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  Vol. 123 No. 4, April 1987 TABLE OF CONTENTS
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Familial Occurrence of Lichen Sclerosus et Atrophicus

Case Reports of a Mother and Daughter

Joseph A. Shirer, Jr, MD; Marilyn C. Ray, MD

Arch Dermatol. 1987;123(4):485-488.


Abstract



• A mother and daughter with lichen sclerosus et atrophicus (LSA) are described. Both had lesions restricted to their lower legs. Both patients were positive for HLA-B40, which has been associated with LSA. Sex steroid hormones showed no decrease in dihydrotestosterone, free testosterone, or androstenedione levels in the daughter as was demonstrated in a previous study of this disease, but did show some decrease in androstenedione in the mother. This article provides further evidence for a possible familial predisposition for LSA.

(Arch Dermatol 1987;123:485-488)



Author Affiliations



From the Department of Dermatology, Ochsner Clinic and Alton Ochsner Medical Foundation (Drs Shirer and Ray), and the Department of Dermatology, Louisiana State University (Dr Shirer), New Orleans.


Footnotes



Accepted for publication Sept 3, 1986.

Reprint requests to Ochsner Clinic, 1514 Jefferson Hwy, New Orleans, LA 70121 (Dr Ray).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Hypopigmented, Hyperkeratotic Macules in a Teenager
Petersen et al.
Arch Dermatol 1997;133:651-652.
ABSTRACT  

HLA Antigens in Lichen Sclerosus et Atrophicus
Purcell et al.
Arch Dermatol 1990;126:1043-1045.
ABSTRACT  





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