Giant naevoid syringocystadenoma papilliferum.

A Case of Giant Squamous Cell Carcinoma of the Buttock Possibly Arose from Syringocystadenoma and Invaded to the Rectum

We report a rare case of giant squamous cell carcinoma of the buttock infiltrated to the rectum. The tumor may have arisen from syringocystadenoma papilliferum. Since there was no sign of metastasis, radical operation including rectal amputation was performed after successful neoadjuvant therapies. Afterwards, the patient has been alive free from disease for 15 months with no lymph node and dis...

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 combined with a tubular apocrine adenoma*

Syringocystadenoma papilliferum and tubular apocrine adenoma are rare benign sweat gland tumors. Syringocystadenoma papilliferum occurs alone or in association with other tumors. Although it is rare, the association of tubular apocrine adenoma with syringocystadenoma papilliferum developing in a sebaceous nevus on the scalp is well documented. However, the co-existence of these two tumors witho...

Syringocystadenoma papilliferum Authors: Doctor

Giant condyloma acuminata with syringocystadenoma papilliferum.

350 six months. The same lesion had gradually increased to attain the present size. Family and personal history were not contributory. Dermatological examination revealed two skin lesions on the medial aspect of the right thigh [Figure 1]. The larger one was 6 × 7 cm in size and smaller one was 1 × 3 cm in size. Both were firm in consistency, non-tender, mobile on the underlying structure, caul...