scholarly journals Polymorphous Adenocarcinoma of Lacrimal Gland: A Rare Case Report

2021 ◽  
Vol 8 (8) ◽  
pp. C115-119
Author(s):  
Md Ali Osama ◽  
Seema Rao ◽  
A K Grover
Keyword(s):  
Case Report ◽  
Lacrimal Gland ◽  
Malignant Neoplasm ◽  
Upper Lip ◽  
Polymorphous Adenocarcinoma ◽  
Common Location ◽  
Rare Case Report ◽  
Infiltrative Growth Pattern ◽  
Retromolar Region ◽  
Slow Growing

Polymorphous adenocarcinoma is a slow growing malignant tumor of minor salivary glands. The most common location of these tumors is palate, buccal mucosa, upper lip, floor of mouth and retromolar region. This malignant neoplasm is characterized by cytological uniformity, architectural diversity and infiltrative growth pattern. This is a case report of polymorphous adenocarcinoma occurring in lacrimal gland. They are seldom reported in this location and propose unique diagnostic challenges.

ANGIOLEIOMYOMA OF UPPER LIP: A RARE CASE REPORT

2017 ◽  
Vol 124 (2) ◽  
pp. e80
Author(s):  
LUIZ ARTHUR BARBOSA DA SILVA ◽  
EDUARDO ALONSO CRUZ MONROY ◽  
HUGO COSTA NETO ◽  
ANA MIRYAM COSTA DE MEDEIROS ◽  
PATRÍCIA TEIXEIRA DE OLIVEIRA ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Upper Lip ◽  
Rare Case Report

scholarly journals Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report

2014 ◽  
Vol 7 (1) ◽  
pp. 28-30
Author(s):  
Varsha Varshney ◽  
Gaurav Gupta ◽  
Mohnish Grover ◽  
Vikas Devra
Keyword(s):  
Case Report ◽  
Skull Base ◽  
Rare Case ◽  
Malignant Neoplasm ◽  
Complete Recovery ◽  
Burkitt’S Lymphoma ◽  
Anterior Skull Base ◽  
Burkitt's Lymphoma ◽  
Loss Of Vision ◽  
Rare Case Report

ABSTRACT Burkitt's lymphoma is a malignant neoplasm rarely found in paranasal sinuses and skull base. We report a rare case of Burkitt's lymphoma of anterior skull base associated with acute loss of vision. A 10 years old boy presented with history of headache, diminution of vision in right eye since 15 days. Biopsy showed diffuse NHL of Burkitt's type. After treatment with chemotherapy there was complete recovery in vision. How to cite this article Gupta G, Devra V, Grover M, Varshney V. Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report. Clin Rhinol An Int J 2014;7(1):28-30.

scholarly journals Retromastoid osteoma—a rare case report

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
Edmund Wooi Keat Tan ◽  
Jason Bae Barco ◽  
Mutee Ur Rehman ◽  
Choon Chieh Tan
Keyword(s):  
Case Report ◽  
Genetic Testing ◽  
Temporal Bone ◽  
Rare Case ◽  
Screening Colonoscopy ◽  
Adenomatous Polyposis ◽  
Rare Case Report ◽  
Computed Topography ◽  
The Right ◽  
Slow Growing

Abstract Osteomas are slow growing bone tumours and are often asymptomatic. Rarely, they can be present in the temporal bone—only few cases had been reported, with an incidence of 0.1–1%. We describe a case of an osteoma of the temporal bone (retromastoid) found in a 40 year old female, who presented with a slow growing swelling behind the right ear for 9 years. Diagnosis was made on non-contrast computed topography (CT) of the skull. Treatment is indicated in symptomatic cases or cosmetic reasons. Screening colonoscopy and genetic testing for familial adenomatous polyposis (FAP) and Gardner’s syndrome are advised.

scholarly journals Cytomorphological features of papillary cystadenocarcinoma of parotid gland: A case report with review of literature

CytoJournal ◽  
2016 ◽  
Vol 13 ◽  
pp. 12 ◽  
Author(s):  
Usha Joshi ◽  
Sanjay Singh Chufal ◽  
Naveen Thapliyal ◽  
Harsh Khetan
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Malignant Neoplasm ◽  
Separate Entity ◽  
Review Of Literature ◽  
Cystic Neoplasms ◽  
Cytological Features ◽  
Slow Growing ◽  
Nuclear Features

Papillary cystadenocarcinoma is a very rare slow growing malignant neoplasm characterized by cysts and intraluminal papillary projections. It is defined by WHO as a separate entity. On FNA, cytological features can mimic with various papillary and cystic neoplasms of salivary gland. It is also difficult to distinguish from benign salivary gland neoplasms as it has bland nuclear features. Thus we present cytomorphological features and discuss its differential diagnosis with neoplasms having prominent papillary architecture with review of literature.

scholarly journals Odontome presenting as fibrotic mass in the upper lip: A rare case report

2015 ◽  
Vol 5 (1) ◽  
pp. 38-40
Author(s):  
B Shrestha ◽  
K J Cho ◽  
J H Lee ◽  
S Subedi
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Female Patient ◽  
Rare Case ◽  
Developmental Stages ◽  
Upper Lip ◽  
Predisposing Factor ◽  
Early Developmental Stages ◽  
Rare Case Report ◽  
Early Developmental

The extraosseous occurrence of Odontome is rare. Trauma to the tooth bud during its early developmental stages has been proposed as a possible predisposing factor for the origin of odontome. In many cases etiology cannot be identified. Here we report an unusual and rare case of odontome presenting as a fibrotic mass on the upper lip in 32 years old female patient. The authors believe this is the rare documented case of odontome occurring within the soft tissue of upper lip.DOI: http://dx.doi.org/10.3126/jcmc.v5i1.12573

scholarly journals Pleomorphic adenoma of the upper lip: A rare case report

2020 ◽  
Vol 11 (2) ◽  
pp. 289
Author(s):  
AfakYusuf Sherwani ◽  
BaabarAli Shah ◽  
AmritPal Singh ◽  
SyedMasood Ahmad
Keyword(s):  
Case Report ◽  
Pleomorphic Adenoma ◽  
Rare Case ◽  
Upper Lip ◽  
Rare Case Report
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