[Skip to Content]
[Skip to Content Landing]
Article
January 1955

PRIMARY CUTANEOUS NORTH AMERICAN BLASTOMYCOSIS

Author Affiliations

Los Angeles; Charlottesville, Va.; Philadelphia; Memphis

From the University of Southern California, Department of Medicine—Dermatology and Syphilology—and the Los Angeles County General Hospital (Dr. Wilson); the Department of Dermatology, University of Virginia School of Medicine (Dr. Cawley), and the Department of Dermatology, University of Pennsylvania Medical School (Dr. Weidman). Dr. Gilmer is from the Department of Pathology, University of Tennessee School of Medicine.

AMA Arch Derm. 1955;71(1):39-45. doi:10.1001/archderm.1955.01540250041008
Abstract

DURING the half century following Gilchrist's delineation of North American blastomycosis as an entity in 1896, it became firmly established by many observers that the disease exists in two widely divergent forms. In one, the skin alone is apparently involved in a chronically progressive, ulcerative, granulomatous, and cicatrizing process, which usually persists over many years without affecting the general health of the patient. In the other, the lungs are the primary focus, from which the disease as a rule soon becomes widely disseminated, usually causing death. Rarely has a combination of these two forms, or a transition from one to the other, been observed. It has been widely accepted that this sharp differentiation occurs because of variation in the portal of entry of the infection, direct inoculation of the organisms into the skin causing the chronic cutaneous type, and inhalation into the lungs resulting in the

First Page Preview View Large
First page PDF preview
First page PDF preview
×