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  Vol. 127 No. 7, July 1991 TABLE OF CONTENTS
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Congenital Basal Cell Carcinoma

Patricia A. Ledwig, MD; Amy S. Paller, MD
Division of Dermatology The Children's Memorial Hospital 107 2300 Children's Plaza Chicago, IL 60614

Arch Dermatol. 1991;127(7):1066-1067.

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

To the Editor.—

Basal cell carcinoma (BCC) is an uncommon skin tumor in prepubertal children, and is usually associated with basal cell nevus syndrome, Bazex syndrome, or xeroderma pigmentosum. Basal cell tumors that develop within a nevus sebaceous rarely appear before puberty.1 We report a biopsy-proven BCC that occurred in an otherwise healthy 6-year-old white boy; the lesion was initially noticed at birth as a small skin-colored papule at the left supraclavicular area. The lesion remained relatively unchanged and was excised 6 years later at the mother's request. Basal cell carcinoma was not suspected clinically. Histologic sections revealed solid masses and strands of basaloid cells, several areas of which formed glandlike structures (Figure). The lumina were filled with amorphous, somewhat eosinophilic material. There was also a mild fibrous reaction of the stroma, vascular dilatation, and scattered perivascular infiltrates in the dermis. There was no evidence of associated nevus . . . [Full Text PDF of this Article]



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