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Dyschondroplasia and Hemangiomata (Maffucci's Syndrome). II
WILLIAM BENNETT BEAN, M.D.
AMA Arch Intern Med. 1958;102(4):544-550.
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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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In 1955, I described two patients with Maffucci's syndrome and an infant with lesions suggesting the same diagnosis. I surveyed most of the cases reported up to that time since the classic modern description of the syndrome in 1942 by Carleton, Elkinton, Greenfield, and Robb-Smith. My purpose now is to record another case, report current observations on the two surviving patients described in 1955, discuss additional reports, some of which I overlooked in my earlier paper, and consider briefly some related syndromes. This rare disease is evoking much interest among internists, orthopedic surgeons and dermatologists.
It would appear that Maffucci's original paper has been inaccessible to most contemporary writers on this syndrome, and even his name is spelled with casual indifference. Recently I have obtained from what was the old Surgeon-General's Library a photostat of the original report by Angelo Maffucci from the Institute of Pathological Anatomy at the University
. . . [Full Text PDF of this Article]
Author Affiliations
Iowa City
From the Department of Internal Medicine and the University Hospitals of the College of Medicine of the State University of Iowa.
Footnotes
Submitted for publication Feb. 6, 1958.
Presented at the 5th International Congress of Internal Medicine, Philadelphia, April 24, 1958.
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