Case Reports in Pediatrics
Volume 2015 (2015), Article ID 128409, 3 pages
http://dx.doi.org/10.1155/2015/128409

Case Report

Nephrotic Syndrome in a Child Suffering from Tetralogy of Fallot: A Rare Association

Pépé Mfutu Ekulu,¹ Orly Kazadi-wa-Kazadi,¹ Paul Kabuyi Lumbala,² and Michel Ntetani Aloni¹

¹Division of Paediatric Haemato-Oncology and Nephrology, Department of Paediatrics, University Hospital of Kinshasa, Faculty of Medicine, University of Kinshasa, Kinshasa, Congo
²Division of Cardiology, Department of Paediatrics, University Hospital of Kinshasa, Faculty of Medicine, University of Kinshasa, Kinshasa, Congo

Received 8 May 2015; Revised 8 July 2015; Accepted 21 July 2015

Academic Editor: Larry A. Rhodes

Copyright © 2015 Pépé Mfutu Ekulu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Nephrotic syndrome is an uncommon complication of tetralogy of Fallot and has been rarely reported in pediatric population. We describe a 4-year-old female Congolese child who was referred for investigation for persistent dyspnea, edema, and cyanosis and nephrotic range proteinuria. Our patient presented with a tetralogy of Fallot and nephrotic syndrome. Conclusion. This case reminds us that children with tetralogy of Fallot may develop nephrotic proteinuria.

1. Introduction

Glomerular dysfunction can be found in cyanotic congenital heart disease (CHD) especially in older children and adults, being associated occasionally with proteinuria and microalbuminuria [1, 2]. The risk of developing renal impairment is particularly high in cyanotic patients particularly in patients with long-standing cyanotic CHD [1, 2]. However, nephrotic syndrome (NS) is an uncommon complication of cyanotic congenital heart disease and is rarely reported. This complication has not been documented in Congolese children.

2. Case Report

A 4-year-old girl with edema, dyspnea, and cyanosis was referred from Butembo at the East of the Democratic Republic of Congo (DRC) to a facility renal and cardiology investigations in Department of Pediatrics of University Hospital of Kinshasa, Kinshasa, DRC. The history of present illness dates back to about 13 months characterized by progressive cough, dyspnea, and orthopnea. Physical examination revealed respiratory distress with edema and episodes of squatting. She was cyanosed with finger and toes clubbing. Apex beat was at the fifth intercostal space anterior axillary line. Both heart sounds were noted with a systolic thrill and loud systolic ejection murmur grade 3. The blood pressure was 150/110 mmHg, and oximetry was 63%.

A complete blood count showed hemoglobin 23.2 g/dL, total proteins 45 g/L, and albumin 22 g/L. Dipstick urinalysis was 3 + while the 24-hour urinary protein was 154 mg/kg. Creatinine was 37 μmol/L, urea was 3.8 mmol/L, cholesterol was 4.3 mmol/L, and HDL was 1.3 mmol/L. HIV and hepatitis serology were negative. Anti-streptolysin O (ASLO) was <200 IU.

X-ray revealed “boot shaped" heart with an upturned cardiac apex (Figure 1). Echocardiography revealed tetralogy of Fallot with hypoplastic pulmonary artery and biventricular dysfunction. Cardiac catheterization was not performed due to technical reasons. A diagnosis of Fallot’s tetralogy and NS was established. Renal biopsy was contraindicated because of the deteriorating renal condition and cardiac status.

Figure 1: Plain film shows a “boot shaped” heart with an upturned cardiac apex due to right ventricular hypertrophy and concave pulmonary arterial segment.

During her hospitalization, the child received specific treatment for her blood hypertension, associated furosemide (1 mg/kg/dose, every six hours), Propranolol (2 mg/kg, every six hours), and Enalapril (0.4 mg/Kg, every twelve hours). For her NS, the child received prednisone (60 mg/m²/day during 30 days) for the first phase and diet.

Initial biologic and clinical improvement was observed with steroid and Enalapril therapies. Edema regressed with treatment. The 24-hour urinary protein decreased from 154 mg/kg to 6.7 mg/kg and creatinine remained stable. Death occurred 41 days after admission to an array of sudden hypoxic tet spells. She was stable enough to be discharged after six weeks on admission.

3. Discussion

Nephropathy among patients is an important complication of tetralogy of Fallot [1, 2]. The incidence and prevalence are unknown and epidemiological data are rare in Africa. In Central Africa, this affection was not previously noted. Our observation is the first description in our population. Only three cases in pediatric population could be found in Nigeria with the use of available computer-assisted medical literature search programs [1, 2]. The situation is probably due to the lack of the evaluation of renal function in highly resource-scarce settings and nephrologist pediatrician [3]. At the same time, it is probable that many children with cyanotic CHD die before the development of NS in our midst.

