scholarly journals A Case of Lymphoepithelial Carcinoma Originating in the Submandibular Gland

2021 ◽  
Vol 37 (2) ◽  
pp. 81-85
Author(s):  
Sun Hong Kim ◽  
Geun Jeon Kim ◽  
Hyun Il Shin ◽  
Dong Il Sun
Keyword(s):  
Nasopharyngeal Carcinoma ◽  
Head And Neck ◽  
Submandibular Gland ◽  
Malignant Tumor ◽  
Neck Region ◽  
Lymphoepithelial Carcinoma ◽  
Head And Neck Region ◽  
Tumor Mass ◽  
Undifferentiated Nasopharyngeal Carcinoma

Lymphoepithelial carcinoma is an extremely rare malignant tumor, especially those localized at the head and neck region. The histological prototype of lymphoepithelial carcinoma is undifferentiated nasopharyngeal carcinoma. Herein, we report a case of a tumor localized in the left submandibular gland in a 20-year-old male. The tumor mass was surgically excised with the submandibular gland, and the specimen was pathologically confirmed to be lymphoepithelial carcinoma.

Oral Rehabilitation Following Removal of a Rhabdomyosarcoma and Subsequent Microstomia: A Case Report

2011 ◽  
Vol 37 (3) ◽  
pp. 353-360 ◽  
Author(s):  
Hakan Bilhan ◽  
Onur Geckili ◽  
Belir Atalay ◽  
Selda Arat
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Dental Implants ◽  
Malignant Tumor ◽  
Dental Treatment ◽  
Neck Region ◽  
Embryonal Rhabdomyosarcoma ◽  
Oral Rehabilitation ◽  
Head And Neck Region ◽  
Hybrid Prosthesis

Abstract Rhabdomyosarcoma is a malignant tumor that is most often seen in children younger than 15 years of age. This pathology is found mainly in the head and neck region. Treatment of rhabdomyosarcoma at early stages of life usually affects the dental and osseous development of children. Because of impaired development, microstomia can arise, making dental treatment more difficult. This article presents a patient with microstomia caused by resection of an embryonal rhabdomyosarcoma in the nasolabial region. The patient was treated with 5 dental implants and fixed hybrid prosthesis in the maxilla and 2 implants supporting an overdenture in the mandible.

scholarly journals The immunological parameters in the patient with malignant tumor of head and neck region.

1987 ◽  
Vol 33 (2) ◽  
pp. 290-296
Author(s):  
Hitoshi TANABE ◽  
Masamichi IDA ◽  
Teruyo FUKUDA ◽  
Kasuke NAKASHIMA ◽  
Fumihiko SHINOZAKI
Keyword(s):  
Head And Neck ◽  
Malignant Tumor ◽  
Neck Region ◽  
Immunological Parameters ◽  
Head And Neck Region

scholarly journals The effectiveness of oral propranolol for infantile hemangioma on the head and neck region: A case series

2021 ◽  
pp. 106120
Author(s):  
Prasetyanugraheni Kreshanti ◽  
Nandya Titania Putri ◽  
Valencia Jane Martin ◽  
Chaula Luthfia Sukasah
Keyword(s):  
Head And Neck ◽  
Case Series ◽  
Neck Region ◽  
Infantile Hemangioma ◽  
Head And Neck Region ◽  
Oral Propranolol

scholarly journals Therapeutic Strategies for Untreated Capillary Malformations of the Head and Neck Region: A Systematic Review and Meta-Analyses

2021 ◽  
Author(s):  
Gonca Cinkara ◽  
Ginger Beau Langbroek ◽  
Chantal M. A. M. van der Horst ◽  
Albert Wolkerstorfer ◽  
Sophie E. R. Horbach ◽  
...  
Keyword(s):  
Systematic Review ◽  
Head And Neck ◽  
Neck Region ◽  
Therapeutic Strategies ◽  
Head And Neck Region ◽  
Meta Analyses

scholarly journals Kimura disease: a rare cause of a recurrent cheek mass in a Jamaican man

2021 ◽  
Vol 2021 (4) ◽  
Author(s):  
Geoffrey Williams ◽  
Carlos Neblett ◽  
Jade Arscott ◽  
Sheena McLean ◽  
Shereika Warren ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Local Recurrence ◽  
Head And Neck ◽  
African Descent ◽  
Young Men ◽  
Neck Region ◽  
Serum Immunoglobulin ◽  
Western World ◽  
Kimura Disease ◽  
Head And Neck Region

Abstract Kimura disease (KD) is a chronic, inflammatory, benign disorder endemic to Asia that typically manifests as a triad of painless masses in the head and neck region, elevated eosinophils and serum immunoglobulin. It usually affects young men in their second and third decades of life and is rarely seen outside of the orient. This is a report of a case of KD in a young man of African descent who presented with a cheek mass. KD was not included in our differential diagnosis, and this report highlights the need to consider this entity, which can be easily missed due to its rarity in the Western world. There is no cure for the disease, and management includes medical and surgical modalities, but local recurrence or relapse is not uncommon.

scholarly journals Extranodal lymphoma of the head and neck: a pictorial essay

2019 ◽  
Vol 52 (4) ◽  
pp. 268-271
Author(s):  
Pinar Gulmez Cakmak ◽  
Gülsüm Akgün Çağlayan ◽  
Furkan Ufuk
Keyword(s):  
Lymph Nodes ◽  
Head And Neck ◽  
Neck Region ◽  
Extranodal Lymphoma ◽  
Imaging Findings ◽  
Head And Neck Region ◽  
Radiological Features ◽  
Extranodal Site ◽  
Pictorial Essay

Abstract Primary extranodal lymphoma is defined as a lymphoma at a solitary extranodal site, with or without involvement of the lymph nodes. The clinical and radiological features of extranodal lymphoma have been documented in recent studies. In this pictorial essay, we reviewed imaging findings of extranodal lymphoma in the head and neck region.

scholarly journals Concomitant cemento-osseous dysplasia and aneurysmal bone cyst of the mandible: a rare case report with literature review

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Han-Gyeol Yeom ◽  
Jung-Hoon Yoon
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Aneurysmal Bone Cyst ◽  
Cystic Lesion ◽  
Bone Cyst ◽  
Neck Region ◽  
Diagnostic Process ◽  
Simultaneous Occurrence ◽  
Head And Neck Region ◽  
Osseous Dysplasia

Abstract Background Concomitant cemento-osseous dysplasia (COD) and aneurysmal bone cyst (ABC) are rare in the head and neck region. In our search of the English language literature, we found only one case report describing the simultaneous occurrence of COD and ABC in the head and neck region. Here, we report a case of COD associated with ABC. Further, we performed a systematic search of the literature to identify studies on patients with COD associated with nonepithelial lined cysts of the jaws. Case presentation The patient was a 32-year-old woman who was referred from a private dental clinic because of a cystic lesion below the mandibular right first molar. She had no pain or significant systemic disease. After performing panoramic radiography and cone-beam computed tomography, the imaging diagnosis was COD with a cystic lesion, such as ABC or solitary bone cyst. Excisional biopsy was performed, which revealed concomitant COD and ABC. Conclusion This case of ABC associated with COD provides insight for the diagnostic process of radiographically mixed lesions with cystic changes.

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