scholarly journals A rare case of Ewing sarcoma metastasis to the oral cavity

2021 ◽  
Vol 51 ◽  
Author(s):  
Riéli Elis Schulz ◽  
Matheus Henrique Alves de Lima ◽  
Rodrigo Nascimento Lopes ◽  
Clovis Antonio Lopes Pinto ◽  
Ulisses Ribaldo Nicolau ◽  
...  
Keyword(s):  
Oral Cavity ◽  
Ewing Sarcoma ◽  
Rare Case ◽  
Sarcoma Metastasis

Chronic intermittent torticollis in a toddler: a rare case of axis (C2) Ewing sarcoma presentation

2017 ◽  
Author(s):  
Vassilios Papadakis ◽  
Elpis Vlachopapadopoulou ◽  
Kondylia Antoniadi ◽  
Vassiliki Tzotzola ◽  
John Nikas ◽  
...  
Keyword(s):  
Ewing Sarcoma ◽  
Rare Case

scholarly journals Metastasis of Ewing Sarcoma to the Pancreas: Case Report and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Hyma Polimera ◽  
Prashanth Moku ◽  
Shady Piedra Abusharar ◽  
Monali Vasekar ◽  
Jayakrishna Chintanaboina
Keyword(s):  
Ewing Sarcoma ◽  
Rare Case ◽  
Bone Cancer ◽  
Positive Outcome ◽  
Tumor Burden ◽  
Response To Treatment ◽  
Effective Management ◽  
Review Of The Literature ◽  
Appropriate Treatment ◽  
Prompt Diagnosis

Ewing sarcoma (ES) is a highly aggressive malignant bone cancer. ES is part of the Ewing sarcoma family of tumors (ESFT), which express characteristic t(11;22) translocation as well as higher levels of CD99. Given that metastasis and tumor burden are significant prognostic factors in patient’s response to treatment, prompt diagnosis is needed to effectively treat ESFT patients. However, the challenges in classifying and characterizing ESFT complicate effective management and treatment of ES. In this report, we present a rare case of ES metastasis to the pancreas. Upon review of the literature, we found 39 cases of ESFT involving the pancreas, but only 3 were metastatic to the pancreas while the remaining cases of ESFT primarily originated from the pancreas. Given the rarity of such metastasis, the positive outcome in our patient’s case may explain the importance of prompt diagnosis in order to initiate appropriate treatment.

Accessory oral cavity associated with duplication of the tongue and the mandible in a newborn: A rare case of Diprosopus. Multi-row detector computed tomography diagnostic role

2014 ◽  
Vol 42 (8) ◽  
pp. 1924-1928 ◽  
Author(s):  
Rosa Morabito ◽  
Michele R. Colonna ◽  
Enricomaria Mormina ◽  
Ferdinando Stagno d'Alcontres ◽  
Vincenzo Salpietro ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Oral Cavity ◽  
Rare Case ◽  
Diagnostic Role

scholarly journals Nevus of Ota with Rare Palatal Involvement: A Case Report with Emphasis on Differential Diagnosis

2011 ◽  
Vol 2011 ◽  
pp. 1-4
Author(s):  
Gaurav Sharma ◽  
Archna Nagpal
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Oral Cavity ◽  
Rare Case ◽  
Indian Subcontinent ◽  
English Literature ◽  
Melanocytic Nevus ◽  
Oral Manifestations ◽  
Nevus Of Ota ◽  
The Face

Nevus of Ota, a dermal melanocytic nevus, is rare in the Indian subcontinent. It presents as a brown, blue, or gray patch on the face and is within the distribution of the ophthalmic and maxillary branches of the trigeminal nerve. The oral cavity is infrequently involved in nevus of Ota. Only 11 cases have been documented in the English literature. We report a rare case of intraoral nevus of Ota in a 22-year-old male patient. This paper focuses on the differential diagnosis of oral manifestations of nevus of Ota to assist in proper followup to avert malignant transformation.

scholarly journals Glomus Tumor of the Oral Cavity: Report of a Rare Case and Literature Review

2019 ◽  
Vol 30 (2) ◽  
pp. 185-190 ◽  
Author(s):  
Celeste Sánchez-Romero ◽  
Maria Eduarda Pérez de Oliveira ◽  
Jurema Freire Lisboa de Castro ◽  
Elaine Judite de Amorim Carvalho ◽  
Oslei Paes de Almeida ◽  
...  
Keyword(s):  
Literature Review ◽  
Oral Cavity ◽  
Rare Case ◽  
English Language ◽  
Glomus Tumor ◽  
Benign Neoplasm ◽  
Upper Lip ◽  
Middle Aged Adults ◽  
Glomus Body ◽  
Language Literature

