|Year : 2005 | Volume
| Issue : 1 | Page : 44-45
Peeping through heart's window: A case report of Fallots tetralogy
R Bhowate, A Dubey
Department of Pedodontics, G.D.C. Raipur, Chattisgarh, India
Department of Pedodontics, G.D.C. Raipur, Chattisgarh
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Tetralogy of Fallot is a congenital heart defect. A combination of four abnormalities in heart allow oxygen rich and oxygen-depleted blood to mix. The resulting low-oxygen blood then circulates through the body. A child with the condition tends to develop slowly, eat poorly and grow slowly and may experience "blue" spells on crying and dyspnea on exertion. A 12 year old child with this congenital heart defect and cleft palate with cleft lip is discussed. Details of the latest diagnostic and treatment procedures are also presented.
Keywords: Cleft Palate, Cyanotic congenital heart disease, Fallots Syndrome, Pulmonary Atresia-Ventricular Septal defect, ToF
|How to cite this article:|
Bhowate R, Dubey A. Peeping through heart's window: A case report of Fallots tetralogy. J Indian Soc Pedod Prev Dent 2005;23:44-5
|How to cite this URL:|
Bhowate R, Dubey A. Peeping through heart's window: A case report of Fallots tetralogy. J Indian Soc Pedod Prev Dent [serial online] 2005 [cited 2021 Mar 1];23:44-5. Available from: https://www.jisppd.com/text.asp?2005/23/1/44/16028
Tetralogy of Fallot (ToF) is the most common form of cyanotic congenital heart disease. It is a combination of four different defects viz. ventricular septal defect (VSD); obstructed out flow of blood from the right ventricle to the lungs (Pulmonary stenosis); a displaced aorta, which causes blood to flow into the aorta from both the right and left ventricles (dextra position or over riding aorta) and right ventricle hypertrophy (RVH). The cause of ToF is unknown. Genotype 22q 11 deletion has been related to faulty development pathway of pulmonary vessels in ToF. Marfan's Syndrome has also been associated with ToF. Intra orally, cyanosis is seen on vermilion border of lips, tongue, buccal mucosa and gingivae. The degree of gingival cyanosis corresponds closely to general degree of cyanosis.- The cyanotic gingiva may be swollen and it is also observed that children with ToF may show periodontal destruction. Insufficient lip seal and geographic tongue are frequently co-existing oral findings.
| Case Report|| |
A 12 years old male child reported for correction of malaligned tooth. Patient gave a history of surgical treatment for congenital heart defect and cleft palate. The child was born out of non-consanguineous marriage, by LSCS for prolonged labour. Patient's mother gave history of viral fever during first trimester. The child was detected to have heart disease on day 1 of life when cyanosis was apparent. Cyanosis worsened every time during cry and on exertion. There was no history of spells or squatting in early childhood. Chest radiograph showed boot shaped heart due to RVH and clear lungs. Hb% level was found to be 25.2 gram % before surgery. 2-D echo cardiographic examination revealed a large paramembranous VSD (0.80 cm), 50% Over riding of aorta, generalized right ventricular hypertrophy, hypoplastic pulmonary artery and dysplastic pulmonary valves. At the age of 8 year, the child was planned for right modified Blalock Taussig shunt (6 mm PTFE Graft). Child recovered well postoperatively. Patient required prolonged pleurocentesis (right side). Prior to surgical treatment of the cardiac defect, cleft palate had been repaired previously in 5 stages.
Clinical examination revealed clubbing and flat foot. Intra oral examination revealed operated cleft lip and closure in palatal cleft region [Figure - 1]. Crowding and "v" shaped anterior maxillary arch was present .The maxillary arch was under developed transversely and 12,15],25 were congenitally missing. 55,16,65,26,36,46 were found to be decayed [Figure - 2]. Relative macroglossia due to under developed maxillae and cleft palate was present.
Decayed permanent teeth were restored and the child was referred to orthodontist, wherein treatment was planned into 4 distinct but inter related stages:
PHASE I: Expansion of maxillary arch and protrusion of maxillary arch.
PHASE II: Bone grafting in opened up space for arch stabilization.
PHASE III: Arch alignment with orthodontic mechanotherapy and setting of occlusion.
