نتایج جستجو برای: apocrine metaplasia

تعداد نتایج: 6237  

Journal: :Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2013
A Fernandez-Flores

Recently, it has been demonstrated how apocrine glands, as well as several cutaneous apocrine tumors, do not express calretinin. In the current report, we studied calretinin immunoexpression in 33 cases of cutaneous metastases of ductal breast carcinoma, as well as in seven primary cutaneous apocrine tumors. We also tested the hormonal status of all cases for estrogen receptors (ER), progestero...

Journal: :Anticancer research 2014
Manami Sasahara Akira Matsui Yoshiko Ichimura Yuuko Hirakata Yuuya Murata Eiji Marui

AIM Apocrine breast carcinoma often lacks estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor type-2 (HER2) expression. Accordingly, development of a new treatment strategy is important for this type of cancer. The growth stimulus through the androgen receptor (AR) can be a candidate for targeted treatment. Therefore, we examined the factors related t...

Journal: :The Journal of veterinary medical science 2012
Ayako Shiraki Yuri Hojo Takuma Tsuchiya Liyun Wang Takumi Ohishi Kazuhiko Suzuki Kunitoshi Mitsumori Makoto Shibutani

A rare case of complex apocrine carcinoma displaying dominant myoepithelial proliferation developed in the right leg subcutis of a 10-year-old male dog. The major cell population consisted of diffusely proliferating p63-expressing neoplastic cells that were largely myoepithelial in origin co-expressing α-smooth muscle actin. A small portion of the cell population consisted of concomitant basal ...

2013
Dong Xu Tienan Bi Huanrong Lan Wenjie Yu Wenmin Wang Feilin Cao Ketao Jin

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...

Journal: :Journal of Investigative Dermatology 1951

Journal: :Indian Journal of Dermatopathology and Diagnostic Dermatology 2015

Journal: :Annals of dermatology 2008
Seon-Wook Hwang Kyung-Jong Cho Doo-Jin Oh Deborah Lee Jung-Wook Kim Sung-Wook Park

A 28-year-old woman presented with multiple, asymptomatic, erythematous to bluish papules located on the chest. Histopathologically, three round, well defined cystic structures were seen on the upper and lower dermis. The first cyst was milia, the second was apocrine hidrocystoma and the other, largest cyst was an eruptive vellus hair cyst (EVHC). A diagnosis of multiple pilosebaceous cysts com...

2009
Marc Cohen David S. Cassarino Hubert B. Shih Elliot Abemayor Maie St. John

INTRODUCTION The classification of malignant sweat gland lesions is complex. Traditionally, cutaneous sweat gland tumors have been classified by either eccrine or apocrine features. METHODS A case report of a 33-year-old Hispanic man with a left scalp mass diagnosed as a malignancy of adnexal origin preoperatively is discussed. After presentation at our multidisciplinary tumor board, excision...

2013
Babita Kajal Hetal Talati Dean Daya Salem Alowami

Cutaneous vulvar carcinomas are predominantly of squamous cell carcinoma type. Primary vulvar adenocarcinomas are rare with a poorly understood histogenesis. They are classified into extramammary Paget's disease, sweat gland carcinomas, and breast-like adenocarcinomas of the vulva. Adenocarcinomas, originating from Bartholin glands, can also present as vulvar adenocarcinoma. Rare adenocarcinoma...

2011
T. Vasilakaki E. Skafida E. Moustou X. Grammatoglou E. Arkoumani K. Koulia A. Tsavari E. Delliou

Cutaneous apocrine gland carcinoma, a subtype of sweat gland carcinoma, is a very rare malignancy, and only few cases have been reported in the literature. Many of these carcinomas are indolent and slowly developing, but some are rapidly progressive. The treatment of choice is wide local excision with clear margins, with or without lymph node dissection. We report a case of a 67-year-old man wh...

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