S6458 Diagnostic Challenges in Chylous Ascites: A Case Report of Suspected Lymphatic Obstruction Following Distal Gastrectomy and Vagotomy

Introduction: Chylous ascites (CA) is a rare condition characterized by triglyceride-rich, milky peritoneal fluid. It can arise from trauma, malignancies, infections, or abdominal surgery complications, leading to chronic leakage, immune suppression, and malnutrition. With a mortality rate of 40 to 70%, early diagnosis and treatment are vital. This case discusses a patient with newly diagnosed CA, with at least a 2-year delay in diagnosis following his initial presentation. Case Description/Methods: We present the case of a 61-year-old man with a history of lymphedema, alcohol use disorder, and perforated peptic ulcer disease repaired by distal gastrectomy and vagotomy in 2013 who presented with worsening dyspnea, bilateral lower extremity edema, and ascites. Previously managed with paracentesis and diuretics for presumed alcohol-related cirrhosis, his condition progressed to monthly taps despite therapy, developing severe lymphedema, scrotal swelling, and ascites. Lab findings showed chronic hypoalbuminemia, hypocalcemia, and a Model for End-Stage Liver Disease-3.0 score of 11. Abdominal ultrasound revealed large-volume ascites and a possible micronodular liver contour. Ascitic fluid analysis (serum-albumin ascites gradient <0.5, protein levels <1.0 g/dL) excluded portal hypertension or cardiac disease. Subsequent paracentesis revealed 4 liters of milky fluid (triglycerides >1,050 mg/dL). Follow-up interventional radiology-lymphangiography revealed dilated lymphatic channels, but no apparent leak. He was discharged on an optimized diuretic and nutritional regimen, with instructions for outpatient follow-up to undergo MR lymphangiography to evaluate for lymphatic disruption and identify potential areas for therapeutic intervention. Discussion: CA is a rare accumulation of triglyceride-rich peritoneal fluid, often due to malignancy, cirrhosis, or infections. In our patient, asymmetric lymphedema following distal gastrectomy and vagotomy, along with fatty ascites, suggests postoperative lymphatic obstruction, an underrecognized cause of CA. Early diagnostic paracentesis (e.g., triglycerides >220 mg/dL) is crucial to prevent malnutrition and immunodeficiency. Computerized tomography may reveal ductal injury, while lymphangiography localizes leaks for intervention. Prognosis varies by etiology, with high mortality if surgical or oncologic interventions aren’t feasible. Further magnetic resonance lymphangiography or lymphoscintigraphy, carcinoembryonic antigen tests, and infectious workup are necessary to exclude malignancy or infection and strategize treatment.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001154292.29643.b4
Primary Topic
Lymphatic Disorders and Treatments
Type
article
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article

S6458 Diagnostic Challenges in Chylous Ascites: A Case Report of Suspected Lymphatic Obstruction Following Distal Gastrectomy and Vagotomy

The American Journal of Gastroenterology
Lymphatic Disorders and Treatments
article

S6458 Diagnostic Challenges in Chylous Ascites: A Case Report of Suspected Lymphatic Obstruction Following Distal Gastrectomy and Vagotomy

article en

Abstract

Introduction: Chylous ascites (CA) is a rare condition characterized by triglyceride-rich, milky peritoneal fluid. It can arise from trauma, malignancies, infections, or abdominal surgery complications, leading to chronic leakage, immune suppression, and malnutrition. With a mortality rate of 40 to 70%, early diagnosis and treatment are vital. This case discusses a patient with newly diagnosed CA, with at least a 2-year delay in diagnosis following his initial presentation. Case Description/Methods: We present the case of a 61-year-old man with a history of lymphedema, alcohol use disorder, and perforated peptic ulcer disease repaired by distal gastrectomy and vagotomy in 2013 who presented with worsening dyspnea, bilateral lower extremity edema, and ascites. Previously managed with paracentesis and diuretics for presumed alcohol-related cirrhosis, his condition progressed to monthly taps despite therapy, developing severe lymphedema, scrotal swelling, and ascites. Lab findings showed chronic hypoalbuminemia, hypocalcemia, and a Model for End-Stage Liver Disease-3.0 score of 11. Abdominal ultrasound revealed large-volume ascites and a possible micronodular liver contour. Ascitic fluid analysis (serum-albumin ascites gradient <0.5, protein levels <1.0 g/dL) excluded portal hypertension or cardiac disease. Subsequent paracentesis revealed 4 liters of milky fluid (triglycerides >1,050 mg/dL). Follow-up interventional radiology-lymphangiography revealed dilated lymphatic channels, but no apparent leak. He was discharged on an optimized diuretic and nutritional regimen, with instructions for outpatient follow-up to undergo MR lymphangiography to evaluate for lymphatic disruption and identify potential areas for therapeutic intervention. Discussion: CA is a rare accumulation of triglyceride-rich peritoneal fluid, often due to malignancy, cirrhosis, or infections. In our patient, asymmetric lymphedema following distal gastrectomy and vagotomy, along with fatty ascites, suggests postoperative lymphatic obstruction, an underrecognized cause of CA. Early diagnostic paracentesis (e.g., triglycerides >220 mg/dL) is crucial to prevent malnutrition and immunodeficiency. Computerized tomography may reveal ductal injury, while lymphangiography localizes leaks for intervention. Prognosis varies by etiology, with high mortality if surgical or oncologic interventions aren’t feasible. Further magnetic resonance lymphangiography or lymphoscintigraphy, carcinoembryonic antigen tests, and infectious workup are necessary to exclude malignancy or infection and strategize treatment.

The American Journal of GastroenterologyVol. 120(10S2)
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Lymphatic Disorders and Treatments
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