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  Vol. 17 No. 4, October 1967 TABLE OF CONTENTS
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Cephalic Mucormycosis (Phycomycosis)

A Case With Survival

Leon D. Prockop, MD; Margarita Silva-Hutner, PhD

Arch Neurol. 1967;17(4):379-386.

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

MUCORMYCOSIS, or phycomycosis, is a tissue infection by saprophytic fungi of the class Phycomycetes. It occurs in patients with debilitating diseases or following administration of adrenocorticosterioids, antitumor agents, or antibiotics. Patients with diabetic acidosis seem to be especially susceptible to mucormycosis.1 The common sites of initial invasion are the paranasal sinuses, lungs, or gastrointestinal tract.

Prior to 1943, 30 cases were collected from the literature, four involving the central nervous system.2 Since 1943, about 160 cases have been reported, 45 with cephalic involvement: paranasal sinus, orbit, cranial nerve, brain, or meninges.3-15 Death directly related to infection occurs in approximately 50% of all cases. To date only eight patients have survived cephalic infection, and all but one had residual neurological deficits (Table). The present report describes the ninth patient who has survived cephalic mucormycosis.

Report of a Case

This patient (P.H. 159-28-88) had recognized diabetes mellitus since . . . [Full Text PDF of this Article]


Author Affiliations

New York

From the Neurological Clinical Research Center, Department of Neurology, and the Mycology Laboratory, Department of Dermatology, College of Physicians and Surgeons, Columbia University and Columbia-Presbyterian Medical Center, New York.


Footnotes

Submitted for publication April 5, 1967; accepted April 21.

Reprint requests to Philadelphia General Hospital, Philadelphia 19104 (Dr. Prockop).



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