Delayed concurrent chylothorax and chyloperitoneum: report of a case after an old blunt trauma
Mohsen Sokouti1, Babak Abri Aghdam1
1Department of Thoracic Surgery, Imam Reza Hospital, Tabriz University of Medical Sciences, TABRIZ - IRAN.
Insights
A rare thoracic duct cyst caused prolonged chylothorax and chyloperitoneum in a 15-year-old boy. Transabdominal thoracic duct ligation successfully resolved the condition, offering a potential treatment choice.
Area of Science:
- Thoracic Surgery
- Pediatric Surgery
- Gastrointestinal Surgery
Background:
- Chylothorax, characterized by chyle-rich fluid in the pleural space, presents a significant clinical challenge, particularly when refractory to initial treatments.
- Mediastinal cysts can cause delayed complications, including persistent chylothorax, necessitating advanced diagnostic and therapeutic approaches.
Observation:
- A 15-year-old male presented with a 40-day history of right chylothorax and respiratory distress, unresponsive to conventional management.
- Computed Tomography revealed a large left posterior mediastinal cyst with left pleural effusion, complicating the initial right-sided presentation.
- Exploratory laparotomy identified chyloperitoneum and confirmed the need for thoracic duct intervention.
Findings:
- Initial right thoracotomy and thoracic duct ligation failed to resolve the chylothorax, which worsened post-operatively.
- Transabdominal ligation of the thoracic duct below the diaphragm proved effective, resolving right chylothorax within 1-2 days.
- Left chylous effusion gradually decreased, with complete resolution achieved 46 days post-laparotomy, and the patient showed excellent recovery at one-year follow-up.
Implications:
- This case highlights a unique presentation of a thoracic duct cyst leading to delayed chylothorax and chyloperitoneum, a combination not previously reported.
- Transabdominal thoracic duct ligation is presented as a viable and effective surgical option for complex and refractory chylothorax cases.
- The successful management underscores the importance of considering rare anatomical anomalies and adapting surgical strategies for challenging pediatric thoracic conditions.
Abstract:
A 15- year-old boy was referred to Imam Reza Hospital with a right chest tube and chylothorax for 40 days. The patient had respiratory distress and undergone refractory treatment for chylothorax. The fluid content was chyle-rich in lipids. Computed Tomography of the chest showed a large, incompletely evacuated cyst in the left posterior mediastinum with left pleural effusion. The cyst could not be resected through right thoracotomy, because of the left side location of the cyst. Ligation of the thoracic duct through right thoracotomy was not effective in reducing chylous effusion 4 days later. Left chylothorax exacerbated because of the complication of right thoracotomy. Laparatomy was performed to ligate the thoracic duct 6 days later. On exploratory laparatomy, chylous effusion was detected in the peritoneum. Thoracic duct with all the fibro-fatty tissues was ligated below the diaphragm over the spine at 12(th) to 2(nd) vertebral spaces. Right chylothorax was resolved after ligation of thoracic duct transabdominally 1-2 days later. Left chylous effusion was decreased and treated 46 days after laparatomy. One year follow up of the patient showed excellent result. In our knowledge, thoracic duct cyst occurring as a result of a delayed chylothorax and chyloperitoneum has not been reported in the literature. Surgical thoracic duct ligation can be the treatment of choice.
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