TY - JOUR
T1 - Chylous ascites
T2 - A review of pathogenesis, diagnosis and treatment
AU - Bhardwaj, Richa
AU - Vaziri, Haleh
AU - Gautam, Arun
AU - Ballesteros, Enrique
AU - Karimeddini, David
AU - Wu, George Y.
N1 - Publisher Copyright:
© 2018 Authors.
PY - 2018
Y1 - 2018
N2 - Chylous ascites (CA) is a rare form of ascites that results from the leakage of lipid-rich lymph into the peritoneal cavity. This usually occurs due to trauma and rupture of the lymphatics or increased peritoneal lymphatic pressure secondary to obstruc-tion. The underlying etiologies for CA have been classified as traumatic, congenital, infectious, neoplastic, postoperative, cirrhotic or cardiogenic. Since malignancy and cirrhosis ac-count for about two-thirds of all the cases of CA in Western countries, in this article we have attempted to reclassify CA based on portal and non-portal etiologies. The diagnosis of CA is based on the distinct characteristic of the ascitic fluid which includes a milky appearance and a triglyceride level of >200 mg/dL. The management consists of identifying and treating the underlying disease process, dietary modification, and diuretics. Some studies have also supported the use of agents such as orlistat, somatostatin, octreotide and etilefrine. Para-centesis and surgical interventions in the form of transjugular intrahepatic portosystemic shunt (commonly known as TIPS), peritoneal shunt, angiography with embolization of a leaking vessel, and laparotomy remain as treatment options for cases refractory to medical management.
AB - Chylous ascites (CA) is a rare form of ascites that results from the leakage of lipid-rich lymph into the peritoneal cavity. This usually occurs due to trauma and rupture of the lymphatics or increased peritoneal lymphatic pressure secondary to obstruc-tion. The underlying etiologies for CA have been classified as traumatic, congenital, infectious, neoplastic, postoperative, cirrhotic or cardiogenic. Since malignancy and cirrhosis ac-count for about two-thirds of all the cases of CA in Western countries, in this article we have attempted to reclassify CA based on portal and non-portal etiologies. The diagnosis of CA is based on the distinct characteristic of the ascitic fluid which includes a milky appearance and a triglyceride level of >200 mg/dL. The management consists of identifying and treating the underlying disease process, dietary modification, and diuretics. Some studies have also supported the use of agents such as orlistat, somatostatin, octreotide and etilefrine. Para-centesis and surgical interventions in the form of transjugular intrahepatic portosystemic shunt (commonly known as TIPS), peritoneal shunt, angiography with embolization of a leaking vessel, and laparotomy remain as treatment options for cases refractory to medical management.
KW - Ascitic fluid
KW - Chylous ascites
KW - Cirrhosis
KW - Lymphatic system
KW - Portal hypertension
UR - http://www.scopus.com/inward/record.url?scp=85053412430&partnerID=8YFLogxK
U2 - 10.14218/JCTH.2017.00035
DO - 10.14218/JCTH.2017.00035
M3 - Review article
AN - SCOPUS:85053412430
SN - 2225-0719
VL - 6
SP - 105
EP - 113
JO - Journal of Clinical and Translational Hepatology
JF - Journal of Clinical and Translational Hepatology
IS - 1
ER -