Syringocystadenoma papilliferum (deep seated horiostomatous): a case report

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...

Syringocystadenoma papilliferum Authors: Doctor

Giant naevoid syringocystadenoma papilliferum.

Sir, Syringocystadenoma papilliferum (SCAP) is a rare tumour first described in 1893 (1). To date, 400 cases have been reported worldwide. SCAP usually appears at birth or in early childhood, most frequently on the face or scalp. In approximately 25% of cases it is observed on other locations such as the trunk or the extremities. In 40% of cases, SCAP evolves contiguous to a pre-existing naevus...

Giant linear syringocystadenoma papilliferum on scalp.

minutes 00 seconds), clotting time (4 minutes 10 seconds), active partial thrombin time (27.4 seconds; normal range-24-32 seconds), prothrombin time, blood peripheral smear examination, liver function tests and renal function tests were all within normal limits. Urine and stool examination did not reveal erythrocytes or any abnormalities. Upper gastro-intestinal endoscopy and ultrasound of the ...

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...