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A practical approach to the examination of the congenitally malformed heart at autopsy


Authors: Ondřej Fabián 1;  Roman Gebauer 2
Authors‘ workplace: Ústav patologie a molekulární medicíny 2. LF UK a FN Motol, Praha 1;  Dětské kardiocentrum 2. LF UK a FN Motol, Praha 2
Published in: Čes.-slov. Patol., 55, 2019, No. 4, p. 202-208
Category: Reviews Article

Overview

Congenital heart defects (CHD) represent the most frequent type of the heart disease in childhood, with incidence up to 1 % of all live-born children. Despite the improving echocardiographic diagnostics, part of CHD remains undiagnosed and can manifest in the later age or may be the cause of the early abortion. On the other hand, some foetuses with prenatally diagnosed severe CHD may be recommended to interruption. Therefore, each pathologist can encounter a malformed heart at the autopsy. Despite the current quality of the echocardiography, the macroscopic assessment of the heart by the pathologist is still considered the best method for evaluation of the structural heart disease. Knowledge of the basic pathologic anatomy thus remains an important prerequisite for adequately performed paediatric autopsy.

Keywords:

pathology – congenital heart disease – sequential segmental analysis


Sources

1. Krasuski RA, Bashore TM. Congenital Heart Disease Epidemiology in the United States. Circulation 2016; 134(2): 110-113.

2. Ernst LM. A pathologists perspective on the perinatal autopsy. Semin Perinatol 2015; 39(1): 55–63.

3. Taylor GP, Faye-Petersen OM, Ernst L et al. Small patients, complex challenging cases: a reappraisal of the professional efforts in perinatal autopsies. Arch Pathol Lab Med 2014; 138(7): 865-868.

4. Thiene G, Veinot JP, Angelini A et al. AECVP and SCVP 2009 recommendations for training in cardiovascular pathology. Cardiovasc Pathol 2010; 19(3): 129-135.

5. Anderson RH, Shirali G. Sequential segmental analysis. Ann Pediatr Cardiol 2009; 2(1): 24–35.

6. Craatz S, Künzel E, Spanel-Borowski K. Classification of a collection of malformed human hearts: practical experience in the use of sequential segmental analysis. Pediatr Cardiol 2002; 23(5): 483–490.

7. Devine WA, Debich DE, Anderson RH. Dissection of congenitally malformed hearts, with comments on the value of sequential segmental analysis. Pediatr Pathol 1991;11(2): 235–259.

8. Anderson RH, Ho SY. Continuing Medical Education. Sequential segmental analysis - description and catergorization for the millenium. Cardiol Young 1997; 7: 98-116.

9. Khong TY, Malcombson RDG. Keelings Fetal and Neonatal Pathology (5th edn). Switzerland: Springer; 2015: 486-488.

10. Erickson LK. An Approach to the examination of the fetal congenitally malformed heart at autopsy. J Fetal Med 2015; 2(3): 135-141.

11. Arey JB. Cardiovascular pathology in infants and children. Philadelphia: WB Saunders Company; 1984: 77-111, 204–217.

12. DeLisle G, Ando M, Calder AL et al. Total anomalous pulmonary venous connection: Report of 93 autopsied cases with emphasis on diagnostic and surgical considerations. Am Heart J 1976; 91(1): 99–122.

13. Jores L. Die Konservirung anatomischer Präparate in Blutfarbe mittelst Formalin. Centralbl F Allgemeine Path Und Path Anat 1896; 7: 134.

14. Cain MA, Guidi CB, Steffensen T, Whiteman VE, Gilbert-Barness E, Johnson DR. Postmortem ultrasonography of the macerated fetus complements autopsy following in utero fetal demise. Pediatr Dev Pathol 2014; 17(3): 217–220.

15. Arthurs OJ, Thayyil S, Olsen OE et al. Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children. Eur Radiol 2014; 24(11): 2876–2884.

16. Hagen PT, Scholz DG, Edwards WD. Incidence and size of patent oval foramen during the first decades of life; an autopsy study of 965 normal hearts. Mayo Clin Proc 1984; 59(1): 1489–1494.

17. Fisher DC, Fisher EA, Budd JH et al. The incidence of patent oval foramen in 1,000 consecutive patients. A contrast transesophageal echocardiography study. Chest 1995; 107(6): 1504–1509.

18. Ferreira Martins JD, Anderson RH. The anatomy of interatrial communications - what does the interventionist need to know? Cardiol Young 2000; 10(5): 464-473.

