Results 11 to 20 of about 44,493 (220)

Polymorphous adenocarcinoma of the parotid – An uncommon site of occurrence

open access: yesInternational Journal of Advanced Medical and Health Research, 2022
Polymorphous low-grade adenocarcinoma is a neoplasm of the minor salivary glands and is malignant in origin but is indolent in nature. Currently, this neoplasm is documented and known as polymorphous adenocarcinoma (PAC) by WHO Classification of Salivary
Prabhat Mahato   +3 more
doaj   +1 more source

Giant pleomorphic adenoma in the parapharyngeal space

open access: yesRevista Portuguesa Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, 2013
Parapharyngeal tumours are rare. Usually they are asymptomatic but by growing they can reach compressive clinic and displacement of adjacent structures, as the case presented, with 8 cm of diameter. They are usually benign.
M Padilla Parrado   +5 more
doaj   +1 more source

An extremely rare case of giant oncocytic adenolipoma of the parotid gland

open access: yesClinical Case Reports, 2020
Oncocytic adenolipoma is a rare tumor to occur in the salivary gland, which can present as a giant neck mass. Until now,
Dipesh Shakya, Ajit Nepal
doaj   +1 more source

Rare parotid tumor. A case report and literature review [PDF]

open access: yesBatna Journal of Medical Sciences
Salivary lymphoepithelial carcinoma is a rare tumour characterized by non- neoplastic lymphocyte infiltration associated with epithelial proliferation. This is primarily the parotid gland.
Mohamed HACHEMI   +4 more
doaj   +1 more source

Cytomorphological findings and histological correlation of papillary cystadenocarcinoma of the parotid: Not always a low-grade tumor

open access: yesIndian Journal of Pathology and Microbiology, 2016
Papillary cystadenocarcinoma (PCAC) is a rare salivary gland tumor characterized by a predominantly cystic growth that often exhibits intraluminal papillary growth without specific histologic features of other cystic salivary gland tumors.
Yasmeen Khatib   +3 more
doaj   +1 more source

Parotid angiofibroma

open access: yesJournal of Oral and Maxillofacial Pathology, 2014
Angiofibromas are rare, benign, locally invasive vascular tumors, which represent 0.05-0.5% of all head and neck tumors. Most frequent site of occurrence is the posterior nasopharynx, called as nasopharyngeal angiofibromas (NA), when these arise outside the nasopharyngeal region they are termed as extranasopharyngeal angiofibromas (ENA).
Hallur, Neelakamal H   +3 more
openaire   +3 more sources

Pembrolizumab in a Patient With a Metastatic CASTLE Tumor of the Parotid

open access: yesFrontiers in Oncology, 2019
Carcinoma showing thymus-like elements (CASTLE) is a rare tumor, most commonly found in the thyroid gland. Here we report a case of CASTLE tumor localized to the parotid gland, recognized in retrospect after a late manifestation of symptomatic pleural ...
Lisa Lorenz   +7 more
doaj   +1 more source

Launay’s External Carotid Vein

open access: yesMedicina, 2021
Background and Objectives: Launay’s external carotid vein (ECV) is poorly represented in the anatomical literature, although it is an occasional satellite of the external carotid artery (ECA). We aimed to establish the incidence and morphology of the ECV.
Mihaela Daniela Manta   +3 more
doaj   +1 more source

Facial nerve palsy following parotid gland surgery: A machine learning prediction outcome approach

open access: yesWorld Journal of Otorhinolaryngology-Head and Neck Surgery, 2023
Introduction Machine learning (ML)‐based facial nerve injury (FNI) forecasting grounded on multicentric data has not been released up to now. Three distinct ML models, random forest (RF), K‐nearest neighbor, and artificial neural network (ANN), for the ...
Carlos M. Chiesa‐Estomba   +9 more
doaj   +1 more source

Actinomycosis of the parotid masquerading as malignant neoplasm.

open access: yesBMC Cancer, 2004
Background Primary actinomycosis of the parotid gland is of rare occurrence and can mimic a malignant neoplasm both clinically as well as radiologically.
Ramachandran K   +3 more
doaj   +1 more source

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