Abstract Glomus tumor is a benign neoplasm composed of a perivascular proliferation of glomic cells that resembles the normal glomus body. Usually, it appears as a solitary, symptomatic small blue-red nodule, located in the deep dermis or subcutis of upper or lower extremities of young to middle-aged adults. Cases affecting the oral cavity are very rare, with only 23 well-documented cases reported in the English-language literature. Herein, we present a rare case of glomus tumor of the upper lip, and review the literature of cases involving the mouth.

scholarly journals Giant Cell Fibroma of Tongue: Understanding the Nature of an Unusual Histopathological Entity

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Wanjari Ghate Sonalika ◽  
Anshuta Sahu ◽  
Suryakant C. Deogade ◽  
Pushkar Gupta ◽  
Dinesh Naitam ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Oral Cavity ◽  
Giant Cell ◽  
Rare Case ◽  
Giant Cells ◽  
Basic Process ◽  
Broad Category ◽  
Histopathological Features

Giant cell fibroma (GCF) is a rare case with unique histopathology. It belongs to the broad category of fibrous hyperplastic lesions of the oral cavity. It is often mistaken with fibroma and papilloma due to its clinical resemblance. Only its peculiar histopathological features help us to distinguish it from them. The origin of the giant cell is still controversial. Data available is very sparse to predict the exact behavior. Hence, we report a case of GCF of tongue in a 19-year-old male. Special emphasis is given to understand the basic process of development of the lesion, nature of giant cells, and also the need for formation of these peculiar cells. Briefly, the differential diagnosis for GCF is tabulated.

A Rare Case of Congenital Ewing Sarcoma/PNET of the Scapula

2014 ◽  
Vol 36 (2) ◽  
pp. e134-e135 ◽  
Author(s):  
Sree Rekha Jinkala ◽  
Debdatta Basu ◽  
Dinesan Mathath ◽  
Biswajit Dubashi ◽  
Arpita Bhaumik
Keyword(s):  
Ewing Sarcoma ◽  
Rare Case

Epidermoid Cyst of the Buccal Mucosa: A Case Report

2007 ◽  
Vol 8 (3) ◽  
pp. 90-96 ◽  
Author(s):  
Fatih Ozan ◽  
Hidayet Burak Polat ◽  
Sinan Ay ◽  
Fahrettin Goze
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Buccal Mucosa ◽  
Epidermoid Cyst ◽  
Rare Case ◽  
Neck Region ◽  
Facial Asymmetry ◽  
Left Cheek ◽  
Review Of The Literature ◽  
Head And Neck Region

Abstract Aim The purpose of this article is to describe a rare case of an epidermoid cyst in the buccal cheek region and a review of the literature. Background Dermoid and epidermoid cysts are developmental pathologies occurring in the head and neck region with an incidence ranging from 1.6% to 6.9%, and both cysts reported in less than 0.01% of all oral cavity cysts. Report A rare case of an epidermoid cyst originating from the buccal mucosa in a 38-year-old woman with a complaint of swelling and facial asymmetry in the left cheek just distal to the commissure for six months is presented in this report. Citation Ozan F, Polat HB, Ay S, Goze F. Epidermoid Cyst of the Buccal Mucosa: A Case Report. J Contemp Dent Pract 2007 March;(8)3:090-096.

Pleomorphic adenoma of the nasal septum

1999 ◽  
Vol 113 (5) ◽  
pp. 483-485 ◽  
Author(s):  
P. Jassar ◽  
N. D. Stafford ◽  
A. W. MacDonald
Keyword(s):  
Oral Cavity ◽  
Head And Neck ◽  
Salivary Glands ◽  
Pleomorphic Adenoma ◽  
Clinical Management ◽  
Nasal Septum ◽  
Rare Case ◽  
Minor Salivary Glands ◽  
Review Of The Literature ◽  
Upper Aerodigestive Tract

AbstractPleomorphic adenoma is the commonest benign tumour of the major salivary glands. It can also occur in minor salivary glands, mainly in the oral cavity, but also in other sites in the head and neck both within and outwith the upper aerodigestive tract. We present a rare case of pleomorphic adenoma of the nasal septum with consideration of the clinical management and a review of the literature.

Sign in / Sign up

Export Citation Format

Share Document