نتایج جستجو برای: syringocystadenoma papilliferum

تعداد نتایج: 216  

2017
Luanna da Silva Brito Léda Maria do Socorro Ventura Silva Lins Everson José dos Santos Leite Alberto Eduardo Cox Cardoso Ricardo Luis Simões Houly

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...

2015
Vani D

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...

Journal: :Northern International Medical College Journal 2015

2017
Luca Bruschini Annalisa Ciabotti Andrea De Vito Francesca Forli Christina Cambi Eugenio Maria Ciancia Stefano Berrettini

BACKGROUND Ceruminous glands are modified apocrine glands, situated in the external auditory canal, that, together with sebaceous glands, produce cerumen, better known as ear wax. The neoplastic transformation of these structures is very rare and there have been few cases reported in the literature. CASE REPORT Syringocystadenoma papilliferum is one of the rarest tumors among benign tumors aris...

2004
Alexander C. Katoulis Evangelia Bozi Nikolaos G. Stavrianeas

2009
Wei Liu Douglas R. Gnepp Egbert de Vries Haidy Bibawy Marshall Solomon Elizabeth S. Gloster

Sialadenoma papilliferum is a rare tumor, primarily of minor salivary gland origin, first described by Abrams and Finck (Cancer 24:1057-63, 1969). It is both an exophytic and endophytic papillary lesion histologically resembling syringocystadenoma papilliferum of sweat gland. The tumor is considered benign although rare recurrent cases have been reported. Three cases of malignant transformation...

Journal: :Dermatology online journal 2013
Johanna Peterson Kimberly Tefft Joseph Blackmon Anand Rajpara Garth Fraga

Syringocystadenocarcinoma papilliferum (SCACP) is a rare adenexal carcinoma with only 21 cases reported in the literature. Most patients describe a long-standing mass with recent change, supporting the idea that SCACP arises from malignant transformation of pre-existing syringocystadenoma papilliferum (SCAP). Syringocystadenocarcinoma papilliferum is generally treated with wide surgical excisio...

Akhtar Danish Fatima Talat Kumar Piyush Tiwary Anup Kumar

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...

Journal: :Annals of clinical and laboratory science 2002
Natalie Lama Monticciolo Jodie D Schmidt Michael B Morgan

Syringocystadenoma papilliferum (SP) commonly arises in conjunction with nevus sebaceous. Other less common lesions reported with SP include apocrine adenoma, condyloma acuminatum, hidradenoma papilliferum associated with hidrocystoma, poroma folliculare, and a single case ofverrucous carcinoma. We report the second case of verrucous carcinoma in conjunction with SP.

Journal: :QJM: An International Journal of Medicine 2018

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید