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Thoracic Cavernous Lymphangioma Provoking Massive Chyloptysis: A Case Report
Robert Ferguson1, Jeffrey Hodges1, Cayce Harness-Brumley1
1University of Texas Southwestern, Dallas, TX, USA.
Journal of Investigative Medicine High Impact Case Reports
|October 2, 2015
Summary
Chyloptysis, or milky sputum, is rare. This case highlights a young woman with massive chyloptysis from a peripartum thoracic lymphangioma, requiring cardiopulmonary bypass for resection.
Area of Science:
- Thoracic Surgery
- Vascular Anomalies
- Pulmonary Medicine
Background:
- Chyloptysis is a rare condition with a broad differential diagnosis, presenting significant diagnostic and therapeutic challenges.
- Lymphangiomas are benign tumors of lymphatic vessels, and thoracic involvement can be life-threatening.
- Peripartum onset of thoracic masses can complicate management due to physiological changes during pregnancy and postpartum.
Purpose of the Study:
- To report a unique case of massive chyloptysis in a young woman.
- To describe the etiology of the chyloptysis as a thoracic cavernous lymphangioma.
- To detail the complex surgical management involving cardiopulmonary bypass.
Main Methods:
- Case presentation of a young woman with symptomatic chyloptysis.
- Diagnostic workup including imaging to identify the thoracic mass.
- Surgical resection of the thoracic lymphangioma utilizing cardiopulmonary bypass.
Main Results:
- Successful identification and resection of a large thoracic cavernous lymphangioma.
- Resolution of massive chyloptysis following surgical intervention.
- The patient's condition necessitated cardiopulmonary bypass due to the tumor's extent and location.
Conclusions:
- Thoracic cavernous lymphangioma can present with massive chyloptysis, particularly in the peripartum period.
- Surgical resection, even with cardiopulmonary bypass, can be a viable treatment for life-threatening chyloptysis.
- This case represents a unique clinical scenario in the literature regarding etiology and management.
