical technique along with a brief review of surgical literature.

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20

Taylor, Nikki P., Zsofia Long, Michael Ma, and Alisa Arunamata. "Recurrent fibrovascular granulation on PhotoFix® bovine pericardium causing systemic and pulmonary venous obstruction after repair of scimitar syndrome." Cardiology in the Young 31, no. 5 (March 8, 2021): 829–30. http://dx.doi.org/10.1017/s1047951121000822.

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AbstractA young adult with late diagnosis of scimitar syndrome underwent infradiaphragmatic baffling of the scimitar vein to left atrium through an intra-atrial tunnel using PhotoFix® bovine pericardium with recurrent extensive fibrovascular granulation of the patch causing pulmonary and systemic venous obstruction leading to eventual explantation of the bovine pericardium.

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21

Yoo, Shi-Joon, Abdulmajeed Al-Otay, and Paul Babyn. "The relationship between scimitar syndrome, so-called scimitar variant, meandering right pulmonary vein, horseshoe lung and pulmonary arterial sling." Cardiology in the Young 16, no. 3 (May 26, 2006): 300–304. http://dx.doi.org/10.1017/s1047951106000461.

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We report a case in which a meandering right pulmonary vein connecting to the left atrium is associated with hypoplasia of the right lung, horseshoe lung, abnormal pulmonary lobation, and abnormal branching of the pulmonary arteries. We discuss its relationship to the so-called scimitar variant, and to the scimitar syndrome itself.

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22

Louhichi, Marouane, Touhami Khorchani, Douglas Eifler, Maria Eifler, Makenna Orton, Kamel Dadi, Ali Zaydi, Mohsen Jarray, and Mohsen Chammem. "Modelling habitat suitability of reintroduced scimitar-horned oryx (Oryx dammah) in Sidi Toui National Park, Tunisia." JOURNAL OF OASIS AGRICULTURE AND SUSTAINABLE DEVELOPMENT 6, no. 02 (June 7, 2024): 1–13. http://dx.doi.org/10.56027/joasd.162024.

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Reintroducing endangered species into their restored habitats is a significant aspect of conservation biology. The scimitar-horned oryx (Oryx dammah), one of the most critically endangered antelopes worldwide, was reintroduced into several protected areas in Tunisia. Understanding their habitat requirements within micro-level ecosystems is crucial for developing effective management plans to aid in species recovery. Using information-theoretic and multimodel inference (MMI) techniques, we evaluated the impact of habitat and management characteristics on the distribution of the scimitar-horned oryx in Tunisia's Sidi Toui National Park during different seasons, from June 2020 – May 2022. Our analyses, using regression coefficients and selection probabilities, revealed that factors influencing habitat suitability varied seasonally for the scimitar-horned oryx. However, the presence of grasses emerged as the most consistent indicator of their occurrence throughout the year. The strong fit of models to the data was confirmed by Receiver Operating Characteristic (ROC) plots, which indicated an Area Under the Curve (AUC) > 0.9. The study has significant implications for developing practical habitat management plans for the scimitar-horned oryx in Sidi Toui National Park.

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23

Pekcan, Sevgi, AyselBurcu Palandökenlier, and Tamer Baysal. "Scimitar Syndrome." Pediatric Dimensions 1, no. 1 (2016): 19–21. http://dx.doi.org/10.15761/pd.1000104.

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24

Kejriwal, G. S., CH Madhavi, and S. N. Sahu. "Scimitar syndrome." Bangladesh Journal of Medical Science 14, no. 1 (January 12, 2015): 103–5. http://dx.doi.org/10.3329/bjms.v14i1.21576.

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A female child of age five attended our institution in Jan 2006 with repeated upper respiratory infection. Plain skiagram and CT examinations confirmed the case to be a Scimitar syndrome. DOI: http://dx.doi.org/10.3329/bjms.v14i1.21576 Bangladesh Journal of Medical Science Vol.14(1) 2015 p.103-105

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25

Dennehy, William, and Eric M. Neverman. "Scimitar syndrome." Journal of Osteopathic Medicine 121, no. 9 (June 22, 2021): 771–72. http://dx.doi.org/10.1515/jom-2021-0142.

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26

Ielasi, Alfonso, Azeem Latib, Eustachio Agricola, Matteo Montorfano, and Antonio Colombo. "Scimitar syndrome." Journal of Cardiovascular Medicine 12, no. 3 (March 2011): 176–77. http://dx.doi.org/10.2459/jcm.0b013e328332f3e2.

