2008, Number 3
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Arch Cardiol Mex 2008; 78 (3)
Anomalous pulmonary venous connection
Muñoz CL, Kuri NM, Sánchez VCA, Espínola ZN
Language: Spanish
References: 29
Page: 247-254
PDF size: 179.54 Kb.
ABSTRACT
An anatomical-embryological correlation of anomalous venous pulmonary connection is presented to gain an insight of its pathogenesis. The basic publications on embryonic development of the pulmonary veins were analyzed in its two stages: the primary connection of these veins (collectors) with the embryonic systemic veins from which the definitive veins arise. These channels normally disappear once the pulmonary veins sinus is connected with the roof of the left atrium (secondary definitive connection); when the latter does not exist, any of the primitive channels persist and originates the anatomic sites of the anomalous venous pulmonary connection. The embryonic systemic veins are the right cardinal (superior vena cava and azygos vein), the left cardinal (venous coronary sinus and vertical vein) and the umbilical-vitelline (portal vein and ductus venosus). Other mechanisms are discussed such as ectopic origin of the primitive pulmonary vein in the roof of the right atrium and misplaced left of the atrial septum. The atrial septal defect is conditioned by the hemodynamics of this malformation. The knowledge of the pulmonary venous development is of great value in understanding the structure and the anatomic variants of this cardiovascular malformation in its total and partial forms.
REFERENCES
Auer J: The development of the human pulmonary vein and its major variations. Anat Rec 1948; 101: 581-595.
Neill CA: Development of the pulmonary vein with reference to the embryology of anomalies of pulmonary venous return. Pediatrics 1956; 18: 880-887.
Muñoz Castellanos L, García C, Zawilski J, Corona E, Espino Vela J: Desembocadura anómala de las venas pulmonares. Arch Inst Cardiol Mex 1968; 38: 897-918.
Edwards JE, Helmholz HF Jr: A classification of total anomalous pulmonary venous connection based on developmental considerations. Mayo Clin Proc 1956; 31: 151-160.
Edwards JE: Pathologic and developmental considerations in anomalous pulmonary venous connection. Mayo Clin Proc 1953; 28: 441-452.
Garson A, Bricker T: The science and practice of pediatric cardiology. Vol. 2 Philadelphia. Lea & Febiger, 1990, pp 1145-1174.
Van Praagh R, Corsini I: Cor triatriatum: Pathologic anatomy and a consideration of morphogenesis based on 13 post mortem cases and a study of normal development of the pulmonary vein and atrial septum in 83 human embryos. Am Heart J 1969; 78: 379-405.
Streeter GL: Developmental horizons in human embryos: Description of age group XII 21 to 29 somites. Contrib Embryol 1942; 30: 231-241.
Streeter GL: Development horizons in human embryos. Description of age group XIII, embryos about 4 or 5 millimeters long. Contrib Embryol 1945; 31: 27-40.
Streeter GL: Developmental horizons in human embryos. Description of age group XV, XVI, XVII and XVIII, being the third issue of a survey of the Carnegie collection. Contrib Embryol 1948; 33: 135-203.
Brody H: Drainage of the pulmonary veins into the right side of the heart. Arch Path 1942; 33: 221-240.
Wilson AD: Total anomalous pulmonary venous connection. Med J 2002; 3: 1-12.
Darling RC, Rotney WB, Craig JM: Total pulmonary venous drainage into the right side of the heart. Report of 17 autopsied cases not associated with other major cardiovascular anomalies. Lab Invest 1957; 6: 44-64.
Becker AE, Anderson RH: Pathology of congenital heart disease. London. Butterworths, 1981, pp 53-61.
Cayre RO, Civetta JD, Roldan AO, Rousseau JJ, Knudson OA-Jr, Valdes Cruz IM: Mixed total anomalous pulmonary venous connection: case report with bilateral venous collectors. J Am Soc Echocardiogr 2003; 16: 84-87.
Watanabe T, Murashita T, Oka J, Hatta E, Imamura M, Yasuda K: Mixed type of total anomalous pulmonary venous return: A rare pattern of pulmonary venous drainage. Kyobu Gek 2001; 54: 1041-1044.
Neill CA, Ferencz C, Sabiston DC, Sheldon H: The familial occurrence of hypoplastic lung with systemic arterial supply and anomalous venous drainage “Scimitar syndrome”. Johns Hopkins Med 1977; 107: 1-10.
Espínola-Zavaleta N, Muñoz-Castellanos L, Játiva-Chávez S, Zamora González C: Correlación anatomo-ecocardiográfica del síndrome de cimitarra en el adulto y comentario embriológico. Arch Cardiol Mex 2005; 75: 165-169.
Hudson REB: The normal and abnormal inter-atrial septum. Br Heart J 1955; 17: 489-495.
Hudson REB: Sinus venosus (superior caval) atrial septal defect. In Cardivascular pathology. London. Edwards Arnold, 1965, pp 1784-1788.
Muñoz Castellanos L, Kuri Nivón M, Espínola Zavaleta N, Salinas Sánchez HC: Defecto septal atrial. Estudio morfopatológico y embriológico. Arch Cardiol Mex 2006; 76: 355-365.
Al-Fadley F, Galal O, Wilson N, Aloufi S: Cor triatriatum associated with total anomalous pulmonary venous drainage in the setting of mitral atresia and restrictive interatrial communication. Pediatr Cardiol 1992; 13: 125-126.
Webber SA, Hatchwell E, Barber JCK, Daubeney PEF, Crolla JA, Salmon SP, et al: Importance of microdeletions of chromosomal region 22q11 in the etiology of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study. J Pediatr 1996; 129: 26-32.
Paz JE, Castilla EE: Familial total anomalous pulmonary venous return. J Med Genet 1971; 8: 312-320.
Nora J: Multifactorial inheritance hypothesis for the etiology of congenital heart disease. Circulation 1968; 38: 604-610.
Redington AN, Raine J, Shinebourne EA, Rigby ML: Tetralogy of Fallot with anomalous pulmonary venous connection: A rare but clinically important association. Br Heart J 1990; 64: 325-328.
Larsen WJ: Embriología humana. Madrid, Elsevier. 2003, pp 229-230.
Carlson B: Embriología humana y Biología del desarrollo. Madrid. Elsevier, 2005, pp 434-436.
Gilbert SF: Biología del desarrollo. Buenos Aires. Panamericana, 2005, pp 535-554.