Five cases of hypoplasia of the descending thoracic and/or abdominal aorta as a rare cause of hypertension are presented. Similarities and dissimilarities between this lesion and classical coarctation of the aorta are discussed. Man agement of the resulting hypertension is usually medical, as surgical therapy is extremely difficult due to the diffuse involvement of the entire aorta and its branches.
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References
1.
Ben-Shoshan M., Rossi NP, Korns ME: Coarctation of the abdominal aorta. Arch Path95:221-225, 1973.
2.
Onat T., Zeren E.: Coarctation of the abdominal aorta. Review of 91 cases. Cardiologia54:140-157, 1969.
3.
Siassi B., Klyman G., Emmanoulides GC: Hypoplasia of the abdominal aorta associated with the rubella syndrome. Am J Dis Chil120:476-479, 1970.
4.
Limbacher JP , Hill ME, Janicki PC: Hypoplasia of the abdominal aorta associated with rubella syndrome. South Med J72:617-619, 1979.
5.
Bliddal J., Dupont B., Melchior JC, Ottesen OE: Coarctation of the aorta with multiple artery anomalies in idiopathic hypercalcemia of infancy. Acta Paediatr Scand58:632-637, 1969.
6.
Schurch W., Messerli FH, Genest J., et al: Arterial hypertension and neurofibromatosis: Renal artery stenosis and coarctation of abdominal aorta. Can Med Assoc J113:879-885, 1975.