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The basic workup includes a CBC, a blood smear for cell morphology, sedimentation rate, urinalysis, chemistry panel, serum B 12 and folic acid, serum amylase and lipase, stool for occult blood, ovum and parasites, fat and trypsin, and urine for 5-HIAA.
A sweat test should be done if cystic fibrosis is suspected. A d -xylose absorption test will help differentiate primary diseases of the small intestines. An abnormal yield of labeled carbon dioxide after ingestion of a meal with radioactive 14 C-glycocholate will help diagnose bacterial overgrowth. An upper GI series and small bowel follow-through may be helpful. Intubation and analysis of pancreatic secretion of enzymes after pancreozymin or secretin injection will help differentiate pancreatic disorders. A CT scan of the abdomen and endoscopy may be useful. Intestinal biopsy with a Crosby capsule may help differentiate primary intestinal diseases also. Consult a gastroenterologist before ordering many of these expensive diagnostic tests.
A therapeutic trial with pancreatic enzymes, antibiotics, or even a gluten-free diet may also assist in the diagnosis.
Read excerpts from these other book chapters related to Steatorrhea:
Copyright Details: Algorithmic Diagnosis of Symptoms and Signs, Copyright © 2008 Williams & Wilkins.
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More About This Book:
Title: Algorithmic Diagnosis of Symptoms and Signs Authors: R. Douglas Collins Publisher: Lippincott Williams & Wilkins Copyright: 2003 ISBN: 0-7817-3805-9
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