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INTESTINAL LIPODYSTROPHY (WHIPPLE'S DISEASE)
LOUIS T. PALUMBO, M.D.;
GEORGE M. RUGTIV, M.D.
AMA Arch Surg. 1951;62(4):604-608.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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THE RARE occurrence and infrequent recognition of intestinal lipodystrophy as described by Whipple1 in 1907 appears to warrant report of a case diagnosed recently during laparotomy. The case reported by Whipple was characterized anatomically by deposits of fat and fatty acids in the intestinal and mesenteric lymphatic tissues. Clinically, the patient had recurring attacks of arthritis, emaciation. enlargement and tenderness of the abdomen and fatty diarrhea.
Since the original description of this disease, few reports have appeared in the literature.2 To date the total number represents about 24 cases. The last case appeared in the literature in 1949, as reported by Copland and others.2b Several other authors have used the following terminology for this entity: lipophagia granulomatosis, lymphadenocele, mesenteric chyle adenectasis and lymphadenectasis.
REPORT OF A CASE
A 53 year old white man was admitted to the hospital in January 1950 with the complaint of dull aching
. . . [Full Text PDF of this Article]
Author Affiliations
DES MOINES, IOWA
From the departments of surgery (Dr. Palumbo) and pathology (Dr. Rugtiv), Veterans Administration Hospital.
Footnotes
Sponsored by the Veterans Administration and published with the approval of the Chief Medical Director. The statements and conclusions published by the authors are the results of their own study and do not necessarily reflect the opinion or policy of the Veterans Administration.
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