2017
DOI: 10.1111/apt.14284
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Review article: the diagnostic approach and current management of chylous ascites

Abstract: SummaryBackground: Chylous ascites is rare, accounting for less than 1% of cases. An appropriate and stepwise approach to its diagnosis and management is of key importance.Aim: To review the current diagnostic approach and management of chylous ascites.Methods: A literature search was conducted using PubMed using the key words 'chylous', 'ascites', 'cirrhosis', 'pathophysiology', 'nutritional therapy', 'paracentesis", "transjugular intrahepatic portosystemic shunt" and "TIPSS'. Only articles in English were in… Show more

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Cited by 122 publications
(181 citation statements)
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“…Chylous ascites, an uncommon entity, is characterized by presence of milky peritoneal fluid abundant in triglycerides, nutrients and immunoglobulins resulting from congenital or acquired abnormalities of abdominal lymphatics. Although various etiologies have been described that result in this clinical entity, v.i.z, malignancy, infection, abdominal surgery, trauma, cirrhosis among others, the condition is uncommon and chylous ascites accounts for a very small number of overall ascites cases and as per published literature the current incidence is 1 case per 20,000 admissions (1).…”
Section: Introductionmentioning
confidence: 99%
“…Chylous ascites, an uncommon entity, is characterized by presence of milky peritoneal fluid abundant in triglycerides, nutrients and immunoglobulins resulting from congenital or acquired abnormalities of abdominal lymphatics. Although various etiologies have been described that result in this clinical entity, v.i.z, malignancy, infection, abdominal surgery, trauma, cirrhosis among others, the condition is uncommon and chylous ascites accounts for a very small number of overall ascites cases and as per published literature the current incidence is 1 case per 20,000 admissions (1).…”
Section: Introductionmentioning
confidence: 99%
“…4 The disease affected this patient's vaginal wall, leading to chylous vaginal discharge; it affected her intestines, leading to hypoproteinemia and protein-losing enteropathy (Fig 2); and her retroperitoneal tissue was also affected by an asymptomatic macrocystic lymphatic malformation (Fig 1). Except for the chylous discharge, congenital chylorrhea (eg, GLA) can occur anywhere in the body and may be manifested as scrotal chylorrhea, 9,10 lymphedema of external genitalia, 11 chylothorax, 12,13 chylous ascites, 14,15 or chylopericardium. 16 T2-weighted MRI showed diffuse intestinal lesions (Fig 2), and the blood tests found hypoproteinemia, which indicated intestinal lymphangiectasia and protein-losing enteropathy in this patient.…”
Section: Discussionmentioning
confidence: 99%
“…Total parenteral nutrition has been described as the method of choice for nutritional therapy as enteral nutrition promotes the formation of chyle. The administration of octreotide reduces intestinal fat absorption, concentration of triglycerides in the thoracic duct and in lymphatic vessel flow [16,31,32], although some reports does not agree with this concept [33].…”
Section: Discussionmentioning
confidence: 99%