19. Al Zaghal AM, Li J, Anderson RH et al. Anatomic criteria for the diagnosis of sinus venosus defects. Heart 1997; 78(3): 298–304.

20. Lee ME, Sade RM. Coronary sinus septal defect. Surgical considerations. J Thorac Cardiovasc Surg 1979; 78(4): 563–569.

21. Goyal SK, Punnam SR, Verma G, Ruberg FL. Persistent left superior vena cava: a case report and review of literature. Cardiovasc Ultrasound 2008; 6: 50.

22. Anderson RH, Lennox CC, Zuberbuhler JR. The morphology of ventricular septal defects. Perspect Pediatr Pathol 1984; 8(3): 235–268.

23. Soto B, Becker AE, Moulaert AJ, Lie JT, Anderson RH. Classification of ventricular septal defects. Br Heart J 1980; 43(3): 332-343.

24. Anderson RH, Wilcox BR. The surgical anatomy of ventricular septal defect. J Card Surg 1992; 7(1): 17-35.

25. Becker AE, Anderson RH. Atrioventricular septal defects. What’s in a name? J Thorac Cardiovasc Surg 1982; 83(3): 461–469.

26. Anderson RH, Ho SY, Falcao S, Daliento L, Rigby ML. The diagnostic features of atrioventricular septal defect with common atrioventricular junction. Cardiol Young 1998; 8(1): 33-49.

27. Ebels T, Meijboom EJ, Anderson RH et al. Anatomic and functional “obstruction” of the outflow tract in atrioventricular septal defects with separate valve orifices (“ostium primum atrial septal defect”): a echocardiographic study. Am J Cardiol 1984; 54(7): 843-847.

28. Sigfùsson G, Ettedgui JA, Silverman NH, Anderson RH. Is a cleft in the anterior leaflet of an otherwise normal mitral valve an atrioventricular canal malformation? J Am Coll Cardiol 1995; 26(2): 508-515.

29. Espinola-Zavaleta N, Muñoz-Castellanos L, Kuri-Nivón M, Keirns C. Understanding atrioventricular septal defect: anatomoechocardiographic correlation. Cardiovasc Ultrasound 2008: 6: 33.

30. Anderson RH, Allwork SP, Ho SY et al. Surgical anatomy of tetralogy of Fallot. J Thorac Cardiovasc Surg 1981; 81(6): 887–896.

31. Emmanouilides GC, Thanopoulos B, Siassi B et al. „Agenesis“ of ductus arteriosus associated with the syndrome of tetralogy of Fallot and absent pulmonary valve. Am J Cardiol 1976; 37(3): 403–409.

32. Liao PK, Edwards WD, Julsrud PR et al. Pulmonary blood supply in patients with pulmonary atresia and ventricular septal defect. J Am Coll Cardiol 1985; 6(6): 1343–1350.

33. Anderson RH, Devine WA, del Nido P. The surgical anatomy of tetralogy of Fallot with pulmonary atresia rather than pulmonary stenosis. J Card Surg 1991; 6(1): 41-59.

34. Daubeney PE, Delaney DJ, Anderson RH et al. Pulmonary atresia with intact ventricular septum: range of morphology in a population based study. J Am Coll Cardiol 2002; 39(10): 1670–1679.

35. Brandt PWT, Calder AL, Barratt-Boyes BG, Neutze JM. Double outlet left ventricle. Morphology, Cineangiography, diagnosis and surgical treatment. Am J Cardiol 1976; 38(7): 897-909.

36. Stellin G, Ho SY, Anderson RH, Zuberbuhler JR, Siewers RD. The surgical anatomy of double-outlet right ventricle with concordant atrioventricular connection and non-committed ventricular septal defect. J Thorac Cardiovasc Surg 1991; 102(6): 849-855.

37. Stellin G, Zuberbuhler JR, Anderson RH, Siewers RD. The surgical anatomy of the Taussig-Bing malformation. J Thorac Cardiovasc Surg 1987; 93(4): 560-569.

38. Crupi G, Macartney FJ, Anderson RH. Persistent truncus arteriosus. A study of 66 autopsy cases with special reference to definition and morphogenesis. Am J Cardiol 1977; 40(4): 569-578.

39. Suzuki A, Ho SY, Anderson RH, Deanfield JE. Coronary arterial and sinusal anatomy in hearts with a common arterial trunk. Ann Thorac Surg 1989; 48(6): 792-797.

