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Home » Malabsorption Syndrome: Causes, Symptoms, Diagnosis and Management

Malabsorption Syndrome: Causes, Symptoms, Diagnosis and Management

August 31, 2025 by Marksparks .arkansas Leave a Comment

Malabsorption Syndrome: Causes, Symptoms, Diagnosis & Management

Question. Write a Short Note On Malabsorption Syndrome.
Or
What Is Malabsorption Syndrome, Causes Of Malabsorption, Clinical Features, And Its Management?

Answer. Malabsorption syndrome comprises a large number of pathological conditions in which there is a disturbance of processes by which nutrients are transferred from the lumen of the intestine into circulation.

“Understanding malabsorption syndrome through FAQs: Causes, symptoms, diagnosis, and management explained”

Etiology of Malabsorption

  • Stomach:
    • Precipitate emptying after postgastrectomy dumping.
    • Lack of intrinsic factor.
    • Excess acid secretion in Zollinger­Ellison syndrome.
  • Pancreatic: Inadequate enzyme and bicarbonate secretion.
  • Biliary: Due to defective micelle formation.
  • Endocrine diseases
  • Parasitic or drug.
    Various diseases, along with their etiologies, can cause malabsorption as:
  • Disorders of intraluminal digestion
    • Pancreatic enzyme deficiency in chronic pancreatitis, cystic fibrosis, and pancreatic carcinoma
    • Disturbances of gastric function after gastroenterostomy and partial gastrectomy
    • Deficiency of bile acids in Crohn’s disease, resection of the terminal ileum, stagnant loop syndrome, or blind loop syndrome.
  • Disorders of transport in the intestinal mucosal cell
    • With histologically abnormal mucosa (infiltration, inflammation, or infection of mucosa) in coeliac disease, tropical sprue, lymphoma, Whipple’s disease, giardiasis and radiation enteritis
    • With histologically normal mucosa (genetic diseases) in lactase deficiency, pernicious anemia
    • Disorders of transport from mucosal cells in abdominal lymphoma, tuberculosis, telangiectasia of mesenteric lymphatics, beta hypoproteinemia,
    • Impaired nutrient uptake in lymphatic obstruction, cardiac heart failure, and pericarditis
    • Miscellaneous: Diabetes mellitus, hyperthyroidism, hyperparathyroidism

“Factors influencing success with malabsorption syndrome knowledge: Q&A”

Clinical Features of Intestinal Mucosal Cell

  • *Steatorrhea presents symptoms.
  • Diarrhea or abdominal discomfort.
  • Nutritional deficiencies, i.e., deficiency of vitamins A, D, B12, and K
  • General features include anemia, sore mouth, loss of weight, fatigue, and lethargy.
  • Bone pain may be present.
  • Skin changes like pellagra are present
  • The patient also suffers from peripheral neuropathy, irritability, and lack of confidence.

“Common challenges in diagnosing and managing malabsorption syndrome effectively: FAQs provided”

Investigations of intestinal mucosal cells

Tests are carried out to detect nutritional deficiencies.
These tests indicate the malabsorption of a particular nutrient and not its cause.

  • Fecal fat stimulation: It confirms steatorrhea and fat malabsorption.
    Sudan III stain may show an increase in stool fat. Quantitative estimation of fat in the stool is more reliable and sensitive.
    A 72­hour stool collection while the patient is on a defined diet is used for fat estimation.
    Excretion of more than 10 g of fat per day suggests fat malabsorption.
  • Schilling test: This is useful in the diagnosis of cobalamin (B12) malabsorption and its causes, like pernicious anemia, chronic pancreatitis, achlorhydria, and bacterial
    overgrowth. In this test, radio­labelled cobalamin (l mg 68°C) should be given orally, and its excretion in urine is measured. 1 mg cobalamin is administered intramuscularly to saturate hepatic binding sites so that all radiolabelled cobalamin is excreted in the urine.
    The test is abnormal if less than l0% of the radio­labelled cobalamin is excreted in the urine in 24 hours.
    This will help in differentiating the various defects responsible for the malabsorption of cobalamin.

“Steps to explain malabsorption syndrome: Causes vs symptoms vs diagnosis vs management: Q&A guide”

  • D-xylose test: It detects carbohydrate malabsorption. 25 g of D­xylose is given orally, and its excretion is measured in urine.
    Excretion of less than 4.5 g in 5 hours is suggestive of malabsorption.
  • Upper gastrointestinal endoscopy and biopsy of small intestinal mucosa: It is essential for the diagnosis of conditions like tropical sprue, celiac sprue, Whipple’s disease, and Crohn’s
    disease.
  • Barium meal contrast radiography: Radiological assessment of the small intestine with barium contrast is helpful in the evaluation of structural abnormalities in Crohn’s disease,
    diverticulae and strictures.
  • Pancreatic exocrine functions: They should be carried out in patients with steatorrhea.
  • Serological studies: In some of the conditions, such as celiac sprue and pernicious anemia, autoantibodies are detected.
  • Small intestinal biopsy (duodenal or jejunal): It is carried out for diagnostic purposes.

“Importance of studying malabsorption syndrome for healthcare professionals: Questions explained”

Management of the intestinal mucosal cell

  • Diet: A high-protein and low-fat diet is taken.
  • Digestants: Pancreatic enzyme preparations are administered after meals.
  • Treatment of anemia: All three hematinic vitamins B12, folic acid, and iron are given.
  • Vitamin supplements: Vitamin B complex and vitamin D are given.
  • Treatment of diarrhea: Codeine and loperamide are administered.
  • Steroids: Prolonged therapy with prednisolone is given.
  • Elimination of bacterial overgrowth: Tetracycline 250 mg TDS for one week.

Filed Under: General Medicine

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