Steatorrhea

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(Redirected from Steatorrhoea)

Steatorrhea is a medical condition characterized by the excessive excretion of fat in feces. This page will elaborate on the causes, symptoms, diagnosis, and treatment of this condition, providing an in-depth understanding for medical students.

Introduction[edit | edit source]

Steatorrhea is a condition that manifests as an abnormally high fat content in the feces. The stools may appear pale, oily, and unusually foul-smelling. The condition is typically indicative of underlying malabsorption disorders, where the body is unable to absorb fats and other nutrients from the gastrointestinal tract properly.[1]

Etiology[edit | edit source]

The causes of steatorrhea are usually diseases or conditions that affect the body's ability to absorb fat from the diet. This can include diseases of the pancreas (like chronic pancreatitis), liver diseases (such as cirrhosis), or diseases that affect the lining of the intestines (like celiac disease or Crohn's disease).[2]

Symptoms[edit | edit source]

The most notable symptom of steatorrhea is bulky, foul-smelling stools that appear pale and oily. They may be difficult to flush away and can leave a greasy residue in the toilet. Other associated symptoms may include weight loss, diarrhea, and signs of malnutrition.[3]

Diagnosis[edit | edit source]

The diagnosis of steatorrhea typically involves analyzing a stool sample to measure its fat content. A 72-hour fecal fat test is often used, which involves collecting all feces passed over 72 hours for analysis. Blood tests may also be used to check for nutritional deficiencies, and imaging studies or endoscopic procedures may be used to investigate the health of the gastrointestinal tract.[4]

Management and Treatment[edit | edit source]

Treatment for steatorrhea primarily involves managing the underlying cause. For diseases like celiac or Crohn's, a change in diet may be necessary. In cases where the pancreas is not producing enough digestive enzymes, Pancreatic enzyme replacement therapy (PERT) may be prescribed. Fat-soluble vitamin supplements may also be needed if malabsorption has led to deficiencies.[5]

See also[edit | edit source]

References[edit | edit source]

  1. Othman MO, Harb D, Barkin JA. Introduction and Overview of Therapeutic Endoscopy. Gastrointestinal Endoscopy Clinics, 2016.
  2. Lindkvist B. Diagnosis and treatment of pancreatic exocrine insufficiency. World Journal of Gastroenterology, 2013.
  3. Van de Vijver E, Desager K, Mulberg AE, et al. Treatment of infants and toddlers with cystic fibrosis-related pancreatic insufficiency and fat malabsorption with pancrelipase MT. Journal of Pediatric Gastroenterology and Nutrition, 2011.
  4. Leeds JS, Hopper AD, Hurlstone DP, et al. Is exocrine pancreatic insufficiency in adult coeliac disease a cause of persisting symptoms? Alimentary Pharmacology & Therapeutics, 2007.
  5. Domínguez-Muñoz JE. Pancreatic enzyme replacement therapy for pancreatic exocrine insufficiency: when is it indicated, what is the goal and how to do it? Advances in Medical Sciences, 2011.

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Contributors: Prab R. Tumpati, MD