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Intestinal lymphangiectasia--a case report.

C K Tan, K B Phua, G Chiang

Annals of the Academy of Medicine, Singapore

|October 1, 1983

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Primary intestinal lymphangiectasia, a rare cause of protein-losing enteropathy, was diagnosed in a young girl with generalized edema. This case highlights the importance of considering this condition in pediatric patients with similar symptoms.

Area of Science:

Gastroenterology
Pediatrics
Rare Diseases

Background:

Primary intestinal lymphangiectasia is an uncommon condition leading to protein-losing enteropathy.
It is characterized by the abnormal dilation of intestinal lymphatic vessels.

Observation:

A ten-month-old girl presented with generalized edema.
Diagnostic workup included an intestinal biopsy.

Findings:

The patient was diagnosed with primary intestinal lymphangiectasia.
Intestinal biopsy confirmed the diagnosis.

Implications:

This case underscores the need for timely diagnosis of rare pediatric gastrointestinal disorders.
Early identification and management of intestinal lymphangiectasia are crucial for improving patient outcomes.

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