Congenital diaphragmatic hernia is the outcome of the abdominal contents in the thorax by a breach caused by a failure of the closure of the pleuroperitoneal canal. It is a rare disease  and severe affecting 1/3500 births with a mortality between 30% and 60%. Management in a referral center improves the survival of patients  . It usually left sided  . The symptomatology varies according to the site and the size of the diaphragmatic breach. We report here a case of congenital diaphragmatic hernia successfully managed.
2. Case Description
It was a newborn baby, referred at the fifth hour of life for a very severe respiratory distress with a SILVERMAN scale rated at 7/10. The gestational history noted a well-attended pregnancy with 7 antenatal consultations, serology (toxoplasmosis, rubella, syphilis, HIV) were negative and the three ultrasounds were normal. The 22-year-old mother, a primigravida, had delivered by Caesarean section at the end of 38SA + 6 days for acute foetal suffering with extraction by the cephalic pole of a male newborn baby crying immediately. The APGAR score was 8 in the first minute, 9 in the fifth and 10 in the tenth minute. Neonatal measurements were normal. The amniotic fluid was meconium-strained. The infant had secondarily presented a severe respiratory distress. The initial examination in our center revealed an average general impression, a respiratory distress with respiratory rate at 88 cycles per minute and signs of respiratory struggle, tachycardia at 160 beats per minute, 88% oxygen saturation at ambient air. The thorax was discreetly asymmetric with an abolition of vesicular murmur in the left lung field and a flat, soft abdomen. The thoraco-abdominal radiography revealed a clear left intra-thoracic image with erasure of the left diaphragmatic dome; mass effect on the left pulmonary parenchyma rolled upwards and on the mediastinum organs deviated to the right (Figure 1). The diagnosis of left diaphragmatic hernia was posed indicating a surgical cure. Hospitalized in neonatology unit, under oxygen therapy at 5 L/min by an endotracheal tube in right lateral decubitus, the respiratory state remained stable. At the abdominal laparotomy on the 5th day of life, part of the abdominal viscera (stomach, spleen, left lobe of the liver, left half of the left transverse colon, left part proximal part of the descending colon) leaving the thorax by a left diaphragmatic breach measuring 5 cm by 4 cm (Figure 2). There were no other visceral abnormalities. A reduction of the hernia had been made, which made it possible to recover a hernial sac consisting of the pleura and the parietal peritoneum; then a closure of the breach by separate points at Mersuture 2.0 on a thoracic drain with anti-reflux system (Figure 3). The operation had few after-effects with a complete regression of the respiratory distress. The thoraco-abdominal X-ray, performed on the third day after surgery, noticed a good left lung expansion with the clearance of the mass effect on the mediastinum; the right pulmonary parenchyma was healthy (Figure 1). Clinical examination was normal after five months follow-up with a very good cardio-pulmonary function. Sociodemographic characteristic and signs of the patient were resumed in Table 1.
Its frequency is 1 case for 2000 to 5000 live births  . It accounts for 8% of all major congenital anomalies  . In 90% of cases the diaphragmatic defect is posterolateral and in 80% of cases it is on the left [2 = D3]. The sex ratio is 2  . In our case, the subject was male and the defect was postero left lateral.
Figure 1. Thoraco-abdominal X-ray of face. (a) Pre-operative thoraco-abdominal X-ray showing intra thoracic clarity and heart and big vessels deviated on the right; (b) Post-operative thoraco-abdominal X-ray performed on the third day after surgery showing good left lung expansion. With clearance of the mass effect on the mediastinum. Right pulmonary parenchyma was healthy.
Figure 2. Per operative picture showing a left diaphragmatic breach.
Its etiology is still unknown in most cases. There is a family association in 2% of cases. In 15% of cases, there are chromosomal abnormalities. Recently, it was discovered that the 15q26 region is involved in the development of the diaphragm  . Trisomies 13, 18 and 21 are the genetic associations most often found. 40% of congenital diaphragmatic hernias are associated with major malformations (cardiac, musculoskeletal, neurological, genitourinary)  . In our case, there was no major malformation associated with it.
