scholarly journals Giant Lipoma of Posterior Cervical Region

2014 ◽  
Vol 2014 ◽  
pp. 1-2
Author(s):  
Mahendra Singh ◽  
Ashish Saxena ◽  
Lovekesh Kumar ◽  
Snehal K. Karande ◽  
Yuvraj Kolhe
Keyword(s):  
Soft Tissue ◽  
Rare Case ◽  
Neck Region ◽  
Soft Tissue Tumors ◽  
Malignant Potential ◽  
Cervical Region ◽  
Head And Neck Region ◽  
Giant Lipoma ◽  
Benign Nature ◽  
Slow Growing

Lipomas are the slow growing soft tissue tumors of benign nature. They commonly grow on torso and extremities but may also develop in head and neck region. Rarely lipomas can grow to acquire gigantic proportions, turning into an entity termed as giant lipoma. Such lipomas are entitled to immediate attention as they have a relatively high malignant potential. We report a rare case of giant cervical lipoma in an elderly gentleman, followed by a brief discussion on diagnosis and management of the disorder.

scholarly journals Extremely rare case of retropharyngeal space benign plexiform schwannoma - Excised through Smith- Robinson Approach

2020 ◽  
Vol 11 ◽  
pp. 182
Author(s):  
Rajendra Sakhrekar ◽  
Vishal Peshattiwar ◽  
Ravikant Jadhav ◽  
Bijal Kulkarni ◽  
Sanjiv Badhwar ◽  
...  
Keyword(s):  
Cervical Spine ◽  
Rare Case ◽  
Neck Region ◽  
Retropharyngeal Space ◽  
Case Description ◽  
Head And Neck Region ◽  
Plexiform Schwannoma ◽  
Spine Mr ◽  
The Right ◽  
Slow Growing

Background: Approximately 25–45% of schwannomas are typically slow-growing, encapsulated, and noninvasive tumors that occur in the head-and-neck region where they rarely involve the retropharyngeal space. Here, we report deep-seated benign plexiform schwannoma located in the retropharyngeal C2-C5 region excised utilizing the Smith-Robinson approach. Case Description: A 30-year-old male presented with dysphagia and impaired phonation attributed to an MR documented C2-C5 retropharyngeal schwannomas. On examination, the lesion was soft, deep seated, and extended more toward the right side of the neck. Utilizing a right-sided Smith-Robinson’s approach, it was successfully removed. The histopathology confirmed the diagnosis of a plexiform schwannoma. Conclusion: Retropharyngeal benign plexiform schwannomas are rare causes of dysphagia/impaired phonation in the cervical spine. MR studies best document the size and extent of these tumors which may be readily resected utilizing a Smith-Robinson approach.

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 Rare extracranial localizations of the head and neck schwannomas

2010 ◽  
Vol 67 (7) ◽  
pp. 596-599
Author(s):  
Milan Jovanovic ◽  
Ljiljana Cvorovic ◽  
Rastislav Poljovka ◽  
Aleksandar Oroz ◽  
Ljubomir Pavicevic
Keyword(s):  
Head And Neck ◽  
Neck Region ◽  
Soft Tissue Tumors ◽  
Autonomic Nerves ◽  
Head And Neck Region ◽  
Delay In Diagnosis ◽  
Benign Soft Tissue Tumors ◽  
Indispensable Tool ◽  
Slow Growing ◽  
Nerve Of Origin

Introduction. Schwannomas are tumors of neurogenic origin, that arise from Schwann cells which surround peripheral, cranial and autonomic nerves. Schwannomas account for only 5% of all benign soft tissue tumors, and 25-45% of extracranial schwannomas are present in the head and neck region. They are usually classified according to the nerve of origin and the site within the head and neck. Case report. We presented extremely rare extracranial localizations of schwannomas and discussed about diagnosis and management of these tumors. Conclusion. Schwannomas are slow-growing tumors and late symptoms appearance may cause a delay in diagnosis and treatment of patients with these tumors. An appropriate diagnostic protocol is indispensable tool in performing a differential diagnosis of malignant from benign lesions. Choice of surgical approach depends on schwannomas localization.

