Introduction
Chylothorax and chylopericardium result from disruption of the thoracic duct or its tributaries. In children, they are most often post-operative complications of congenital heart surgery, with an incidence of 0.25–9% depending on procedure type. Reference Beghetti, La Scala, Belli, Bugmann, Le Coultre and Kalangos1 Traumatic chylothorax is rare in childhood, accounting for <3% of all paediatric cases. Reference Buttiker, Fanconi and Burger2 Reported mechanisms include blunt chest trauma, falls, seat-belt injuries, and penetrating trauma, but cases following low-energy blast injuries have not been described. Reference Doerr, Allen, Nichols and Ryu3–Reference Tutor5
We present a child with an atypical presentation after a minor firecracker explosion, complicated by massive chylopericardium and chylothorax, ultimately requiring thoracic duct embolisation after failure of conservative treatment.
Case presentation
An 11-year-old boy presented with sudden, painless swelling of the neck and upper chest after a firecracker exploded approximately one foot in front of his chest. The swelling involved both supraclavicular fossae without bruising, erythema, or external injury. He had no respiratory or systemic symptoms.
He was initially treated for suspected angioedema with dexamethasone and oral antibiotics, but swelling persisted. Examination revealed reduced breath sounds over the left hemithorax. Chest radiograph showed a widened mediastinum and a massive left pleural effusion (Figure 1). Echocardiography demonstrated a large pericardial effusion. CT confirmed bilateral pleural effusions, a large pericardial effusion, and mediastinal oedema.
Chest X-ray showing widened mediastinum and a large left pleural effusion. No bony fractures seen.

Figure 1 Long description
A chest X-ray showing widened mediastinum and a large left pleural effusion. The X-ray reveals no visible bony fractures. The image is labeled as a PA erect view, indicating it was taken in a posterior-anterior orientation with the patient standing. The left side of the chest appears more opaque due to the presence of fluid, suggesting a pleural effusion. The mediastinum, the central part of the chest that contains the heart, appears wider than usual, which could indicate various conditions, including fluid accumulation around the heart or enlargement of the heart itself.
Pigtail drains inserted into the pericardial and left pleural cavities yielded milky fluid. Biochemical testing confirmed chyle (pericardial triglycerides 4.2 mmol/L; pleural triglycerides 3.3 mmol/L). Cultures and cytology were negative.
Fasting lymphoscintigraphy demonstrated diffuse tracer accumulation in both lungs, suggesting chyle leakage into the pleural spaces, but could not localise a discrete thoracic duct injury.
Daily chyle drainage ranged between 20 and 30 mL/kg/day, peaking at 1.2 L/day. He was placed nil by mouth with total parenteral nutrition for two weeks, followed by a fat-free diet. Octreotide infusion was escalated to 4 µg/kg/min. Effusions initially resolved after three weeks but recurred.
A multidisciplinary team concluded that thoracic duct ligation would be unlikely to succeed because the leak site could not be identified. A pericardial–pleural window was created, but high-output drainage persisted despite five weeks of conservative therapy.
He subsequently underwent lymphangiography and thoracic duct embolisation performed by the paediatric interventional cardiology team. Due to unsuccessful bilateral inguinal lymph node access, retrograde thoracic duct cannulation was achieved via the right femoral vein. Using a 4 Fr JR catheter (Cordis, JL, USA), a Renegade microcatheter (Boston Scientific, MA, USA), and a 0.014″ Runthrough NS Extra Floppy coronary wire (Terumo, Tokyo, Japan), the thoracic duct was accessed at the junction of the left internal jugular and subclavian veins. Lipiodol injection demonstrated contrast leakage into the left pleural cavity. Because no focal leak could be identified, embolisation was performed above the cisterna chyli using 4 mm × 8 cm and 3 mm × 12 cm Interlock-18 coils (Boston Scientific, MA, USA) (Figure 2).
Angiographic images showing ( a ) retrograde cannulation of the thoracic duct from the left subclavian vein, ( b ) contrast leak into the left pleural cavity, and ( c ) coil embolisation of the thoracic duct.

Figure 2 Long description
An angiographic image showing retrograde cannulation of the thoracic duct from the left subclavian vein. The image includes three panels. The first panel shows the cannulation process with an arrow indicating the insertion point. The second panel shows a contrast leak into the left pleural cavity, highlighted by an arrow. The third panel shows coil embolization of the thoracic duct, with an arrow pointing to the embolized area.
Following the procedure, chyle output declined dramatically and ceased by day 3. The pigtail catheter was removed on day 5. At 5-month follow-up, he remained asymptomatic with no recurrence.
