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Case Studies | Pathology | India | Volume 4 Issue 10, October 2015

Syringocystadenoma Papilliferum - A Case Report

Dr. Kamakshi Worah | Dr. D.B. Borkar | Dr. Reeta Dhar ^[5] | Dr. Shilpi Sahu ^[3] | Dr. Prabhakar Patro

Abstract: Syringocystadenoma papilliferum exceedingly rare skin adnexal neoplasm of apocrine gland origin located primarily on the scalp and appearing as a hairless nodular /plaque lesion. In one third of the cases Syringocystadenoma papilliferum is associated with Naves Sebaceous of Jadassohn. A strong clinical acumen, prompt excision and confirmation by histopathology underline treatment of this deceptively docile neoplasm. We report a case of 9 year old boy because of its rarity and tendency for vagrant behavior.

Keywords: Syringocystadenoma papilliferum, Naves sebaceous of Jadassohn, Apocrine gland origin, Plaque, Vagrant behaviour

Edition: Volume 4 Issue 10, October 2015,

Pages: 2229 - 2231