A case of syringocystadenoma papilliferum of eyelid with literature review

Syringocystadenoma papilliferum of eyelid A deviant case report

Syringocystadenoma papilliferum, a distinct dermatologic entity, is an exceedingly rare benign skin neoplasm and seems to have arisen from apocrine or eccrine adnexal structures. The diagnosis is clinically suspected and histologically confirmed due to its non presentations. Since it usually appears at birth or during puberty and adolescence, Childhood tumor. Complete surgical excision is the t...

A case series of three atypical cases of syringocystadenoma papilliferum with thigh, abdomen and axillary involvement, and review of literature

Syringocystadenoma papilliferum is an uncommon benign apocrine gland tumour, mostly of congenital or early childhood onset, affecting head and neck. In addition, nevus sebaceous is commonly associated with this tumor. Here, we document three cases of syringocystadenoma papilliferum with many atypical features, such as the involvement of rare sites (abdomen, axilla and thigh), absence of nevus s...

Dermoscopy of a rare case of linear syringocystadenoma papilliferum with review of the literature

Syringocystadenoma papilliferum (SCAP) is a benign hamartomatous tumor arising from pluripotent cells with either apocrine or eccrine differentiation. We report a rare case of de novo linear SCAP in a 12-year-old female child with lesions over the chest along with the dermoscopic findings.

Syringocystadenoma papilliferum in the right lower abdomen: a case report and review of literature

Syringocystadenoma papilliferum (SCAP) is an uncommon benign adnexal tumor of the skin. It is frequently seen in association with other benign adnexal lesions, such as nevus sebaceous, apocrine nevus, tubular apocrine adenoma, apocrine hidrocystoma, apocrine cystadenoma, and clear cell syringoma. The unusual reported locations of SCAP include the head and neck, the buttock, the vulva, the scrot...

Syringocystadenoma papilliferum Authors: Doctor