International Journal of All Research Education & Scientific Methods

An ISO Certified Peer-Reviewed Journal

ISSN: 2455-6211

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Syringocystadenoma Papilliferum – A Rare Ca...

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Syringocystadenoma Papilliferum – A Rare Ca...

Syringocystadenoma Papilliferum – A Rare Case Report and Review of Literature

Author Name : Pal N., Uppender, P. Ahari

ABSRACT: Syringocystadenoma papilliferum (SCAP) is very rare skin adnexal tumour of apocrine gland origin located primarily on the scalp and appearing as a hairless nodular or plaque lesion. It is said to be common at birth or during puberty but cases in adults have also been reported. We have reported a case of scalp swelling in 22-year-young female. She was first clinically diagnosed with nevus sebaceous but later histopathologically confirmed to have syringocystadenoma papilliferum.