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
Neurilemmoma is usually a solitary nerve sheath tumor, most often seen in adults. Tl: neurilemmomas of the oral cavity have been reported to develop on the tongue, buccal m7; Cosa, palate, gingiva, floor of the mouth, and lower lip, in order of frequency. We describe 7-year-old boy witlf an asymptomatic, solitary neurilemmoma on his upper lip with a brit: review of the literature. Neurilemmoma should be considered as one of the tumors that ca develop on children's lips.
Subject(s)
Adult , Child , Humans , Male , Gingiva , Lip , Mouth , Neurilemmoma , Palate , TongueABSTRACT
Juvenile cellular adenofibroma of the breast is a unique neoplasm of the breast that should be differentiated from other important benign and malignant lesions of the juvenile breasts. We report a case with it's characteristic clinical, gross and histological features. The tumor was in the right breast with the size of 20 cm in maximum extent. This patient was also associated with hemihypertrophy of the right side. Microscopically the masses were characterized by prominent stromal cellularity associated with pericanalicular duct proliferation.