40. Collett RW, Edwards JE. Persistent truncus arteriosus: a classification according to anatomic types. Surg Clin N Am 1949; 29(4): 1245–1270.

41. Rossi M, Rossi Filho R, Ho SY. Solitary arterial trunk with pulmonary atresia and arteries with supply to the left lung from both an arterial duct and systemic-pulmonary collateral arteries. Int J Cardiol 1988; 20(1): 145-148.

42. Becker AE, Anderson RH. How should we describe hearts in which the aorta is connected to the right ventricle and the pulmonary trunk to the left ventricle? A matter for reason and logic. Am J Cardiol 1983; 51(5): 911-912.

43. Anderson RH, Henry GW, Becker AE. Morphological aspects of complete transposition. Cardiol Young 1991; 1(1): 41-53.

44. Allwork SP, Bentall HH, Becker AE et al. Congenitally corrected transposition of the great arteries: morphologic study of 32 cases. Am J Cardiol 1976; 38(7): 910–923.

45. Anderson RH, Becker AE, Gerlis LM. The pulmonary outflow tract in classically corrected transposition. J Thorac Cardiovasc Surg 1975; 69(5): 747-757.

46. Massoudy P, Baltalarli A, de Leval MR et al. Anatomic variability in coronary arterial distribution with regard to the arterial switch procedure. Circulation 2002; 106(15): 1980-1984.

47. Anderson RK, Lie JT. Pathologic anatomy of Ebstein’s anomaly of the heart revisited. Am J Cardiol 1978; 41(4): 739–745.

48. Ho SY, Anderson RH. Coarctation, tubular hypoplasia and the ductus arteriosus. Histological study of 35 specimens. Br Heart J 1979; 41(3): 268-274.

49. Pellegrino A, Deverall PB, Anderson RH et al. Aortic coarctation in the first three months of life. An anatomopathological study with respect to treatment. J Thorac Cardiovasc Surg 1985; 89(1): 121-127.

50. Ho SY, Wilcox BR, Anderson RH, Lincoln JCR. Interrupted aortic arch--anatomical features of surgical significance. Thorac Cardiovasc Surgeon 1983; 31(4): 199-205.

51. Jacobs JP, Maruszewski B. Functionally univentricular heart and the fontan operation: lessons learned about patterns of practice and outcomes from the congenital heart surgery databases of the European association for cardio-thoracic surgery and the society of thoracic surgeons. World J Pediatr Congenit Heart Surg 2013; 4(4): 349-355.

52. Van Praagh R, Ongley PA, Swan HJC. Anatomic type of single or common ventricle in man. Morphologic and geometric aspects of 60 necropsied cases. Am J Cardiol 1964; 13(3): 367-386.

53. Anderson RH, Becker AE, Tynan M et al. The univentricular atrioventricular connection: getting to the root of a thorny problem. Am J Cardiol 1984; 54(7): 822–828.

54. Keeton BR, Macartney FJ, Hunter S et al. Univentricular heart of right ventricular type with double or common inlet. Circulation 1979; 59(2): 403-411.

55. Anderson RH, Becker AE, Macartney FJ, Shinebourne EA, Wilkinson JL, Tynan MJ. Is “tricuspid atresia” a univentricular heart? Pediatr Cardiol 1979; 1(2): 51-56.

56. Rigby ML, Carvalho JS, Anderson RH et al. The investigation and diagnosis of tricuspid atresia. Int J Cardiol 1990; 27(1): 1–17.

57. Van Son JAM, Edwards WD, Danielson GK. Pathology of coronary arteries, myocardium and great arteries in supravalvular aortic stenosis. Report of five cases with implications for surgical treatment. J Thorac Cardiovasc Surg 1994; 108(1): 21–28.

58. Elzenga NJ, Gittenberger de Groot AC. Coarctation and related aortic arch anomalies in hypoplastic left heart syndrome. Int J Cardiol 1985; 8(4): 379–393.

59. Aiello VD, Ho SY, Anderson RH, Thiene G. Morphologic features of the hypoplastic left heart syndrome-A reappraisal. Pediatr Pathol 1990; 10(6): 931-943.

60. Bull C, de Leval M, Mercanti C, Macartney FJ, Anderson RH. Pulmonary atresia with intact ventricular septum: a revised classification. Circulation 1982; 66(2): 266-271.

61. Stamm C, Anderson RH, Ho YS. Clinical anatomy of the normal pulmonary root compared with that in isolated pulmonary valvular stenosis. J Am Coll Cardiol 1998; 31(6): 1420–1425.

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