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  Vol. 65 No. 2, February 1952 TABLE OF CONTENTS
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ANGIOSARCOMA IN POSTMASTECTOMY LYMPHEDEMA (STEWART-TREVES SYNDROME)

MAX JESSNER, M.D.; FREDERICK G. ZAK; CHARLES R. REIN, M.D.

AMA Arch Derm Syphilol. 1952;65(2):123-129.

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

The SYNDROME characterized by the appearance of cutaneous lymphangiosarcoma in the ipsilateral arm, years after radical mastectomy for carcinoma, has been described by Stewart and Treves.1 We had occasion to see a patient with this until recently unknown disorder.

REPORT OF A CASE

A. N., a 54-year-old, white, single woman, a patient of Dr. H. Wadro, had a radical mastectomy in 1942 for carcinoma of the left breast, with axillary node involvement, followed by extensive x-ray treatment and, several months later, by radium therapy to the axilla.

Edema of the left arm developed shortly after the operation but regressed to about 50% in recent years. It was most conspicuous above the left elbow, where the arm measured 111/2 in. (29 cm.) as compared with 8 in. (20.3 cm.) above the right elbow.

In April, 1949, the patient noticed bluish, firm, raised nodules on the inner aspect of . . . [Full Text PDF of this Article]


Author Affiliations

NEW YORK

From the Department of Dermatology and Syphilology of the Post-Graduate Medical School of New York University-Bellevue Medical Center (Dr. Marion B. Sulzberger, Chairman), and New York Skin and Cancer Hospital.


Footnotes

Presented at the Seventy-first Annual Meeting of the American Dermatological Association, May 26, 1951, Hot Springs, Va.



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