Multiple Cutaneous Hemangiomas and Coarctation of the Aorta With Right Aortic Arch

PEDIATRICS ◽  
1988 ◽  
Vol 81 (5) ◽  
pp. 707-710
Author(s):  
LOÏC VAILLANT ◽  
GÉRARD LORETTE ◽  
ALAIN CHANTEPIE ◽  
MICHEL MARCHAND ◽  
DANIEL ALISON ◽  
...  

Strawberry hemangiomas are the most common congenital vascular malformation seen in infants. Usually, they appear as a raised bright or purplish red lobulated tumor with well-defined borders and capillaries protruding from its surface. They are not present at birth. They develop during the first weeks of life, grow rapidly during the first 6 months, remain stationary for awhile, and then undergo complete or partial involution and resolution without treatment. Usually, these hemangiomas are solitary or in small number1 and are not associated with congenital anomalies. We report a case of strawberry hemangiomas that is unusual because of the multiplicity and extension associated with laryngeal hemangioma and coarctation with right aortic arch.

2000 ◽  
Vol 9 (2) ◽  
pp. 103-106 ◽  
Author(s):  
Giangiorgio Crisponi ◽  
Andrea Raffaele Marras ◽  
Adriano Corrias ◽  
Luigi Memo ◽  
Marino Gorinati ◽  
...  

2013 ◽  
Vol 17 (2) ◽  
pp. 444-446 ◽  
Author(s):  
Fabrizio Gandolfo ◽  
Sonia B. Albanese ◽  
Aurelio D.M. Secinaro ◽  
Adriano Carotti

2021 ◽  
pp. 1-3
Author(s):  
Kei Kobayashi ◽  
Gen Harada ◽  
Takeshi Shinkawa

Abstract Right aortic arch in association with coarctation of the aorta and vascular ring is a rare anatomy. We present an infant with chromosome 22q11.2 deletion, who had the right aortic arch with retroesophageal aberrant left subclavian artery and left internal carotid artery. The left external carotid artery and right common carotid artery originated together from the ascending aorta as a bovine branch. The infant also had severe coarctation, which was prostaglandin dependent.


2006 ◽  
Vol 27 (5) ◽  
pp. 621-623 ◽  
Author(s):  
Shelli Bein ◽  
Ziad Saba ◽  
Hitendra Patel ◽  
Olaf Reinhartz ◽  
Frank L. Hanley

2003 ◽  
Vol 29 (5) ◽  
pp. S62
Author(s):  
B. Yi ◽  
J. Cho ◽  
Y. Lee ◽  
H. Lee ◽  
J. Ryu ◽  
...  

1997 ◽  
Vol 7 (4) ◽  
pp. 458-461 ◽  
Author(s):  
Shinichi Tsubata ◽  
Fukiko Ichida ◽  
Toshio Miyawaki

AbstractWe report the first infant case with coarctation of the aorta and mirror image right aortic arch, who presented with severe myocardial dysfunction and underwent successful balloon angioplasty for relief of coarctation, avoiding anesthetic and surgical risk. A follow-up cardiac cathetelization revealed no residual pressure gradient and continued angiographic improvement with excellent restoration in left ventricular function.


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