نتایج جستجو برای: salivary duct carcinoma

تعداد نتایج: 444154  

Journal: :Head & neck 2016
Sarina Müller Konstantinos Mantsopoulos Heinrich Iro Abbas Agaimy

BACKGROUND Salivary duct carcinoma is a rare, aggressive tumor entity first described by Kleinsasser et al in 1968, as a group of malignant salivary gland tumors characterized by duct formation and central necrosis. A case with an unusual localization in the nasal cavity and maxillary sinus is being described in our report. METHODS A 60-year-old patient presented with difficulty of nasal brea...

2017
Wahida Chakari Luise Andersen Jørgen Lock Andersen

Salivary duct carcinoma is a rare and highly aggressive malignant neoplasm that frequently metastasises to other organs, but cutaneous metastasis is uncommon. There are only 6 cases reported in the literature with metastases to the skin and in all cases the tumour originates from the parotid gland. We present a case of skin metastases from the submandibular gland that was mistaken for basal cel...

2016
Chetana Chandrasekar Naser Salati Lakshmi Rao Raghu Radhakrishnan

Salivary duct carcinoma (SDC) is a high-grade adenocarcinoma arising from the ductal epithelium of salivary glands which rarely involves the minor salivary glands. The varied histological presentation in the minor salivary gland tumors makes them the most heterogeneous group of neoplasms, making the diagnosis a challenge. This report highlights the importance of immunohistochemical markers in t...

Journal: :Head & neck 2016
Meredith L Johnston Shao Hui Huang John N Waldron Eshetu G Atenafu Kelvin Chan Bernard J Cummings Ralph W Gilbert David Goldstein Patrick J Gullane Jonathan C Irish Bayardo Perez-Ordonez Ilan Weinreb Andrew Bayley John Cho Laura A Dawson Andrew Hope Jolie Ringash Ian J Witterick Brian O'Sullivan John Kim

BACKGROUND Salivary duct carcinoma is rare, with distinct morphology and behavior. We reviewed our institutional experience with salivary duct carcinoma, aiming to characterize clinical behavior and treatment outcomes. METHODS All salivary duct carcinomas treated curatively between 1999 and 2010 were reviewed. Overall survival (OS), locoregional control, distant control, and patterns of failu...

2016
Pavel Dulguerov Giulio Cantu Chandra L Pandey

Salivary duct carcinoma is a distinctive primary neoplasm of the major salivary gland characterized by aggressive behavior with early metastasis, local recurrence and significant mortality. We report a 40 year old male with parotid swelling diagnosed as pleomorphic adenoma, who underwent parotidectomy with modified radical neck dissection and later, on routine histopathology, the swelling was r...

Journal: :Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2014
Gamze Atay Cavid Cabbarzade Gökhan Gedikoğlu Ali Şefik Hoşal

Hybrid carcinomas are rare neoplasms which are characterized by two different types of tumors localized in a single topographic region of the lesion. Parotid gland is the most common involvement site of hybrid carcinomas among salivary glands. The aggressiveness of the hybrid tumor depends on its high-grade component. In this article, we present a 71-year-old male case with the left parotid gla...

Journal: :Head and neck pathology 2013
Susan Müller Lester D R Thompson

Over the past few decades, salivary gland tumor pathology has evolved. This includes recognition of newly defined entities as well as reclassification of other salivary gland tumors [1]. The development of genetic tests have shown that some salivary gland tumors have genetic abnormalities which are specific to a histologic type such as MECT1– MAML2 gene fusion in mucoepidermoid carcinoma and PL...

Journal: :European Annals of Otorhinolaryngology, Head and Neck Diseases 2011

Journal: :Practica Oto-Rhino-Laryngologica 1994

Journal: :Histopathology 2007
S Meer M Altini

AIMS To evaluate cytokeratin (CK) 7/20 expression patterns in salivary gland neoplasia. METHODS AND RESULTS Formalin-fixed paraffin embedded tissue from 153 salivary gland tumours were evaluated for CK7/20 immunoreactivity. The tumours included pleomorphic adenoma (n = 24), myoepithelioma (n = 9), papillary cystadenoma (n = 3), oncocytoma (n = 2), adenoid cystic carcinoma (n = 22), mucoepider...

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