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Case Studies | Pathology | Volume 4 Issue 10, October 2015 | Pages: 2229 - 2231 | India
Syringocystadenoma Papilliferum - A Case Report
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
How to Cite?: Dr. Kamakshi Worah, Dr. D.B. Borkar, Dr. Reeta Dhar, Dr. Shilpi Sahu, Dr. Prabhakar Patro, "Syringocystadenoma Papilliferum - A Case Report", Volume 4 Issue 10, October 2015, International Journal of Science and Research (IJSR), Pages: 2229-2231, https://www.ijsr.net/getabstract.php?paperid=SUB159148, DOI: https://dx.doi.org/10.21275/SUB159148