1998Archives of Disease in ChildhoodOpen access

Intestinal lymphangiectasia and protein losing enteropathy responding to small bowel resection

Mladen Peršić, N L Browse, Igor Prpić

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Abstract

Editor,—Primary intestinal lymphatic obstruction with protein losing enteropathy (PLE) may be associated with other lymphatic drainage abnormalities outside the gastrointestinal tract. The pathogenesis, classification, management, and prognosis of these conditions continues to be discussed.1 2 We present a patient with PLE whose disorder has been followed up for nearly 20 years. The patient, was aged 13 months when he originally presented to the Paediatric University Hospital Centre in Rijeka, Croatia with watery diarrhoea and generalised oedema. The laboratory features, including a low serum total protein and albumin, were consistent with PLE. He was treated with a high protein and low fat diet supplemented with medium chain triglycerides. After initial improvement …

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Editor,—Primary intestinal lymphatic obstruction with protein losing enteropathy (PLE) may be associated with other lymphatic drainage abnormalities outside the gastrointestinal tract. The pathogenesis, classification, management, and prognosis of these conditions continues to be discussed.1 2 We present a patient with PLE whose disorder has been followed up for nearly 20 years. The patient, was aged 13 months when he originally presented to the Paediatric University Hospital Centre in Rijeka, Croatia with watery diarrhoea and generalised oedema. The laboratory features, including a low serum total protein and albumin, were consistent with PLE. He was treated with a high protein and low fat diet supplemented with medium chain triglycerides. After initial improvement …

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Available abstract

Editor,—Primary intestinal lymphatic obstruction with protein losing enteropathy (PLE) may be associated with other lymphatic drainage abnormalities outside the gastrointestinal tract. The pathogenesis, classification, management, and prognosis of these conditions continues to be discussed.1 2 We present a patient with PLE whose disorder has been followed up for nearly 20 years. The patient, was aged 13 months when he originally presented to the Paediatric University Hospital Centre in Rijeka, Croatia with watery diarrhoea and generalised oedema. The laboratory features, including a low serum total protein and albumin, were consistent with PLE. He was treated with a high protein and low fat diet supplemented with medium chain triglycerides. After initial improvement …

Key concepts: Protein losing enteropathy, Medicine, Enteropathy, Lymphatic system, Lymphangiectasia, Gastroenterology, Internal medicine, Gastrointestinal tract

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