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27

Ali, Yehia Z., and Crystal Bonnichsen. "Scimitar Syndrome." European Heart Journal - Cardiovascular Imaging 21, no. 8 (May 13, 2020): 939. http://dx.doi.org/10.1093/ehjci/jeaa061.

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28

Tavare, A. N., and P. Wylie. "Scimitar syndrome." QJM 107, no. 6 (October 15, 2013): 477. http://dx.doi.org/10.1093/qjmed/hct207.

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29

Gudjonsson, Ulf, and John W. Brown. "Scimitar Syndrome." Seminars in Thoracic and Cardiovascular Surgery: Pediatric Cardiac Surgery Annual 9, no. 1 (January 2006): 56–62. http://dx.doi.org/10.1053/j.pcsu.2006.02.011.

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30

Sweeney, W. Brian. "Scimitar Syndrome." Military Medicine 153, no. 4 (April 1, 1988): 209–12. http://dx.doi.org/10.1093/milmed/153.4.209.

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31

Ferrari, Victor A., Muredach P. Reilly, Leon Axel, and Martin G. St John Sutton. "Scimitar Syndrome." Circulation 98, no. 15 (October 13, 1998): 1583–84. http://dx.doi.org/10.1161/01.cir.98.15.1583.

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32

Harre, Julia, and John V. Forrest. "Scimitar Syndrome." Chest 98, no. 2 (August 1990): 510–11. http://dx.doi.org/10.1378/chest.98.2.510-b.

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33

Georghiou, G. P. "Scimitar syndrome." Heart 91, no. 12 (December 1, 2005): 1589. http://dx.doi.org/10.1136/hrt.2005.062877.

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34

Ho, Christopher B. "Scimitar syndrome." Journal of Emergency Medicine 21, no. 3 (October 2001): 279–81. http://dx.doi.org/10.1016/s0736-4679(01)00384-5.

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35

Mannes, Gregor P. M., and Pieter E. Postmus. "Scimitar Syndrome." Chest 98, no. 2 (August 1990): 511. http://dx.doi.org/10.1016/s0012-3692(16)31696-8.

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36

Suri, Deepti, Kushaljit S. Sodhi, Jayashree Muralidharan, Rohit Manoj, and Sunit Singhi. "Scimitar Syndrome." Pediatric Emergency Care 24, no. 3 (March 2008): 164–66. http://dx.doi.org/10.1097/pec.0b013e3181668aff.

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37

Rai, SP, J. D'Souza, and P. Saxena. "Scimitar syndrome." Medical Journal Armed Forces India 67, no. 3 (July 2011): 299. http://dx.doi.org/10.1016/s0377-1237(11)60070-1.

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38

Riedel, M., J. Hausleiter, and S. Martinoff. "Scimitar syndrome." Lancet 363, no. 9406 (January 2004): 356. http://dx.doi.org/10.1016/s0140-6736(04)15435-4.

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39

Elsallabi, Osama, Aiman Smer, Bradley DeVrieze, and Gopi Sirineni. "Scimitar Syndrome." Journal of General Internal Medicine 31, no. 2 (May 5, 2015): 253–54. http://dx.doi.org/10.1007/s11606-015-3358-7.

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40

Rokade, Muktachand L., R. V. Rananavare, Devdas S. Shetty, and Shenaz Saifi. "Scimitar syndrome." Indian Journal of Pediatrics 72, no. 3 (March 2005): 245–47. http://dx.doi.org/10.1007/bf02859267.

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41

Sehgal, Arvind, and Alison Loughran-Fowlds. "Scimitar syndrome." Indian Journal of Pediatrics 72, no. 3 (March 2005): 249–51. http://dx.doi.org/10.1007/bf02859268.

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42

Pearl, William. "Scimitar variant." Pediatric Cardiology 8, no. 2 (June 1987): 139–41. http://dx.doi.org/10.1007/bf02079472.

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43

Infaaq, M. L. M., M. Fernando, S. Perera, and D. T. K. Gamage. "Scimitar syndrome." Sri Lanka Journal of Child Health 42, no. 2 (June 1, 2013): 103. http://dx.doi.org/10.4038/sljch.v42i2.5635.

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44

Vida, Vladimiro L., Massimo A. Padalino, Giovanna Boccuzzo, Erjon Tarja, Hakan Berggren, Thierry Carrel, Sertaç Çiçek, et al. "Scimitar Syndrome." Circulation 122, no. 12 (September 21, 2010): 1159–66. http://dx.doi.org/10.1161/circulationaha.109.926204.

