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  Vol. 82 No. 5, November 1960 TABLE OF CONTENTS
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Angiokeratoma Corporis Diffusum

MAJOR WILLIAM R. VINEYARD, MC; CAPT. EDWARD J. KAMIN, MC

Arch Dermatol. 1960;82(5):817-819.

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

In 1898, Fabry1 reported a previously undescribed cutaneous disorder which has since been termed angiokeratoma corporis diffusum. Over the next few decades, dermatological periodicals contained reports of other examples of this condition. It slowly became apparent that this disorder was not limited to the integument, and that the cutaneous lesions merely represent the earliest and most easily demonstrable evidence of a sometimes fatal syndrome involving multiple organs.2,3 We wish to report an additional case of this syndrome and briefly review the characteristic manifestations.

The cutaneous lesions are the earliest aberration and have been present in all reported cases. They consist of minute macules and papules which may or may not have an overlying scale. The lesions are dark blue-red to purple in color and may appear black in older individuals. Slight, if any, change on diascopic pressure is characteristic. They are scattered over the entire body but tend . . . [Full Text PDF of this Article]


Author Affiliations

USA; USA

Dermatology Service (Major Vineyard) and Department of Medicine (Captain Kamin), Walter Reed General Hospital, Washington, D.C.


Footnotes

Submitted for publication March 21, 1960.



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