Unusual presentation of lipoma on the tongue

2020 ◽  
Vol 13 (4) ◽  
pp. e232485
Author(s):  
Beena R Varma ◽  
Krishna Santhosh Kumar ◽  
Rhea Susan Verghese ◽  
Mahija Janardhanan
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Neck Region ◽  
Review Of Literature ◽  
Diagnostic Features ◽  
Soft Tissue Neoplasm ◽  
Head And Neck Region ◽  
Physiological Processes ◽  
Large Size ◽  
Slow Growing

Lipomas are benign soft tissue neoplasm which rarely occur in the oral cavity. Of the total reported cases of lipoma, only about 15% to 20% of cases have occurred in the head and neck region and the tongue is an even rarer site with only about 4% of the reported cases occurring in that region. They are slow growing and usually asymptomatic in nature. When it grows to a large size, it can hinder the physiological processes that are associated with the area. This case report describes the diagnostic features of tongue lipoma with a brief review of literature.

Intramuscular Hemangioma of the sternocleidomastoid muscle: A Rare Unusual Neck Mass

2020 ◽  
Vol 13 (1) ◽  
pp. 78-82
Author(s):  
Brihaspati Sigdel ◽  
Rajesh Maharjhan ◽  
Tulika Dubey ◽  
Bhima Neupane
Keyword(s):  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Neck Mass ◽  
Sternocleidomastoid Muscle ◽  
Benign Tumors ◽  
Head And Neck Region ◽  
Intramuscular Hemangioma ◽  
Slow Growing ◽  
Extensive Involvement

Hemangiomas of the head and neck region comprise about 60 to 70% of all benign tumors. Intramuscular hemangioma is a rare, slow-growing, angiomatous tumor. We report a rare case of an Intramuscular Hemangioma of Right sternocleidomastoid muscle in a six years old girl presenting for four years and with extensive involvement necessitating excision. Microscopic excision reduces the risk of recurrence.

scholarly journals Intraoral Superficial Angiomyxoma of the Upper Alveolus: Report of a Unique Case

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Ravindra S. V. ◽  
M. Srinivasa Raju ◽  
Sunitha J. D. ◽  
Neeraj Taneja ◽  
Sunira Chandra ◽  
...  
Keyword(s):  
Head And Neck ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Neck Region ◽  
Malignant Potential ◽  
Mesenchymal Tumors ◽  
Unique Case ◽  
Head And Neck Region ◽  
Floor Of The Mouth ◽  
Local Recurrences

Angiomyxomas are relatively a group of uncommon myxoid mesenchymal tumors characterized by frequent local recurrences and show lack of malignant potential. Basically three types of angiomyxomas are recognized superficial, aggressive, and angiomyofibroblastoma. Though the angiomyxomas are rarely reported in the head and neck region, the paper shows reported cases intraorally in the buccal mucosa and floor of the mouth. Here, the authors report a rare case of angiomyxoma presenting as a growth in the upper posterior alveolar mucosa.

scholarly journals Solid Variant of Alveolar Rhabdomyosarcoma of Nasal Cavity

2020 ◽  
Vol 18 (1) ◽  
pp. 102-104
Author(s):  
A Bhattarai ◽  
BL Shrestha ◽  
A Dhakal
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Ct Scan ◽  
Nasal Cavity ◽  
Head And Neck ◽  
Neck Region ◽  
Soft Tissue Tumors ◽  
Alveolar Rhabdomyosarcoma ◽  
Head And Neck Region ◽  
Nasal Mass