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45

Nazarian, John, Jeffrey P. Kanne, and Prabhakar Rajiah. "Scimitar Sign." Journal of Thoracic Imaging 28, no. 4 (July 2013): W61. http://dx.doi.org/10.1097/rti.0b013e318292043e.

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46

Navas Lobato, Miguel A., Ángel Sánchez-Recalde, Roberto Martin Reyes, Pilar Lurueña Lobo, Jose M. Oliver Ruiz, Montse Bret Zurita, and Jose L. López Sendón. "Scimitar Syndrome." Clinical Cardiology 32, no. 7 (July 2009): E15—E16. http://dx.doi.org/10.1002/clc.20261.

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47

Bauch, Alexandra, Kyong-Jin Lee, and Shi-Joon Yoo. "Complete congenital obstruction of a scimitar vein in an infant with severe respiratory failure." Cardiology in the Young 19, no. 5 (August 12, 2009): 524–26. http://dx.doi.org/10.1017/s1047951109990825.

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AbstractWe report an infant of 3 1/2 months with complete obstruction of the venous component of the scimitar syndrome, a large atrial septal defect within the oval fossa, a common left pulmonary vein, and pulmonary hypertension. To the best of our knowledge, ours is the first description of complete congenital obstruction of a scimitar vein.

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48

Saltik, Levent, Sezen Ugan Atik, and Helen Bornaun. "Transcatheter correction of Scimitar syndrome: occlusion of abnormal pulmonary venous drainage and vascular supply in an infant." Cardiology in the Young 27, no. 8 (May 16, 2017): 1627–29. http://dx.doi.org/10.1017/s1047951117000750.

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AbstractTreatment of Scimitar syndrome is usually surgical; however, if there is “dual drainage” – that is, one to the inferior caval vein and the other to the left atrium – it is possible to successfully treat this anomaly via a less-invasive transcatheter approach. We report a case of Scimitar syndrome in a 21-month-old, male infant successfully treated with transcatheter embolisation.

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49

Bartram, Ulrike, Stella Van Praagh, John F. Keane, Peter Lang, Mary E. van der Velde, and Richard Van Praagh. "Mitral and Aortic Atresia Associated with Hypoplastic Right Lung, Crossover Segment of Right Lower Lobe, and Anomalous Scimitar-like Right Pulmonary Venous Connection with Inferior Vena Cava: Clinical, Angiocardiographic, and Autopsy Findings in a Rare Case." Pediatric and Developmental Pathology 1, no. 5 (September 1998): 413–19. http://dx.doi.org/10.1007/s100249900056.

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A newborn female infant was found to have a unique and previously unreported group of anomalies: ( 1) mitral and aortic atresia with a highly obstructive atrial septum; ( 2) hypoplasia of the right lung with a crossover segment involving the right lower lobe; ( 3) normally connected pulmonary veins, two from the left lung and one from the right; and ( 4) a large anomalous branch of the right pulmonary vein of scimitar configuration that anastomosed with the normally connected right pulmonary vein and with the inferior vena cava (IVC). The scimitar vein appeared obstructed at its junction with the right pulmonary vein and at its junction with the inferior vena cava within the hepatic parenchyma. To our knowledge, this is the first report of a scimitar-like vein coexisting with mitral and aortic atresia and connecting both with the right pulmonary vein and with the inferior vena cava. The highly obstructed left atrium was partially decompressed by retrograde blood flow via the normally connected right pulmonary vein to the anomalous scimitar venous pathway and thence to the inferior vena cava via a pulmonary-to-IVC collateral vein.

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50

Alabi, Fortune O., Fred Umeh, Maximo Lama, and Francis G. Christian. "Uncommon Cause of Paradoxical Embolism in a Case of Scimitar Syndrome." Case Reports in Medicine 2013 (2013): 1–3. http://dx.doi.org/10.1155/2013/352128.

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Scimitar syndrome, a rare congenital cardiopulmonary condition, presents in both pediatric and adult populations as an anomalous pulmonary venous return of most of the right lung to the inferior vena cava. Recently, asymptomatic adult cases have been diagnosed with advances in imaging studies. We report the case of an asymptomatic 43-year-old male, with a complex variant scimitar syndrome diagnosed by computed tomographic angiography.

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