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The Eisenmenger malformation: a morphologic study

Published online by Cambridge University Press:  17 February 2015

Angelo Restivo
Affiliation:
Department of Radiology, Oncology and Pathological Anatomy, Museum of Pathological Anatomy, Sapienza University of Rome, Rome, Italy
Cira R. T. di Gioia*
Affiliation:
Department of Radiology, Oncology and Pathological Anatomy, Museum of Pathological Anatomy, Sapienza University of Rome, Rome, Italy
Robert H. Anderson
Affiliation:
Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom
Raffaella Carletti
Affiliation:
Department of Radiology, Oncology and Pathological Anatomy, Museum of Pathological Anatomy, Sapienza University of Rome, Rome, Italy
Pietro Gallo
Affiliation:
Department of Radiology, Oncology and Pathological Anatomy, Museum of Pathological Anatomy, Sapienza University of Rome, Rome, Italy
*
Correspondence to: Prof. C. R. T. di Gioia, Dipartimento di Scienze Radiologiche, Oncologiche e, Anatomopatologiche, Sezione di Anatomia Patologica, Sapienza Università di Roma, Policlinico Umberto I, Viale Regina Margherita 324, 00161 Rome, Italy. Tel: +39 064 997 3329; Fax: +39 064 997 3329; E-mail: [email protected]

Abstract

We studied 11 autopsied cases of the Eisenmenger malformation, comparing the findings with 11 hearts with intact ventricular septal structures, and nine hearts having perimembranous ventricular septal defects in the absence of aortic overriding. We found variable lengths for the subpulmonary infundibulum in the hearts with Eisenmenger defects. It was well developed in three hearts, of intermediate length in seven, and very short in one of the specimens. The muscular outlet septum was also of variable length compared with the free-standing subpulmonary infundibular sleeve. Except for one, all hearts had fibrous continuity between the aortic and tricuspid valvar leaflets, such that the ventricular septal defect was then perimembranous. In the remaining case, there was a completely subaortic muscular infundibulum, with the ventricular septal defect showing only muscular borders. The medial papillary muscle was absent in the majority of cases, but was well formed in three hearts, all with relatively short muscular outlet septums. We identified mild, intermediate, and severe degrees of rightward rotation of the aortic valve, and these findings correlated with the extent of aortic valvar overriding. In nine of the 11 hearts, the ventriculo-arterial connections were concordant, but there was double-outlet from the right ventricle in the other two specimens. Based on our anatomic and morphometric observations, we conclude that the hearts we have defined as having Eisenmenger defects show marked individual variation in their specific phenotypic anatomy.

Type
Original Articles
Copyright
© Cambridge University Press 2015 

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References

1. Eisenmenger, V. Die angeborenen defecte der kammerscheidewand des herzens. Ztschr F Klin Med 1898; 32 (Suppl): 156.Google Scholar
2. Baumgartner, EA, Abbott, ME. Interventricular septal defect with dextroposition of the aorta and dilatation of the pulmonary artery (Eisenmenger complex) terminating by cerebral abscess. Am J Med Sci 1929; 117: 639645.Google Scholar
3. Abbott, ME. Discussion. Int Assoc Med Museums Bull 1937; 17: 90111.Google Scholar
4. Wood, P. The Eisenmenger syndrome or pulmonary hypertension with reversed central shunt (The Croonian Lectures). Br Med J 1958; 2: 757762.CrossRefGoogle ScholarPubMed
5. Van Mierop, LHS, Wiglesworth, FW. Anomalies due to faulty transfer of the posterior great artery. Am J Cardiol 1963; 12: 226232.CrossRefGoogle Scholar
6. Altshuler, G. The ventricular septal defect. Developmental significance in conotruncal and aortic arch anomalies. Am J Dis Child 1970; 119: 407415.CrossRefGoogle ScholarPubMed
7. Goor, DA, Lillehei, CW, Edwards, JE. Ventricular septal defects and pulmonic stenosis with and without dextroposition. Anatomic features and embryologic implications. Chest 1971; 60: 117128.CrossRefGoogle ScholarPubMed
8. Oppenheimer-Dekker, A, Gittenberger-de Groot, AC, Bartelings, MM, Wenink, AC, Moene, R, van der Harten, JJ. Abnormal architecture of the ventricles in hearts with an overriding aortic valve and a perimembranous ventricular septal defect (“Eisenmenger VSD”). Int J Cardiol 1985; 9: 341355.Google Scholar
9. Chen, H, Xu, Z, Wang, S, Shen, J, Zhang, Z, Hong, H. Eisenmenger ventricular septal defect: classification, morphology, and indications for surgery. Pediatr Cardiol 2011; 32: 1723.Google Scholar
10. Gasul, BM, Dillon, RE, Vrla, V, Hait, G. Ventricular septal defects. Their natural transformation into those with infundibular stenosis or into the cyanotic or noncyanotic type of tetralogy of Fallot. J Am Med Assoc 1957; 164: 847853.CrossRefGoogle ScholarPubMed
11. Fukuda, T, Suzuki, T, Ito, T. Clinical and morphologic features of perimembranous ventricular septal defect with overriding of the aorta – the so-called Eisenmenger ventricular septal defect. A study making comparisons with tetralogy of Fallot and perimembranous ventricular defect without aortic overriding. Cardiol Young 2000; 103: 343352.Google Scholar
12. Bozok, S, Kestelli, M, Ilhan, G, et al. Tips and pearls for “true” dextroposition of the aorta in tetralogy of Fallot. Cardiol Young 2013; 23: 377380.Google Scholar
13. Anderson, RH. Truth relative to aortic overriding. Cardiol Young 2014; 24: 184185.CrossRefGoogle ScholarPubMed
14. Restivo, A, Unolt, M, Putotto, C, Marino, B. Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects. Anat Rec 2013; 296: 559563.Google Scholar
15. Anderson, RH. How best can we define double outlet right ventricle when describing congenitally malformed hearts? Anat Rec 2013; 296: 993994.CrossRefGoogle ScholarPubMed
16. Restivo, A, Smith, A, Wilkinson, JL, Anderson, RH. The medial papillary muscle complex and its related septomarginal trabeculation. A normal anatomical study on human hearts. J Anat 1989; 163: 231242.Google Scholar
17. Anderson, RH, Spicer, DE, Giroud, JM, Mohun, TJ. Tetralogy of Fallot: nosological, morphological, and morphogenetic considerations. Cardiol Young 2013; 23: 858866.Google Scholar
18. Becker, AE, Connor, M, Anderson, RH. Tetralogy of Fallot: a morphometric and geometric study. Am J Cardiol 1975; 35: 402412.Google Scholar
19. Dickinson, DF, Wilkinson, JL, Smith, A, Hamilton, DI, Anderson, RH. Variations in the morphology of the ventricular septal defect and disposition of the atrioventricular conduction tissues in tetralogy of Fallot. Thorac Cardiovasc Surg 1982; 30: 243249.Google Scholar
20. Rosenquist, GC, Clark, EB, Sweeney, LJ, McAllister, HA. The normal spectrum of mitral and aortic valve discontinuity. Circulation 1976; 54: 298301.Google Scholar
21. Isaaz, K, Cloez, JL, Marcon, F, Worms, AM, Pernot, C. Is the aorta truly dextroposed in tetralogy of Fallot? A two dimensional echocardiographic answer. Circulation 1986; 73: 892899.Google Scholar