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  Vol. 104 No. 5, November 1971 TABLE OF CONTENTS
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Multiple Congenital Giant Nevocellular Nevi With Halos

A Clinical and Electron Microscopic Study

Richard S. Berger, MD; John J. Voorhees, MD

Arch Dermatol. 1971;104(5):515-521.


Abstract

A patient had multiple congenital giant nevocellular nevi all of which had halos but none of which regressed. This unusual phenomenon was studied histochemically and ultrastructurally in an attempt to compare this process with ordinary halo nevi and other known leukodermatous disorders. Histochemical studies demonstrated a decrease in melanin and tyrosinase activity in the area of the halo. Although the relative frequency of clear cells in the halo remained normal, electron microscopy revealed an increased density of Langerhans cells in the hypochromic zone and a variable deficit in the number of melanocytes. Ultrastructurally these melanocytes were markedly deficient in melanized melanosomes. These results suggest that either we may be dealing with an unusual form of leukoderma acquisitum centrifugum or a variant of one of the other congenital leukodermatous diseases.



Author Affiliations

Ann Arbor, Mich

From the Department of Dermatology, University of Michigan Medical School, Ann Arbor. Dr. Berger is now with the University of Missouri School of Medicine, Columbia.


Footnotes

Accepted for publication April 16, 1971.

Reprint requests to Division of Dermatology, University Hospital, Columbia, Mo 65201 (Dr. Berger).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Halo Congenital Nevus Undergoing Spontaneous Regression: Involvement of T-Cell Immunity in Involution and Presence of Circulating Anti--Nevus Cell IgM Antibodies
Tokura et al.
Arch Dermatol 1994;130:1036-1041.
ABSTRACT  

Halo Congenital Nevus
Brownstein et al.
Arch Dermatol 1977;113:1572-1575.
ABSTRACT  





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