Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-14T05:38:38.675Z Has data issue: false hasContentIssue false

Horseshoe lung associated with anomalous pulmonary venous connection without pulmonary hypoplasia

Published online by Cambridge University Press:  19 August 2008

Antonio Corno
Affiliation:
From the Department of Pediatric Cardiology and Cardiac Surgery, Centro E. Malan, Ospedale “San Donato,”, San Donato Milanese
Luca Rosti*
Affiliation:
From the Department of Pediatric Cardiology and Cardiac Surgery, Centro E. Malan, Ospedale “San Donato,”, San Donato Milanese
Ivan Machado
Affiliation:
From the Department of Pediatric Cardiology and Cardiac Surgery, Centro E. Malan, Ospedale “San Donato,”, San Donato Milanese
*
Dr. Luca Rosti, Ospedale “San Donato,” via Morandi 30, 20097 San Donato Milanese (MI), Italy. Tel. 39-2-52774511; Fax. 39-2-52747 17.

Summary

Horseshoe lung is an exceedingly rare congenital malformation, characterized by unilateral pulmonary hypoplasia together with a midline isthmus producing fusion of the tissues of the lower lobes. It is frequently associated with other cardiac and extracardiac anomalies. We report an infant with a variant of the horseshoe lung with partial anomalous venous connection of intracardiac type, ventricular septal defect, and persistent left superior caval vein. There was no pulmonary hypoplasia.

Type
Brief Reports
Copyright
Copyright © Cambridge University Press 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Hawass, ND, Badawi, MG, Al-Muzrakchi, AM, Al-Samarai, Al, Jawad, AJ, Abdullah, MA, Bahakim, H.Horseshoe lung: differential diagnosis. Pediatr Radiol 1990; 20: 580584.Google Scholar
Figs, FH, Yoo, SJ, Burrows, PE, Turner-Gomes, S, Freedom, RM.Horseshoe lung—a case report with unusual bronchial and pleural anomalies and a proposed new classification. Pediatr Radiol 1993; 23: 4447.Google Scholar
Freedom, RM, Burrows, PE, Moes, CAF.“Horseshoe” lung: report of five new cases. Am J Radiol 1986; 146: 211215.Google Scholar
Dische, MR, Teixeira, ML, Winchester, PH, Engle, MA. Horseshoe lung associated with a variant of—the “scimitar” syndrome. Brit Heart J 1974; 36: 617620.Google Scholar
Ersoz, A, Soncul, H, Gokgoz, L, Kalaycioglu, S, Tunaoglu, S, Kaptanoglu, M, Yener, A.Horseshoe lung with left lung hypoplasia. Thorax 1992; 47: 205206.Google Scholar
Obregon, MG, Giannotti, A, Digilio, MC, Barbuti, D, Mingarelli, R, Dallapiccola, B.Horseshoe lung: an additional component of the Vater association. Pediatr Radiol 1992; 22: 158.Google Scholar
Takeda, K, Kato, N, Nakagawa, T, Aoki, K, Matsuda, A.Horseshoe lung without respiratory distress. Pediatr Radiol 1990; 20: 604.Google Scholar
Hassberg, D, Steil, E, Sieverding, L, Rosendahl, W.Kombination von Scimitar-Syndrome und Hufeisenlunge. Em seltener aber typischer Befund—Fallbericht und Literaturubersicht. KIin Padiatr 1992; 204: 434443.Google Scholar
Cerruti, MM, Marmolejos, F, Cacciarelli, T.Bilateral intralobar pulmonary sequestration with horseshoe lung. Ann Thorac Surg 1993; 55: 509510.Google Scholar
Frank, JL, Poole, CA, Rosas, G.Horseshoe lung: clinical, pathologic, and radiologic features and a new plain film finding. Am J Radiol 1986; 146: 217226.Google Scholar