Abstract | INTRODUCTION:
Chylothorax is a rare complication of surgical neck dissection. This is the first reported pediatric case of bilateral chylothorax following cervical surgery and the first to occur after tracheoplasty. Chylothorax can lead to significant complications, including hypoxemia and shock, and requires timely treatment. This case report discusses the clinical presentation, diagnosis, and treatment of our patient and reviews possible pathophysiologic mechanisms to explain the development of postoperative bilateral chylous effusions. CASE PRESENTATION: CONCLUSIONS: Massive bilateral chylothorax is a rare but potentially life-threatening complication following tracheoplasty. Clinicians caring for this patient population postoperatively should be aware of this potential complication and its management.
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Authors | Aaron L Thatcher, Jane Yu, Kevin W Kuo |
Journal | Journal of medical case reports
(J Med Case Rep)
Vol. 9
Pg. 235
(Oct 22 2015)
ISSN: 1752-1947 [Electronic] England |
PMID | 26493840
(Publication Type: Case Reports, Journal Article)
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Topics |
- Chylothorax
(diagnosis, therapy)
- Drainage
- Female
- Heart Failure
(surgery)
- Humans
- Hypoxia
(etiology)
- Infant
- Neck Dissection
(adverse effects)
- Postoperative Complications
(diagnosis)
- Reoperation
- Shock
(etiology)
- Thoracic Duct
(surgery)
- Tracheobronchomalacia
(surgery)
- Tracheostomy
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