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  Vol. 9 No. 2, February 1924 TABLE OF CONTENTS
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A CASE OF DIFFUSE SCLERODERMA PRESENTING UNUSUAL FEATURES

CHARLES MALLORY WILLIAMS, M.D.

Arch Derm Syphilol. 1924;9(2):187-207.

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 etiology and pathogenesis of the so-called idiopathic scleroses and atrophies of the skin is still such a mystery, and the classification is in many ways so unsatisfactory, that the record of a case which presents such a variety of symptoms as occurred in the patient about to be described may be of interest and perhaps of value.

REPORT OF A CASE

History.—

E. G., an American girl, aged 12, was admitted to the New York Skin and Cancer Hospital on Oct. 26, 1922, with a diagnosis of scleroderma. The family history was negative for tuberculosis and syphilis. The patient had had scarlet fever when about 4 years of age, with uneventful recovery, and measles in May, 1918, when about 71/2 years old. Soon after recovery from measles, the patient said, she had a sore mouth, involving the buccal and labial mucous membrane, and lasting about two weeks. This seems . . . [Full Text PDF of this Article]


Author Affiliations

Professor of Dermatology, University of Vermont; Attending Physician, New York Skin and Cancer Hospital NEW YORK



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