Chronic liver failure/cirrhosis
Protein-losing enteropathy (PLE) (see Table 16-1 for differential diagnosis)
Pancreatitis
Bacterial peritonitis
Chronic tuberculous peritonitis
Congenital TORCH infection: toxoplasmosis, other, rubella, cytomegalovirus, and herpes simplex virus
Hodgkin disease
Intraperitoneal tumor
Hepatic vein occlusion (Budd-Chiari syndrome, veno-occlusive disease)
Portal vein obstruction/portal hypertension
Renal vein thrombosis
Congestive heart failure
Thoracic duct obstruction (chylous ascites)
Lysosomal storage disease
Chronic adhesive pericarditis
Peritonitis—rheumatic, meconium, bile
Nephrotic syndrome
Perforation of the urinary tract
Obstructive uropathy
Acute glomerulonephritis
Chronic renal failure
Systemic lupus erythematosus
Familial Mediterranean fever
Maternal diabetes
Enlarged lymph node
Pulmonary lymphangiectasia
Malnutrition
or fever. Fluid should be obtained for cell count and differential, gram stain and culture, and albumin concentration. Serum-ascites albumin gradient (SAAG), the difference in albumin concentration between serum and ascitic fluid, is a useful measurement that dividing ascites into two categories—high gradient (>1.1 g/dL) and low gradient (<1.1 g/dL). High gradient SAAG is suggestive of portal hypertension, most suggestive of cirrhosis, heart failure, fulminant hepatic failure, and hepatic venous outflow obstruction (Budd-Chiari or veno-occlusive disease). Low-gradient ascites suggests conditions without portal hypertension, such as pancreatic ascites, tuberculous ascites, peritoneal carcinomatosis, and nephrotic syndrome. The SAAG is a superior measure compared to total protein of the fluid in differentiating cases of portal hypertension.
TABLE 16-1 Diseases Associated with Enteric Protein Loss | |||||||||||||||||||||||||
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