scholarly journals Osteoma of mastoid part of right temporal bone with right nasochoanal polyposis: a rare case report

2018 ◽  
Vol 5 (1) ◽  
pp. 202
Author(s):  
K. V. Lokanath ◽  
Debaditya Basu ◽  
Abhinav Kuthiala
Keyword(s):  
Temporal Bone ◽  
Paranasal Sinuses ◽  
Rare Case ◽  
Surgical Excision ◽  
Benign Tumors ◽  
Rare Entity ◽  
Good Cosmetic Outcome ◽  
Complete Surgical Excision ◽  
Rare Case Report ◽  
Good Cosmetic

<p class="abstract">Osteomas are benign mesenchymal osteoblastic tumors of lamellar bones. In our practice, they are usually seen in the paranasal sinuses, mainly involving the frontal and ethmoidal sinus. Osteoma of the temporal bone is uncommon and when they occur, they are most commonly seen in the external auditory canal. Mastoid osteomas are a rare entity with incidence of 0.1 - 1% of all benign tumors of skull. They are slowing growing and usually asymptomatic. We report a rare case in a 28 years female patient who presented to us with right postauricular bony swelling of size 2.5×3 cms along with bilateral nasal obstruction. Patient was analyzed for her clinical condition, imaging details, treatment and surgical plan. Diagnosis of right mastoid osteoma with right nasochoanal polyposis was made after non-contrast computed tomography of temporal bone and paranasal sinuses respectively. Complete surgical excision of the osteoma along with endoscopic removal of the polypoidal tissue was done with good cosmetic outcome without recurrence.</p>

scholarly journals Extraocular Myocysticercosis Involving Levator Palpebrae Superioris-Superior Rectus Complex: A Rare case Report

2013 ◽  
Vol 4 (4) ◽  
pp. 36-39
Author(s):  
Sajid Ansari ◽  
Mukesh Kumar Gupta ◽  
Kaleem Ahmad ◽  
Kanchan Dhungel ◽  
Abhishek Kumar ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Rare Case ◽  
Medical Science ◽  
Surgical Excision ◽  
Extraocular Muscles ◽  
Science Volume ◽  
Ocular Involvement ◽  
Rare Entity ◽  
Rare Case Report ◽  
Levator Palpebrae

The ocular involvement of the cysticercosis is a rare entity involving eyelids, extraocular muscles, orbit, conjunctiva, anterior chamber, uvea, retina, vitreous and optic nerve. All the extraocular muscles are involved in myocysticercosis. Ultrasonography and Computed tomography are the imaging modalities for evaluation of ocular cysticercosis. The patients can be treated with systemic steroids and albendazole; however surgical excision is the treatment of choice. We report a rare case of extraocular myocysticercosis in nine years old boy diagnosed on ultrasonography and computed tomography. Asian Journal of Medical Science, Volume-4 (2013), Pages 36-39 DOI: http://dx.doi.org/10.3126/ajms.v4i4.8163 

scholarly journals Nasolabial hamartoma: a rare case report

2020 ◽  
Vol 6 (7) ◽  
pp. 1397
Author(s):  
D. Senthamarai Kannan ◽  
G. Soundara Rajan ◽  
Veerasigamani Narendrakumar ◽  
V. K. Sathiya
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Surgical Excision ◽  
The Body ◽  
Nasolabial Fold ◽  
Tissue Development ◽  
Inborn Errors ◽  
Complete Surgical Excision ◽  
Rare Case Report

<p class="abstract">Nasolabial cysts are rare, nonodontogenic soft tissue developmental cysts occur in the maxillary lip and nasal alar regions. Patients usually presents with an asymptomatic soft swelling with obliteration of the nasolabial fold. Due to it's origin from entrapped epithelium in an embryonic fusion plane developmentally, this cyst is considered to be a Hamartoma. Hamartomas are non-neoplastic malformations, or inborn errors of tissue development. They are characterized by an abnormal mixture of tissues indigenous to that area of the body. Complete surgical excision is the accepted method of treatment. This report aimed to present a case of nasolabial cyst hamartoma, which is rare in presentation.</p>

scholarly journals Multiple Calcified Scrotal Sebaceous Cysts: A Rare Case Presentation

2018 ◽  
Vol 7 (1) ◽  
pp. 1646
Author(s):  
Randeep Singh Lamba ◽  
Manjit Singh Uppal ◽  
Seema Mittal ◽  
Manu Kohli ◽  
Jagpreet Singh
Keyword(s):  
Rare Case ◽  
Surgical Excision ◽  
Case Presentation ◽  
Retention Cyst ◽  
Cosmetic Results ◽  
Excellent Outcome ◽  
Minimal Morbidity ◽  
Sebaceous Cyst ◽  
Complete Surgical Excision ◽  
Good Cosmetic

