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  Vol. 117 No. 2, February 1969 TABLE OF CONTENTS
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Intestinal Lymphangiectasia

Metabolic Studies

Gholam-Hossein Amirhakimi, MD; I. Michael Samloff, MD; Michael F. Bryson, MD; Gilbert B. Forbes, MD

Am J Dis Child. 1969;117(2):178-185.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

INTESTINAL lymphangiectasia is associated with enteric loss of protein and malabsorption of fat.1-6 As a consequence, children with this disease fail to thrive,7,8 and display steatorrhea and hypoproteinemia with secondary edema of variable extent. Although the exact pathogenesis of this condition is as yet not completely understood, the response of a few patients with this syndrome to diet in which the fat is primarily medium-chain-triglycerides (MCT) has been remarkable.1,7-11 The purpose of this report is to present metabolic data obtained in a 15-year-old boy with isolated intestinal lymphangiectasia prior to and during MCT therapy.

Report of a Case

This white boy (SMH, 63-91-58), was the product of a normal full-term pregnancy. Delivery and neonatal period were uneventful. His growth, development, and general health were normal until age 4 years. At that time he underwent surgery for the repair of a right inguinal hernia. During the operation, milky . . . [Full Text PDF of this Article]


Author Affiliations

Rochester, NY

From the departments of pediatrics (Drs. Amirhakimi, Bryson, and Forbes) and medicine (Dr. Samloff), University of Rochester School of Medicine and Dentistry, Rochester, NY.


Footnotes

Received for publication Jan 26, 1968.

Reprint requests to 260 Crittenden Blvd, Rochester, NY 14620 (Dr. Forbes).



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