We have reviewed the literature on cyanotic CHD and NS (Table 1). The development of NS associated with cyanotic CHD remains unclear. However, some aetiopathogenetic mechanisms have been suggested for the development of nephropathy. The patients with cyanotic CHD are exposed to chronic hypoxia. The risk of developing glomerular lesions rose sharply during the second decade of life if the cyanosis remains unchanged for more than ten years [4, 5]. Hyperviscosity due to polycythemia may induce an angiogenic increase in the glomerular capillary beds, in turn leading to glomerulomegaly. Glomerulomegaly is a consequence of the hyperperfusion of glomeruli associated with the chronic hypoxia and the increased hydrostatic pressure in the capillary wall. This situation is a causative factor of the deterioration and the decline of renal function, in the condition of polycythemia. Furthermore, the failure of a compensatory mechanism to respond to reduced RPF by hyperfiltration may be accompanied by the development and progression of microalbuminuria and proteinuria [4–6]. The pathogenesis and development of nephrotic proteinuria range are the result of these combined mechanisms. Although we could not perform the renal biopsy, the nephrotic range proteinuria is probably a consequence of focal and segmental glomerulosclerosis.

Table 1: Results of the literature review of cyanotic CHD associated with nephrotic syndrome in African children.

Source
Our case
Adedoyin and Afolabi [2]
Ogunkunle et al. [1]
Ogunkunle et al. [1]

Country
Kinshasa, DRC
Ilorin, Nigeria
Ibadan, Nigeria
Ibadan, Nigeria

Year of description
2015
2006
2008
2008

Age (years)
4
9
12
7

Gender
Female
Male
Female
Male

Cyanotic CHD
Tetralogy of Fallot
Truncus arteriosus
Tetralogy of Fallot
Tricuspid atresia

CHD: congenital heart disease; DRC: Democratic Republic of Congo.

Our patient presented late. This case revealed the problem of early diagnosis, regular follow-up, and early detection of complications in African cyanotic CHD patients especially in case of Fallot’s tetralogy during antenatal or neonatal period. It is known that untreated cardiac malformations in patient with Fallot’s tetralogy have high likelihood of progression to glomerular damage [4–6]. In our context, diagnosis and management were generally delayed.

It is worth considering the use of ACE-I when nephropathy accompanies cyanotic CHD. In a previous study, Enalapril apparently reduced the urinary protein excretion in 80% of patients [7]. In our case, proteinuria decreased from 154 mg/kg/24 h to 6.7 mg/kg/24 h.

This case reminds us that children with tetralogy of Fallot may develop NS. This case report is pointing out the problem encountered in the early diagnosis and management of cyanotic CHD in resource-limited settings as in DRC. Considering the paucity of facilities available for medical and surgical management of Fallot’s tetralogy in our midst, we recommend early detection of this congenital heart disease and regular renal screening of patients and thus allow, at least at this stage, the initiation of ACE-I. However, it has to be stated that, in countries such as the DRC, early corrective cardiac surgery should be the first choice particularly in patients who otherwise present severe complications of their cyanotic CHD and reduce the risk of the development of chronic renal failure.

Ethical Approval

This study was determined to be Non-Human/Non-Research by the Ethical Committee of the Public Health School of the University of Kinshasa, Kinshasa, DRC.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

O. O. Ogunkunle, A. O. Asinobi, S. I. Omokhodion, and A. D. Ademola, “Nephrotic syndrome complicating cyanotic congenital heart disease: a report of two cases,” West African Journal of Medicine, vol. 27, no. 4, pp. 263–266, 2008.

O. T. Adedoyin and J. K. Afolabi, “Sudden deterioration in the renal function of an African child with cyanotic congenital heart disease,” Journal of the National Medical Association, vol. 98, no. 2, pp. 287–289, 2006.

P. Cochat, C. Mourani, J. Exantus et al., “Pediatric nephrology in developing countries,” Medecine Tropicale, vol. 69, no. 6, pp. 543–547, 2009.

S. Dittrich, N. A. Haas, C. Bührer, C. Müller, I. Dähnert, and P. E. Lange, “Renal impairment in patients with long-standing cyanotic congenital heart disease,” Acta Paediatrica, vol. 87, no. 9, pp. 949–954, 1998.

F. Krull, J. H. H. Ehrich, U. Wurster, U. Toel, S. Rothgänger, and I. Luhmer, “Renal involvement in patients with congenital cyanotic heart disease,” Acta Paediatrica Scandinavica, vol. 80, no. 12, pp. 1214–1219, 1991.

J. Inatomi, K. Matsuoka, R. Fujimaru, A. Nakagawa, and K. Iijima, “Mechanisms of development and progression of cyanotic nephropathy,” Pediatric Nephrology, vol. 21, no. 10, pp. 1440–1445, 2006.

Y. Fujimoto, M. Matsushima, K. Tsuzuki et al., “Nephropathy of cyanotic congenital heart disease: clinical characteristics and effectiveness of an angiotensin-converting enzyme inhibitor,” Clinical Nephrology, vol. 58, no. 2, pp. 95–102, 2002.