A sebaceous cyst is a retention cyst. The classical management of scrotal sebaceous cysts is complete surgical excision and in the current era and as expected from the patient from the doctor and as the duty of the doctor, excellent outcome, minimal morbidity with good cosmetic results.

scholarly journals Epiglottic dermoid cyst: a rare case report

2021 ◽  
Vol 7 (8) ◽  
pp. 1381
Author(s):  
Ramchandra . ◽  
C. B. Nandyal ◽  
Kiran Deshmukh
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Rare Case ◽  
English Literature ◽  
Age Groups ◽  
Neck Region ◽  
Surgical Excision ◽  
Complete Surgical Excision ◽  
Body Sensation ◽  
Rare Case Report

<p>Epiglottis dermoid cysts are generally benign lesions, which can affect all the age groups. Dermoid cysts arising from the head and neck region are rare, slow growing, and well-circumscribed neoplasm. Symptoms are non-specific and usually related to the size and the location of the lesion. A dermoid cyst of the epiglottis is extremely rare. To the best of our knowledge, only one case has been previously reported in the English literature and a total of three cases were presented in Russian literature in two studies. In our report, a middle-aged male presented with foreign body sensation in throat for 1-year and difficulty in swallowing for three months, mainly for solids. Thorough history, clinical examination and relevant investigation were done. Direct laryngoscopy was done and complete surgical excision was done. The aim of the case report is to present a rare case of epiglottic dermoid cyst, its clinical presentation, radio-logical features and surgical management.</p>

Monomorphic Adenoma of Posterior Palate: A Rare Case Report

2021 ◽  
Author(s):  
Abhinav Sharma
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Malignant Tumors ◽  
Minor Salivary Gland ◽  
Benign Tumors ◽  
Rare Entity ◽  
Present Case Report ◽  
Rare Case Report ◽  
Monomorphic Adenoma

Background: Minor salivary gland benign tumors account for a very small percentage of salivary gland tumors of which monomorphic adenomas are a rare entity. Methods and Findings: The present case report discusses a rare case report of an 18-year-old female patient diagnosed with monomorphic adenoma of the posterior palatal region. The diagnosis was reached after thorough radiographical and pathological investigations. Conclusion: Monomorphic Adenoma in a younger individual is a rare disorder and can be used as a collective term for benign or malignant tumors comprising of one type or even two types of cells.

scholarly journals Anesthetic Management of a Large Retroperitoneal Paraganglioma: A Rare Case Report

2020 ◽  
pp. 1-6
Author(s):  
R Arun Kumar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Anesthetic Management ◽  
Surgical Excision ◽  
Cardiovascular Complications ◽  
Palpable Mass ◽  
Complete Surgical Excision ◽  
Rare Case Report ◽  
Male Preponderance ◽  
Sporadic Tumors

Paragangliomas are rare tumors derived from the neural crest cells. Most of the paragangliomas occur as sporadic tumors. The commonest incidence occurs in the second and third decade of life with a slight male preponderance. Clinically patients with a retroperitoneal paraganglioma often present with back pain or a palpable mass. There is a 5% incidence of turning into malignancy and these tumors are associated with a high risk of morbidity and mortality from cardiovascular complications. Management for paragangliomas typically involves complete surgical excision. A multi-disciplinary approach is suggested for a better outcome of the procedure

scholarly journals Schwannoma of the cervical vagus nerve: a rare case report

2017 ◽  
Vol 4 (1) ◽  
pp. 263 ◽  
Author(s):  
Chandra Mohan Setty L. N.
Keyword(s):  
Peripheral Nerves ◽  
Rare Case ◽  
Relevant Literature ◽  
Surgical Excision ◽  
Neck Masses ◽  
Complete Surgical Excision ◽  
Complete Surgical Resection ◽  
Rare Case Report ◽  
Painless Mass ◽  
Nerve Of Origin

<p class="abstract"><span lang="EN-IN">Schwannomas, also called as neurilemomas, are well-encapsulated, slowly growing tumors that arise from schwann cells of peripheral nerves. Clinically, schwannomas present as asymptomatic, slowly enlarging lateral neck masses and so they tend to present late. The nerve of origin is not often made until the time of surgery. Preoperative diagnosis is aided by imaging studies such as magnetic resonance imaging and computed tomography. The treatment of choice of schwannomas of the neck typically involves complete surgical resection. Rapidly growing tumors with evidence of invasion, or complete loss of nerve function should trigger complete surgical excision of the tumor. Here, we report a rare case of cervical vagal schwannoma in a 45 year old female who got admitted with the complaint of a firm, painless mass on the left side of the neck. The management of the case is discussed along with the relevant literature.</span></p>

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

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>

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