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Ginecología y Obstetricia de México

Federación Mexicana de Ginecología y Obstetricia, A.C.
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2014, Number 12

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Ginecol Obstet Mex 2014; 82 (12)

Ductus arteriosus aneurysm. Case report and review of the literature

Juárez-García L, López-Rioja MJ, Erdmenger-Orellana J, Leis-Márquez MT, Kably-Ambe A
Full text How to cite this article

Language: Spanish
References: 11
Page: 839-842
PDF size: 375.87 Kb.


Key words:

aneurysm, arterious duct, pregnancy.

ABSTRACT

The saccular or fusiform dilatation of the ductus arteriosus is called aneurysm (DAA). It is diagnosed in the second trimester during a structural ultrasound. Even though the reported incidence is 2.2%, it remains infrequent, because it is not searched routinely.
The pathogenesis is uncertain, resulting from an increase on the circulating blood volume thus in the cardiac afterload, associated to a thinning of the vessel wall, for an inadequate intima development.
Ductus arteriosus aneurysm can be classified according by their diameter as small (‹7mm.) and large (≥8mm). The smaller commonly closes spontaneously in 70% of the cases, unlike the larger one, they are associate in a greater number of complications, such as thrombosis, embolism, infection, compression effects of adjacent structures and spontaneous rupture. The absence of spontaneous closure, according to the symptoms and possible complications, a neonatal surgical closure should be considered.
We report a case of a 35 year old patient, diagnose on the 35 week pregnancy, a ductus arteriosus aneurysm by ultrasound with an image of the three vessels performed communicating, saccular dilatation of 7-8 mm. and a turbulent Doppler flow.


REFERENCES

  1. Murki S, Deshbhatla S, Sharma D, et al. Congenital ductus arteriosus aneurysm: an unusual cause of transient neonatal hypertension. BMJ Case Rep 2014;5:2014.

  2. Jeong S, Jeung C. Case Report: A Case of Isolated Congenital Ductus Arteriosus Aneurysm Detected by Fetal Echocardiography at 38 Weeks of Gestation. J Clin Ultrasound 2011;39:530-533.

  3. Singh J, Kobayashi D, Chen M, et al. Neonatal systemic thromboembolism secondary to ductus arteriosus aneurysm and patent foramen ovale. Congenit Heart Dis 2013; 8:5-9.

  4. Jan S, Fu Y, Chan S, et al. Ductus arteriosus aneurysm with persistent left superior vena cava in a neonate: a “four-star sign” on echocardiography. Int J Cardiol 2013;31:49-50.

  5. Jackson C, Sandor G, Lim K, et. al. Diagnosis of fetal ductus arteriosus aneurysm: importance of the three-vessel view. Ultrasound Obstet Gynecol 2005;26:57-62.

  6. Schneider C, McCrindle W, Carvalho J, et al. Development of Z-scores for fetal cardiac dimensions from echocardiography. Ultrasound Obstet Gynecol 2005;26:599-605.

  7. Tseng J, Jan S. Fetal echocardiographic diagnosis of isolated ductus arteriosus aneurysm: a longitudinal study from 32 weeks of gestation to term. Ultrasound Obstet Gynecol 2005;26:50-56.

  8. Sheng-Ling J, Betau H, Yun-Ching F, et al. Isolated Neonatal Ductus Arteriosus Aneurysm. ACC 2002;39:342–347.

  9. Jung, H. A case of fetal ductus arteriosus aneurysm. Ultrasound Obstet Gynecol 2013;42:120-121.

  10. Dyamenahalli U, Smallhorn J, Geva T, et al. Isolated ductus arteriosus aneurysm in the fetus and infant: a multi-institutional experience. J Am Coll Cardiol 2000;36:262-269.

  11. Sheridan R, Michelfelder E, Choe K, et al. Ductus arteriosus aneurysm with massive thrombosis of pulmonary artery and fetal hydrops. Pediatr Dev Pathol 2012;15:79-85.




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Ginecol Obstet Mex. 2014;82