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HERMANN PINKUS, M.D.

AMA Arch Derm Syphilol. 1954;69(3):305-322.

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

IT IS THE purpose of this presentation to point out a sequence of events which appears to be typical in the development of naevus syringadenomatosus papilliferus, and by doing so to aid in the clinical recognition of this often unsuspected tumor. In addition, a clarification of some debated points in the histogenesis of naevus syringadenomatosus papilliferus will be attempted. The discussion will be restricted to those papilliferous growths which most commonly occur on or near the scalp and which develop in a preexisting lesion. Related tumors, particularly the papilliferous cystadenomas of the vulva, which Anderson¹ discussed before this Association three years ago, will not be considered.

Naevus syringadenomatosus papilliferus is judged a rare lesion by most authors. Biberstein (1926),² Reuterwall (1933),³ and Sachs and Lewis (1937)⁴ surveyed the older literature and collected approximately 40 cases. Probably an equal number has been added since that . . . [Full Text PDF of this Article]

Author Affiliations
MONROE, MICH.

From the Detroit Institute of Cancer Research; the Department of Dermatology, Wayne University College of Medicine, and the Department of Pathology, Wayne County General Hospital, Eloise, Mich.

Footnotes
Read at the Seventy-Third Annual Meeting of the American Dermatological Association, Lake Placid, N. Y., June 10, 1953.

Supported in part by grants to the Detroit Institute of Cancer Research from the American Cancer Society and the Kresge Foundation.

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