PHASE IV: Cosmetic plastic surgery for lip and palate.
| Discussion|| |
Cardio vascular diseases are common and it is inevitable that any practitioner dealing with patients will encounter it. This underlines the need for correct diagnosis from clinical picture and laboratory findings. Blood studies show polycythemia and high hematocrit. X-ray chest reveals oligemic lung fields (poorly vascularized lungs), a small boot shaped heart with the tip of boot turned up and above diaphragm (because of right ventricular hypertrophy) and concavity of pulmonary artery. ECG demonstrates right axis deviation, an evidence of right ventricular hypertrophy with beaked P-waves. 2-D echocardiographs establishes the diagnosis and provides information as to the extent of aortic over ride on the septum, location and degree of right out flow tract obstruction, size of proximal branch pulmonary artery and the side of aorotic arch. Cardiac catheterization demonstrates a systemic pressure. The number of sub epithelial gingival vessels per square millimeter in patient with ToF is significantly higher than in healthy subjects. After thoracic surgery, the number of gingival blood vessels drops back to normal.
Unless the child's heart is repaired surgically ToF is fatal. Cyanotic spells usually respond to oxygen, morphine and knee-to-chest position. Prostaglandin E is found to be of same use to improve blood flow through lungs. Propanolol is given to prevent hypoxic spells. Open-heart surgery is done to close the defect in the septum, remove extra heart muscle and open/repair the pulmonary valve at early age (less than 1 year)., While performing dental procedures, sevoflurane is found to be better alternative than Halothane as an induction agent.
It is stressed that dental treatment plan for patients with ToF must take into account the patients medical status prior to and following corrective surgical procedures Preoperative evaluation of cardiac function is must, lest patient might show Arrythmias. These patient are also susceptible to SABE following minor surgery and dental extractions, hence patient should be put on antibiotic prophylaxis before any surgery or dental work. Pulpectomy is questionable in these patients as ToF patients might suffer from cerebral abscess due to inadequate cleaning of lateral and accessory canals.
| References|| |
|1.||Hazare VK, Chaoji KH, Daftary DK. Pallets Tetralogy Dental Dialogue 1986;1and2:19-22. |
|2.||Cheesa M, Buttera G, Bahoeffer P, et al. Relation of genotype 22ql 1 deletion to phenotype of pulmonary vessels in tetralogy of Pallet and pulmonary atresia-ventricular septal defect. Pediatr Cardiol 1998;19:289-96. |
|3.||Pannu HS, Avasthi GL, Sood NK. Tetralogy of Pallets co-existing with marfans syndrome an uncommon association. Indian J Opthalmol 1992;40:61-2. |
|4.||Frosslund C. The occurrence of sub epithelial gingival blood vessels in patients with morbus caerleus (tetralogy of Pallet). Acto Odont Scand 1962;20:301-6. |
|5.||Gould MSE, Picton DC. A The gingival condition of congenital cyanotic individuals. Brit Dent J 1968;109:96-100. |
|6.||Daftary DK, Hazare VK. An oral mucosa. It's clinical significance in child. Jour Ind Dent Assoc 1980;51:381-5. |
|7.||Green WM, Meechan JG. General medicine and Surgery or Dental practitioners. Part 1: Cardiovascular system. BDJ 2003;194:537-42. |
|8.||Spivack E. Tetralogy of Fallot: An overview, case report and discussion of dental implications. Spec Care Entist 2001;21:172-5. [PUBMED] |
|9.||Helbing WA, Roest AA, Niezen RA, et al. ECG precditors of ventricular arrythmias and biventricular size and wall mass in tetralogy of Fallot with pulmonary regurgitation. Heart 2002;88:515-9. [PUBMED] [FULLTEXT]|
|10.||Andrew S, Mackie MD. Echo Cardiographic Predictors of aorto pulmonary Collaterals in infants with tetralogy of Fallot and pulmonary Atresia. J Am Coll Cardiol 2003;41:852-7. |
|11.||Lewis AB, Lurie PR. Prolonged Prostaglandin E, infusion in an infant with cyanotic congenital heart disease. Pediatrics 1978;61:534-6. [PUBMED] |
|12.||Barazzone C, Jaccard C, Benner M, et al. Propanalol treatment in children with tetralogy of Fallot alters the response to Isoprenaline after Surgical Repair. Br Heart J 1988;60:156-61. |
|13.||Chiu CL, Wang CY. Sevoflurane for dental extraction in children with tetralogy of Fallot. Pediatr Anaesth 2000;10:227-9. |
|14.||Imai FH, Satoh KA. Arrythmias during extraction of the 3rd molars using IV sedation. A case of post operative tetralogy of Fallot. Fukuoka Shika Daigaku Gakkai Zaashi 1989;16:495-500. |
|15.||Pandian JD, Moosa NV, Cherian PJ, Radhakrishnan K. Brainstem abscess complicating tetralogy of Fallot successfully treated with antibiotcs alone. Neurol India 2000;48:272-5. [PUBMED] [FULLTEXT]|
[Figure - 1], [Figure - 2]