Spontaneous Pneumomediastinumin Term Neonate: A Case Report

Case Report

Austin J Clin Case Rep. 2020; 7(2): 1167.

Spontaneous Pneumomediastinumin Term Neonate: A Case Report

Wegdan Helmy Mawlana1 and Asmaa Osman2

1Department of Pediatrics and Neonatology, Tanta University Hospital, Egypt

2Divison of Neonatology, Department of Pediatrics, King Salman Armed Forces Hospital, Saudi Arabia

*Corresponding author: Wegdan Helmy Mawlana, Department of Pediatrics and Neonatology, Tanta University Hospital, Egypt

Received: July 28, 2020; Accepted: August 21, 2020; Published: August 28, 2020

Abstract

Pneumomediastinum is an uncommon cause of respiratory distress in term infants. It could be due to many risk factors; vigorous resuscitation, pneumonia, mechanical ventilation or meconium aspiration syndrome. We present a case of spontaneous pneumomediastinum in a term baby with no identified risk factor.

Keywords: Newborn; Pneumomediastinum; Air leak

Introduction

Pneumomediastinum is uncommon cause of respiratory distress in term infants. The actual incidence is unknown since most of those infants are asymptomatic [1]. Term infants with meconium aspiration syndrome, pneumonia, vigorous resuscitation at birth, lung hypoplasia and ventilator support are at high risk [2]. We report a clinical case of term infant with significant pneumomediastinum without identifiable risk factors.

Case Presentation

A Term baby boy with gestational age 38+6 weeks was born by spontaneous vaginal delivery to 28 years old G2P1 Saudi female. His birth weight was 2.5 kg with APGAR score 8 and 9 at 1 and 5 minutes respectively. He did not require any resuscitation. Shortly after birth he developed grunting with mild respiratory distress, so he was kept in the nursery under observation with oxygen supply by nasal cannula for 2 hours but with no improvement so he was admitted to our NICU for further investigations.

On admission baby looks well, active, not dysmorphic, vitally stable, chest examination showed grunting with fair air entry bilaterally. Other systemic exam unremarkable. CXR done at 3 hours of life showed significant pneumo mediastinum with spinnaker-sail sign (Figure 1). Capillary blood gas was normal (ph 7.33, Pco2 40, Hco3 18, BE -3.) SO2 was ≥95% on nasal cannula oxygen saturation was 21 to 25%. His respiratory distress improved dramatically with weaning from nasal cannula oxygen by day 2 of life. Because of significant pneumomediastinum as shown in the first x-ray, he was kept under close observation and follow up with serial x-rays till day 9 of life (Figure 2). It showed persistent same radiologic finding with no regression (Figure 3). For that, CT chest was done that confirmed the same finding with no other abnormalities. On admission white cell blood count was normal and blood culture was sterile. Baby was discharged home on day 10 of life with follow up after 2 wks. X-ray done then showed resolved pneumomediastinum.

Figure 1: Plain radiograph of the chest, showing the Spinnaker-Sail Sign. Both lobes of the thymus are lifted and displaced into the upper mediastinum, creating a wedge-shaped opacity. This resembles a Spinnaker sail.

    

    
    

    

    Figure 1: Plain radiograph of the chest, showing the Spinnaker-Sail Sign.
Both lobes of the thymus are lifted and displaced into the upper mediastinum,
creating a wedge-shaped opacity. This resembles a Spinnaker sail.

Figure 2: Plain radiograph of the chest, showing the Spinnaker-Sail Sign.

    

    
    

    

    Figure 2: Plain radiograph of the chest, showing the Spinnaker-Sail Sign.

Figure 3: Plain radiograph of the chest, showing the Spinnaker-Sail Sign.

    

    
    

    

    Figure 3: Plain radiograph of the chest, showing the Spinnaker-Sail Sign.

Discussion

A pneumomediastinum is air dissecting into the hilum through the perivascular sheaths from ruptured alveolar air into the mediastinum [3]. It has been estimated to occur spontaneously in 25 of 10,000 live births in asymptomatic infants [4]. Apparent risk factors included vigorous resuscitation, mechanical ventilation, meconium aspiration syndrome and prematurity [5]. Interestingly, our case has no identifiable risk factors. Our baby boy was born at term by spontaneous vaginal delivery, did not receive any resuscitation, and only required nasal cannula oxygen for few hours. This could be explained by the pressure gradient between the alveolar and perivascular space that could be abnormally high during crying of the baby and an alveolar rupture may occur [6]. Chest x-ray is usually enough to diagnosis pneumomediastinum, it may show a halo around the heart border or air elevating the thymus and giving rise to a crescentic configuration and a wind blown spinnaker sail as in our patient [7,8].

Conservative management and close observation is the standard of care in almost all cases as the majority of them show spontaneous resolution [9]. However some cases may be presented with severe respiratory distress that requires high frequency ventilation [10]. Few reported cases required drainage [11]. Luckily our baby was in room air with no signs of distress on the second day .Because of the potential risk of deterioration of the clinical status; pneumo thorax, subcutaneous, and interstitial emphysema he was kept under observation with repeated chest x-rays that showed persistent pneumo mediastinum till day nine of life, so CT chest was done to exclude any other anomalies. Chest CT confirmed the same finding. Baby was discharged home on day ten of life. He was examined after 2 weeks, he was doing well and chest x-ray showed resolved penumomediastinum.

Conclusion

Pneumediastinum can occur in term infants with no identified risk factors. Most of them resolve spontaneously.

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Citation: Mawlana WH and Osman A. Spontaneous Pneumomediastinumin Term Neonate: A Case Report. Austin J Clin Case Rep. 2020; 7(2): 1167.