ABSTRACT
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 distinct clinical findings and varried presentations. Since it usually appears at birth or during puberty and adolescence, it is called as Childhood tumor. Complete surgical excision is the treatment of choice followed by detailed histologic examination, to avoid the risk of maligrant degeneration. Herein, We have reported a rare case of Syringocystadenoma papilliferum of eyelid in an adolescent female.
ABSTRACT
Liposarcoma of the paratesticular region is a rare malignant soft tissue neoplasm. Out of all the possible sites of liposarcoma, the incidence in spermatic cord is rare, accounting for only 5% of these neoplasms. Among the various subtypes of liposarcoma described in the paratesticular region, myxoid variant of liposarcoma is seen very rarely. One such case is we ported here for its rarity and also to draw attention to the fact that, early diagnosis and complete excision carry better prognostic value.