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International Journal of Pediatrics & Neonatal Care Volume 2 (2016), Article ID 1:IJPNC-114, 2 pages
https://doi.org/10.15344/2455-2364/2016/114
Case Report
Congenital Hemothorax in a Preterm Neonate

Asad Rahman

College of Medicine and Health Sciences, Sultan Qaboos University, Al Khoudh,Muscat 123, Oman
Dr. Asad Rahman, College of Medicine and Health Sciences, Sultan Qaboos University, Al Khoudh,Muscat 123, Oman; E-mail: asad99khan@yahoo.com
01 February 2016; 12 May 2016; 14 May 2016
Rahman A (2016) Congenital Hemothorax in a Preterm Neonate. Int J Pediatr Neonat Care 2: 114. doi: https://doi.org/10.15344/2455-2364/2016/114

Abstract

Congenital idiopathic pleural effusion is a very rare condition in neonates. Majority of the congenital pleural effusion are associated with documented cause such as hydrops fetalis, chromosomal causes, cardiac or pulmonary causes. The congenital effusion is mostly transudate, exudates or chylous. Hemorrhagic pleural effusion without any documented coagulation abnormality is rare. We are reporting a case of unilateral hemorrhagic pleural effusion in a preterm neonate.


1. Introduction

There is very limited data available about congenital neonatal pleural effusion. Two studies have reported the incidence of neonatal pleural effusion between 0.06-2.2 percent [1,2]. The incidence of isolated congenital pleural effusion is about 1 in 12,000 to 1 in 15,000 deliveries [3]. Multiple causes have been associated with congenital pleural effusion. Majority of these disorders present with hydrops fetalis and bilateral pleural effusion. The content of pleural effusion is transudate, exudates or chylous. Hemorrhagic pleural effusion or hemothorax may be associated with DIC or coagulation disorder. We are reporting a preterm neonate with congenital neonatal unilateral hemothorax.

2. Case Report

A pretern newborn was delivered at 33 weeks of gestation by spontaneous vaginal delivery. The mother was 25 year old and was under regular antenatal follow up in our hospital. Antenatal screening was unremarkable. No abnormality was detected in antenatal ultrasound at 20 weeks of gestation. The baby was in severe respiratory distress at birth and needed intubation and positive pressure ventilation. Chest radiograph showed generalized opacity on left side and there was mediastinal shift. Ultrasound showed left sided pleural effusion and a collapsed left lung. The pleural effusion was drained with a chest tube. The analysis of pleural fluid showed hemorrhagic fluid with few lymphocytes and no atypical cells. No microorganism was seen on gram stain and there was no growth on culture. Repeat chest radiograph showed expanded lungs. There was no recollection of pleural effusion and chest tube was removed after 3 days. Hematology and pulmonalogy team was consulted and all work up for pleural effusion was within normal range. Karyotype and chromosomal analysis was normal. Baby was discharged home and being followed up in outpatient clinic.

figure 1
Figure 1: Chest radiograph before chest tube insertion.
figure 2
Figure 2: Repeat chest radiograph after chest tube insertion showing fully expanded lung without any residual pleural effusion.

3. Discussion

Congenital pleural effusion may be secondary to various disorders. In majority of cases congenital pleural effusion is associated with hydops fetalis. Isolated pleural pleural effusion may be secondary to lymphatic abnormality. Most of isolated effusion present as chylous effusion. Isolated hemorrhagic and non chylous effusions are rare. Hemorrhagic effusion may present secondary to disseminated intravascular coagulation, hemorrhagic disease of newborn or trauma [4]. Our case has normal coagulation study and there was no history of trauma. There was no recollection of pleural fluid and the baby did very well after the drainage. That rules out any lymphatic, bronchial structural, or vascular anomalies. Congenital pleural effusion may present with severe pulmonary hypoplasia. When detected antenatally, an attempt should be made to dertemine the eitiology.

Competing Interests

The author declare that there is no competing interests regarding the publication of this article.


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