Discussion
Chylothorax and chylopericardium are uncommon in children, with post-operative aetiologies accounting for the majority of cases. In paediatric series, 50–70% of chylothoraces occur after congenital heart surgery, while 10–34% arise from congenital lymphatic abnormalities and fewer than 10% are associated with malignancy. Reference Beghetti, La Scala, Belli, Bugmann, Le Coultre and Kalangos1,Reference Buttiker, Fanconi and Burger2,Reference Tutor5 Traumatic chylothorax is distinctly rare, representing only 1–5% of paediatric cases and approximately 2% in larger mixed-age cohorts.[Reference Beghetti, La Scala, Belli, Bugmann, Le Coultre and Kalangos1–Reference McGrath, Blades and Anderson4] Most reported traumatic cases follow high-energy blunt mechanisms, particularly motor vehicle accidents and major deceleration injuries.[Reference McGrath, Blades and Anderson4] Low-energy traumatic mechanisms are exceptionally uncommon. Reference Tutor5–Reference Majdalany, Murthy and Jimenez8 Our case is therefore unusual, as a low-energy firecracker blast resulted in extensive lymphatic disruption leading to both chylothorax and chylopericardium.
The thoracic duct is anatomically vulnerable at the cervicothoracic junction, where it arches laterally to enter the left subclavian–internal jugular venous angle. Reference McGrath, Blades and Anderson4 Even minor acceleration–deceleration or traction forces can result in microdisruption of the duct at this site, predisposing to lymphatic leakage. Reference McGrath, Blades and Anderson4,Reference Tutor5 The acute swelling localised to the patient’s left neck and upper chest lies along this anatomical trajectory, further supporting a traumatic mechanism despite the apparently low-energy nature of the injury.
Accurate imaging is crucial for evaluating chylous effusions. Lymphoscintigraphy assesses functional lymphatic flow but rarely identifies specific leak sites due to low spatial resolution. Reference Tutor5 More advanced modalities, including intranodal lymphangiography and dynamic contrast magnetic resonance lymphangiography, allow detailed visualisation of central lymphatic anatomy and leakage points and are increasingly used to guide therapy. Reference Gómez, Baetens and Santos6,Reference Itkin and Nadolski7 Paediatric studies show high diagnostic yield with intranodal lymphangiography when conventional imaging is inconclusive. Reference Majdalany, Murthy and Jimenez8 In this case, lymphoscintigraphy confirmed leakage but could not localise the defect, and dynamic contrast magnetic resonance lymphangiography was unavailable, limiting surgical options.
Initial management of chylothorax focuses on conservative therapy, including pleural drainage, dietary fat restriction or nil enteral intake with total parenteral nutrition, and adjunctive agents such as octreotide. Reference Beghetti, La Scala, Belli, Bugmann, Le Coultre and Kalangos1,Reference Buttiker, Fanconi and Burger2,Reference Tutor5 While 70–80% of low-output chylothorax cases resolve with conservative therapy, high-output or persistent leaks often require escalation. Reference Beghetti, La Scala, Belli, Bugmann, Le Coultre and Kalangos1,Reference Buttiker, Fanconi and Burger2 Established guidelines emphasise considering interventional or surgical treatment early when drainage remains high despite optimal medical management. Reference Buttiker, Fanconi and Burger2,Reference Tutor5
Traditionally, thoracic duct ligation has been the definitive treatment for refractory chylothorax. Reference Buttiker, Fanconi and Burger2,Reference McGrath, Blades and Anderson4 However, the advent of minimally invasive lymphatic interventions—particularly thoracic duct embolisation—has transformed the therapeutic landscape. Reference Gómez, Baetens and Santos6,Reference Itkin and Nadolski7 Thoracic duct embolisation allows targeted occlusion of disrupted lymphatic channels with lower morbidity compared to surgery. Paediatric series have demonstrated high clinical success rates of thoracic duct embolisation in post-operative and traumatic chylothorax. Reference Majdalany, Murthy and Jimenez8,Reference Abdullah, Kakamad and Ahmed9
In our patient, the absence of a discrete leak during lymphangiographic evaluation precluded targeted embolisation. Nevertheless, proximal thoracic duct embolisation, performed just above the cisterna chyli, is an established alternative when the leak cannot be directly visualised, as it effectively halts antegrade lymphatic flow. Reference Gómez, Baetens and Santos6,Reference Itkin and Nadolski7 Despite lacking dedicated lymphatic interventional radiology services in our centre, the procedure was successfully performed by a team of paediatric interventional cardiologists. This highlights the adaptability of paediatric cardiology services in managing complex lymphatic disorders, particularly in institutions where interventional radiology lymphatic expertise is limited.
The rapid and sustained resolution of both chylothorax and chylopericardium aligns with growing paediatric evidence supporting thoracic duct embolisation as a safe and effective modality for refractory lymphatic leaks. Reference Gómez, Baetens and Santos6–Reference Abdullah, Kakamad and Ahmed9
Conclusions
Traumatic chylothorax and chylopericardium are rare in children and usually associated with high-energy trauma. This case demonstrates that even low-energy blast injuries can cause significant thoracic duct disruption. Persistent high-output drainage despite optimised conservative management should prompt early consideration of advanced lymphatic imaging and minimally invasive treatment. Thoracic duct embolisation is an effective alternative to surgical ligation and should be considered when conservative measures fail or leak localisation is uncertain.
Acknowledgements
The authors acknowledge Dr Koh Ghee Tiong, Dr Shereen Toh, Dr Pon Kah Min, and Dr Nurul Amani Abd Ghani for their joint management of the patient.
Financial support
This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.
Competing interests
None.