scholarly journals Rare cervical nerve root C2-C3 schwannoma

2017 ◽  
Vol 3 (4) ◽  
pp. 1123
Author(s):  
Chandra Veer Singh ◽  
Shravan Shetty ◽  
R. K. Deshpande ◽  
Priyank Patel
Keyword(s):  
Head And Neck ◽  
Nerve Root ◽  
Neck Region ◽  
Cervical Nerve ◽  
Shoulder Stiffness ◽  
Head And Neck Region ◽  
Posterior Neck ◽  
C2 Nerve Root ◽  
Lateral Neck Swelling ◽  
Rule Out

<p class="abstract"><span lang="EN-IN">10% of schwannomas that occur in the head and neck region mostly originate from the vagus or sympathetic nervous system whereas those arising from C2 nerve root are extremely rare. Extracranial schwannomas in the head and neck region are rare neoplasms. Diagnosis is established by imaging studies such as magnetic resonance imaging or computed tomography, while FNAC is used to rule out other condition. Histopathology gives definitive diagnosis. The accepted treatment for these tumors is surgical resection with preservation of the neural pathway. We present a rare case of cervical nerve (C2-C3) root schwannoma of 50 year old male who presented with right lateral neck swelling with pain  radiating to right shoulder associated with right shoulder stiffness</span>. The swelling which also had an intervertebral part <span lang="EN-IN">was removed successfully through a posterior neck incision with no post-operative neurological symptoms.</span></p>

scholarly journals A rare clinical case: schwannoma of tongue

2019 ◽  
Vol 5 (3) ◽  
pp. 789
Author(s):  
Chandra Veer Singh ◽  
Sheetal Radia ◽  
Saalim Sheikh ◽  
Vijay Haribhakti
Keyword(s):  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Surgical Excision ◽  
Imaging Studies ◽  
Head And Neck Tumours ◽  
Head And Neck Region ◽  
Complete Surgical Excision ◽  
Slow Growing ◽  
Rule Out

<p class="abstract">Schwannoma are slow growing tumours, which can arise from any peripheral nerve. 10% of schwannomas that occur in the head and neck region mostly originate from the vagus or sympathetic nervous system. Extracranial schwannomas in the head and neck region are rare neoplasm. Intraoral schwannoma are only 1% of the all head and neck tumours. Diagnosis is established by imaging studies such as magnetic resonance imaging or computed tomography, while FNAC is used to rule out other conditions. We report a rare case of lingual schwannomas generally present as a painless lump schwannoma of the tongue in a 27-year-old male complaining of asymptomatic swelling over a posterolateral surface of the tongue, treated by complete surgical excision. The diagnosis was established on the basis of clinical, histopathological, and immunohistochemical examination. We report a rare case of schwannoma over the posterolateral surface of tongue. Prognosis is good for the patient when this condition is correctly diagnosed as the condition rarely recurs after complete resection.</p>

scholarly journals Bronchogenic cyst of the posterior neck mimicking lymphatic malformation

2021 ◽  
Author(s):  
Addison Yee ◽  
Sriram Navuluri ◽  
Ravi Sun ◽  
Miki Lindsey ◽  
Laura Gonzalez-krellwitz ◽  
...  
Keyword(s):  
Head And Neck ◽  
Bronchogenic Cyst ◽  
Neck Region ◽  
Cystic Mass ◽  
Lymphatic Malformation ◽  
Head And Neck Region ◽  
Posterior Neck ◽  
Bronchogenic Cysts

Bronchogenic Cysts are embryologic malformations of the foregut and are rarely found head and neck region. Here we present a case of an upper scapular/lower posterior neck cystic mass which was initially suspicious for lymphatic malformation but confirmed by pathology to be a ectopic bronchogenic cyst.

scholarly journals Venous Malformation in the Neck

2017 ◽  
Vol 25 (3) ◽  
pp. 173-175
Author(s):  
Bijan Kumar Adhikary ◽  
Sohag Kundu ◽  
Bhaskar Ghosh ◽  
Ramanuj Sinha
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Venous Malformation ◽  
Treatment Options ◽  
Neck Region ◽  
Vascular Lesion ◽  
Lateral Neck ◽  
Neck Swelling ◽  
Head And Neck Region ◽  
Lateral Neck Swelling

Introduction Venous malformation is a benign vascular lesion. Approximately 40% of such cases occur in head and neck. Case Report Venous malformation in a 19 year old man is reported, which presented as a lateral neck swelling. Discussion The venous malformation in the head and neck region may confuse the surgeon in distinguishing it from its other common congeners e.g. hemangioma, lymphangioma etc. and may also cause dilemma regarding its treatment modality. Treatment options include surgery, laser therapy, sclerotherapy or a combination depending upon the complexity of the lesion.

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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