Intestinal lymphangiectasia is a very rare disease whereby small lymphatic vessels in the intestines swell up and lose their contents into the gut containing protein and fat. In the long run, the leakage may cause a phenomenon known as swelling (edema), inefficient absorption of nutrients, and a more severe chance of attracting infection.
Patients with intestinal lymphangiectasia may experience:
This condition can arise in two main forms:
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The coding is also referred to as ICD-10 (K90.8), which is applied to other forms of malabsorption as well.
Yes. The protein amount in the blood can be decreased, and this raises the chances of forming blood clots.
It is diagnosed by means of imaging scans, blood tests, and endoscopic examination of the intestines.
The biopsy samples, as a rule, indicate the appearance of enlarged lymphatic vessels and fats in the intestinal lining.
Your care should be handled by a gastroenterologist who has experience with rare lymphatic and digestive disorders.
Yes. An expert low-fat, high-protein diet containing medium-chain triglyceride (MCT) oils can help alleviate symptoms and reduce exacerbations.
Surgical intervention is not very common but can be considered in cases of established lymphatic obstruction.
Usually, a follow-up visit is planned every 3 to 6 months, depending on your symptoms and laboratory test results.
Yes. Primary intestinal lymphangiectasia may manifest in children or young infants.
Most people live normal lives with proper management, regular monitoring, and dietary control, which help manage symptoms effectively.