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ULY CLINIC

ULY CLINIC

18 Septemba 2025, 13:23:52

Clay-colored stools

Clay-colored stools
Clay-colored stools
Clay-colored stools

Clay-colored stools are pale, putty-like stools that typically result from hepatic, gallbladder, or pancreatic disorders. Normally, bile pigments give stool its characteristic brown color. Hepatocellular dysfunction or biliary obstruction interferes with bile pigment secretion, leading to clay-colored stools. These stools often accompany jaundice and dark “cola-colored” urine.


History and Physical Examination

History
  • Document onset of clay-colored stools.

  • Explore associated symptoms: abdominal pain, nausea, vomiting, fatigue, anorexia, weight loss, dark urine.

  • Assess digestive tolerance, e.g., difficulty with fatty or heavy meals.

  • Evaluate bleeding tendencies and previous biliary, hepatic, or pancreatic disorders.

  • Ask about biliary surgery, barium studies, antacid use, alcohol intake, and hepatotoxin exposure.


Physical Examination
  • General appearance and vital signs.

  • Inspect skin and eyes for jaundice.

  • Abdomen: inspect for distention and ascites, auscultate bowel sounds, percuss, and palpate for masses or tenderness.

  • Obtain urine and stool specimens for laboratory analysis.


Medical causes

Cause

Key Features

Associated Signs/Symptoms

Bile duct cancer

Obstructive lesion

Jaundice, pruritus, anorexia, weight loss, upper abdominal pain, palpable mass, bleeding tendencies

Biliary cirrhosis

Progressive cholestatic disorder

Pruritus (worse at night), weakness, fatigue, weight loss, abdominal pain, jaundice, hyperpigmentation, malabsorption (steatorrhea, nocturnal diarrhea), hepatomegaly, hematemesis, ascites, edema, xanthomas

Sclerosing cholangitis

Chronic bile duct fibrosis

Clay-colored stools, intermittent jaundice, pruritus, right upper quadrant pain, fever, chills

Cholelithiasis/Choledocholithiasis

Stones causing obstruction

Intermittent clay-colored stools, biliary colic (RUQ pain radiating to shoulder), nausea, vomiting, tachycardia, fever, jaundice

Hepatic cancer

Tumor compressing bile flow

Weight loss, weakness, anorexia, firm hepatomegaly, jaundice, RUQ pain, ascites, dependent edema, fever, auscultatory bruits

Hepatitis (viral)

Icteric phase onset

Clay-colored stools, jaundice within 1–5 days, dark urine, anorexia, tender hepatomegaly, RUQ pain, splenomegaly, cervical lymphadenopathy, pruritus, post-icteric fatigue

Cholestatic nonviral hepatitis

Drug or toxin-induced

Similar to viral hepatitis: clay-colored stools, jaundice, fatigue, anorexia

Pancreatic cancer

Common bile duct obstruction

Clay-colored stools, abdominal/back pain, jaundice, pruritus, nausea, vomiting, anorexia, weight loss, fatigue, splenomegaly, GI bleeding, periumbilical bruit

Acute pancreatitis

Inflammatory disorder

Clay-colored stools, dark urine, jaundice, severe epigastric pain radiating to back, nausea, vomiting, fever, hypoactive bowel sounds, abdominal rigidity, crackles at lung bases, restlessness, tachycardia, mottled skin

Other causes

Biliary surgery: May cause bile duct strictures, leading to clay-colored stools.


Special considerations

  • Prepare for diagnostic tests:

    • Liver function tests, serum bilirubin

    • Hepatitis panels

    • Abdominal ultrasound, CT scan

    • Endoscopy, ERCP

    • Stool analysis


Patient counseling

  • Explain the importance of dietary modifications.

  • Advise avoiding alcohol and hepatotoxic substances.

  • Emphasize rest and measures to reduce abdominal pain.


Pediatric pointers

Infants may develop clay-colored stools due to biliary atresia.


Geriatric pointers

Elderly patients with cholelithiasis have a higher risk of complications; early surgical intervention should be considered for persistent symptoms.


References
  1. Berkowitz CD. Berkowitz’s Pediatrics: A Primary Care Approach. 4th ed. American Academy of Pediatrics; 2012.

  2. Buttaro TM, Tybulski J, Bailey PP, Sandberg-Cook J. Primary Care: A Collaborative Practice. Mosby Elsevier; 2008.

  3. McCance KL, Huether SE, Brashers VL, Rote NS. Pathophysiology: The Biologic Basis for Disease in Adults and Children. Mosby Elsevier; 2010.

  4. Sommers MS, Brunner LS. Pocket Diseases. F.A. Davis; 2012.

  5. Schiff ER, Maddrey WC, Sorrell MF. Schiff’s Diseases of the Liver. 12th ed. Wiley; 2017.

  6. Boyer TD, Manns MP, Sanyal AJ. Zakim and Boyer’s Hepatology: A Textbook of Liver Disease. 8th ed. Elsevier; 2021.

  7. McCance KL, Huether SE. Pathophysiology: The Biologic Basis for Disease in Adults and Children. 8th ed. Elsevier; 2019.

  8. Sleisenger MH, Fordtran JS. Sleisenger and Fordtran’s Gastrointestinal and Liver Disease. 11th ed. Elsevier; 2021.

  9. Berkowitz CD. Berkowitz’s Pediatrics: A Primary Care Approach. 4th ed. American Academy of Pediatrics; 2012.

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