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Cystic fibrosis with other intestinal manifestations Save


ICD-10 code: E84.19

Disease category: None

Cystic Fibrosis with Other Intestinal Manifestations

Cystic fibrosis (CF) is a genetic disorder that primarily affects the lungs and digestive system. While the respiratory symptoms of CF are widely known, it's important to understand that the condition can also lead to various intestinal manifestations. These additional complications can have a significant impact on the quality of life for individuals with CF.

1. Meconium Ileus:

Meconium ileus is a common intestinal manifestation in newborns with CF. It occurs when the meconium, the first stool of an infant, becomes thick and sticky, blocking the intestines. This condition often requires surgical intervention to remove the obstruction and restore proper bowel function.

2. Intestinal Obstruction:

Individuals with CF are at a higher risk of developing intestinal obstructions due to the abnormal thickening of mucus in the digestive system. These obstructions can cause severe abdominal pain, bloating, and vomiting. Surgery may be necessary to alleviate the blockage and ensure proper digestion.

3. Intestinal Inflammation:

Chronic inflammation of the intestines, known as enteritis, is another common manifestation in CF patients. This inflammation can lead to diarrhea, malnutrition, and weight loss. Close monitoring, dietary adjustments, and specialized treatments are often required to manage this condition effectively.

4. Rectal Prolapse:

Rectal prolapse occurs when the rectum protrudes through the anus. CF-related digestive issues, such as chronic coughing, constipation, and increased abdominal pressure, can contribute to the development of this condition. Treatment options include lifestyle modifications, medication, or surgery, depending on the severity.

  1. 5. Intestinal Polyps:
  2. Individuals with CF are at an increased risk of developing intestinal polyps, which are abnormal tissue growths in the lining of the intestines. Regular screening is crucial to detect and remove these polyps early, reducing the risk of complications such as bleeding or obstruction.

It is important for individuals with CF and their caregivers to be aware of these potential intestinal manifestations. Regular check-ups with healthcare professionals and adherence to a well-rounded treatment plan can help manage these complications effectively, ensuring better overall health and well-being.

Treatment of Cystic fibrosis with other intestinal manifestations:

Treatment Options for Cystic Fibrosis with Other Intestinal Manifestations

Cystic fibrosis (CF) is a genetic disorder that primarily affects the lungs and digestive system. In some cases, individuals with CF may experience additional intestinal manifestations, which require specific treatment approaches. This article explores some of the treatment options available for managing cys...

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