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  Vol. 88 No. 5, November 1963 TABLE OF CONTENTS
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Pathergic Granulomatosis

Disseminated Type With Ulceronodular Dermatitis and Leukopenia: Report of Two Cases

GEORGE W. BINKLEY, MD

Arch Dermatol. 1963;88(5):637-643.

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

Pathergy has been defined as the totality of the morbid phenomena which can be produced by a state of altered reactivity.

The related chronic necrotizing diseases of single or multiple organs have posed many problems. Of these problems, the most difficult are the nomenclature, the causation, and the therapy. The variations in the patterns of pathergic granulomatosis are legion. One of the earliest of these illnesses to be described was lethal midline granulomatosis.1 Soon after came dermatitis nodularis necrotica.2-4 Dermatitis nodularis necrotica presents distinctive clinical features which, at first, forced one to regard it as unrelated to midline granuloma and other chronic dermonecrotic diseases; now I consider it a pathergic disease. Polyarteritis nodosa5 belongs here, as does Wegener's granulomatosis6 (pathergic granulomatosis7) with all its designations and eponyms. Laymon8 brought malignant papulosis with atrophy into this group. Winkelmann9 and others10 have reviewed the . . . [Full Text PDF of this Article]


Author Affiliations

CLEVELAND

Assistant Clinical Professor of Medicine (Dermatology), Western Reserve University.


Footnotes

Presented at the 83rd Annual Meeting of the American Dermatological Association, Inc., April 16-19, 1963.

Supported in part by grants from the Department of Health, Education and Welfare and Armed Forces Epidemiology Board.



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