Rhabdomyosarcoma comprises about half of the soft tissue tumors. Approximately 40% of the alveolar subtype occur in the head and neck region. Patients present with unilateral nasal mass with/without lymphadenopathy and with/without orbital manifestations. Diagnosis is aided radiologically by CT scan, MRI along with biopsy and is confirmed by immunohistochemistry. Treatment involves surgical resection, chemotherapy, radiotherapy or a combination of these. In spite of treatments, however, the outcome is poor. This is a case report of 14-year-old male who presented with unilateral nasal mass with proptosis of right eye who was eventually diagnosed as a case of alveolar rhabdomyosarcoma of solid variant.

scholarly journals A rare case of a benign giant chondroid syringoma of nose

2020 ◽  
Vol 6 (8) ◽  
pp. 1549
Author(s):  
Neemu Hage ◽  
Jaimanti Bakshi ◽  
Mayank Rampal
Keyword(s):  
Neck Region ◽  
Needle Aspiration ◽  
Disease Entity ◽  
Head And Neck Region ◽  
Chondroid Syringoma ◽  
Large Size ◽  
Benign Nature ◽  
Slow Growing ◽  
Disease Free

<p class="abstract">Chondroid syringoma (CS) is a rare benign appendageal tumour of the skin, with histological similarities to pleomorphic adenoma of salivary glands. It typically presents as a slow growing nodular mass generally less than 3 cm, arising from the skin, predominantly in the head and neck region. We report a case of a 61-year-old male with a massive nasal mass attained over a period of 2 years. A fine needle aspiration of the lesion was suggestive of CS. It was excised completely under general anaesthesia. The postoperative histopathology was also consistent with CS. The patient was followed up on a regular basis and was rendered disease free till his last follow up at 4 months. Our purpose of reporting this case is to highlight the rarity of the disease entity, as well as the occasion of it acquiring a large size yet, maintaining its benign nature.</p>

Palatal Schwannoma: A Rare Case Report

2016 ◽  
Vol 8 (1) ◽  
pp. 29-31
Author(s):  
Nikhil Arora ◽  
PS Shahul Hameed
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Schwann Cells ◽  
Rare Case ◽  
Benign Tumor ◽  
Neck Region ◽  
Head And Neck Region ◽  
Nerve Sheath ◽  
Rare Case Report ◽  
Slow Growing

ABSTRACT Schwannoma is a benign tumor that originates from perineural Schwann cells of nerve sheath. They are solitary, wellencapsulated, slow-growing adjacent to the parental nerve but extrinsic to the nerve fascicles. Approximately 25 to 45% of all schwannomas are seen in the head and neck region and are found rarely in the oral cavity. Most of the intraoral schwannomas are located in the tongue. Palatal schwannoma is very rare as till date and only 16 cases have been reported; one such rare case we came across is reported here. How to cite this article Hameed PSS, Arora N, Malhotra V. Palatal Schwannoma: A Rare Case Report. Int J Otorhinolaryngol Clin 2016;8(1):29-31.

Dermatofibrosarcoma protuberans. A rare case involving the pediatric foot

1999 ◽  
Vol 89 (8) ◽  
pp. 419-423 ◽  
Author(s):  
JA Cione ◽  
B Lynn ◽  
J Boylan
Keyword(s):  
Rare Case ◽  
Malignant Neoplasm ◽  
Neck Region ◽  
Dermatofibrosarcoma Protuberans ◽  
Surgical Excision ◽  
Head And Neck Region ◽  
Pathologic Features ◽  
Pediatric Foot ◽  
Grade Malignancy ◽  
Slow Growing

Dermatofibrosarcoma protuberans is a rare, slow-growing, locally destructive, intermediate-grade malignancy that originates in the dermal layer of the skin. Dermatofibrosarcoma protuberans rarely metastasizes and has a marked tendency to recur following local surgical excision. The lesion is found most commonly on the trunk, on the proximal aspect of both the lower and upper extremities, and in the head and neck region. Dermatofibrosarcoma protuberans occurs most commonly in people between the ages of 20 and 50. This article describes the clinical and pathologic features of this rare, malignant neoplasm and describes a rare case of dermatofibrosarcoma protuberans involving the pediatric foot.

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