Pulmonary hypoplasia begins in embryonic period even before the formation of the diaphragm. It is aggravated by the presence of the abdominal organs in the thorax. The anomalies also concern the upper airways which are under developed,
Figure 3. Per operative picture showing the diaphragmatic breach repaired.
Table 1. Sociodemographic characteristics and signs.
the intra-pulmonary arteries which are reduced per unit of pulmonary volume and whose walls are thickened.
Antenatal diagnosis of congenital diaphragmatic hernia is possible from the second quarter of pregnancy, and is based on the presence of the stomach or intestines in the thorax. This diagnosis can be difficult in the absence of an intra-thoracic stomach or when the diaphragmatic defect is on the right side  . In our case, 3 ultrasounds were performed which did not reveal abnormalities. The research of associated malformations in antenatal, especially cardiac and musculoskeletal is useful to assess the prognosis. In the search for chromosomal abnormality, amniocentesis is useful.
After birth, the clinical signs are variable according to the size and site of the diaphragmatic breach; but also of the volume of herniated abdominal organs. When there is a large breach, the symptomatology is noisy with a respiratory distress syndrome made of dyspnea, cyanosis and tachycardia, present from birth. This respiratory distress is at the origin of a distension of the intra-thoracic digestive loops; which exerts additional pressure on the hypoplastic lung. When the breach is small, the symptomatology may be mute for several months, and the diagnosis of diaphragmatic hernia is fortuitous in the context of the exploration of digestive or respiratory manifestations. When the breach is located on the right side, the diagnosis is often difficult because of the presence of the liver which prevents the penetration of the abdominal contents into the thorax  . In our case, this was a large breach on the left side with a large part of the abdominal contents in the thorax. The clinical picture was that of early respiratory distress.
On the para-clinical level, chest X-ray or better with a naso-gastric tube can be used to diagnose  . This diagnosis can be confirmed by oeso-gastro-duodenal transit, which shows an opacification of the stomach in the thorax, but this examination fails to underestimate the degree of hernia  . Scanning and scintigraphy of the liver and spleen are useful for diagnosis in right diaphragmatic hernias  .
In preoperative management, respiratory assistance is provided by intubation and ventilation with low inspiratory pressure (less than 25 cm of water) to minimize lung damage and maintain oxygen saturation above 85%. Oxygenation by bezel or mask is contraindicated due to the gastric distension it generates. The installation of a naso-gastric tube with a gentle aspiration is useful to ensure decompression of the digestive tract  . Extracorporeal membrane oxygenation is used in cases of severe hypoxia and stabilization of newborn babies before and during surgery  . Nitric oxide is a selective pulmonary vasodilator used to improve oxygenation in patients with pulmonary hypertension  . Surgical management now delayed 24 to 48 hours to ensure clinical stabilization and a fall of the pulmonary hypertension; consists of a closing of the diaphragmatic breach by suture or by a prosthesis  .
Patient care was provided by the placement of a naso-gastric tube and oxygenation by endotracheal tube in right lateral decubitus which allowed the respiratory state to be maintained until surgery. The surgical cure was performed by laparotomy on the 5th day of life with drainage of the diaphragmatic space.
A laparoscopic surgical cure has been described in the literature for late-onset cases in stable patients  .
The development of the operated diaphragmatic hernia is enamelled by complications. There are respiratory complications (bronchopulmonary dysplasia, pulmonary arterial hypertension, bronchospasms, and recurrent respiratory infections); digestive complications (gastroesophageal reflux); neurological complications; musculoskeletal complications (scoliosis, pectus excavatus or carinatus); a growth retardation   .
Mortality is 48% in isolated forms; association with a malformation or prematurity aggravates the prognosis with a mortality of 80% and 83% respectively  . This last decade, our teaching hospital had registered five cases of congenital diaphragmatic hernia which all had been operated with a mortality of 20%. This good falsely mortality rate could be explained by the smallness of our number.
Thanks to advances in prenatal diagnosis and early multidisciplinary care, survival is 80%  .
This clinical fact questions us because of the severity and the rarity of congenital diaphragmatic hernia in Benin. It points out the benefit of the possibility of antenatal diagnosis using classic obstetric ultrasounds. Its treatment is surgical by an abdominal approach. Its prognosis depends on the cardiac and pulmonary malformations which may be associated with it and which must be systematically investigated.
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