scholarly journals Large Neurilemmoma of Buccal Mucosa in a Child – A Rare Entity

2016 ◽  
Vol 24 (1) ◽  
pp. 39-42
Author(s):  
Sirshak Dutta ◽  
Neeraj Aggarwal ◽  
Avijit Choudhury ◽  
Ramanuj Sinha

  Introduction: Neurilemmoma or Schwannomas are benign tumour arising from the nerve sheath of myelinated nerve. Head neck neurilemmomas are not uncommon but intraoral region is very uncommon for this type of tumour. Case Report: A very rare case of buccal neurilemmoma in an eleven year old child, but much larger than other reported case is reported in the present article with review of literature. Discussion: Among the intraoral subsites, very few cases of neurilemmoma are reported to be situated in the buccal mucosa. Diagnostic dilemmas due to Fine needle aspiration cytology with features often resembling that of pleomorphic salivary adenomas are reported. The size of the tumour was larger than the cases reported in literature till date. The age of the patient was also much younger than the other reported cases, which made the present case unique.

2013 ◽  
Vol 5 (2) ◽  
pp. 8-9
Author(s):  
Hitesh Verma ◽  
RPS Punia

ABSTRACT Schwannoma is a benign, encapsulated tumor that is derived from schwann's cells. The most common site is parapharyngeal space of the neck; oropharyngeal occurrence is extremely rare. Fourteen year male boy presented with a history of difficulty in swallowing, more for solids for the last 8 months. The patient also had a change of voice for the last 5 months and was muffled in character. Examination showed single lobulated mass having smooth surface, of the size of approximately 5 × 4 cm and was arising from the tonsillolingual sulcus. The fine needle aspiration cytology from the lesion, reported to be schwannoma. The mass was excised completely under general anesthesia with the help of bipolar cautery. We report first case of schwannoma of tonsillolingual sulcus and also review the literature of the rare entity.


2019 ◽  
Vol 13 (1) ◽  
pp. 003
Author(s):  
Majed Basit Momin ◽  
Sandeep Satyanarayana ◽  
Anamika Aluri

Genitourinary tuberculosis is the second most common extrapulmonary tuberculosis (ETB), after lymph nodes. Isolated tuberculous epididymitis (ITE) is a rare entity among genitourinary tuberculosis and is defined as epididymitis without clinical evidence of either renal or prostate involvement. We present a case of epididymal tuberculosis in a 26 year old male which presented as a right scrotal mass. We discussed this case to emphasize that tuberculous etiology should also be considered in the differential diagnosis of scrotal mass besides malignancy, and an image guided fine needle aspiration cytology (FNAC) and stain for acid fast bacilli (AFB) play crucial role in diagnosis and treatment. IMC J Med Sci 2019; 13(1): 003


2021 ◽  
pp. 1-2
Author(s):  
Avinash Kumar ◽  
Manjari Kishore ◽  
Garima Sinha ◽  
S.K. Varma

Cysticercosis cellulosae is a systemic parasitic infection caused by the larval stage of pork tapeworm, taenia solium which involve humans as either a denitive or secondary host. It is a common disease in developing countries. The cases presenting as an isolated muscle mass is an extremely rare entity and demands documentation. Herein, we present a case of healthy pediatric patient who presented with unilateral cheek swelling which on ultrasound suggested a benign cystic lesion. The diagnosis was conrmed on ne needle aspiration cytology (FNAC).


2013 ◽  
Vol 5 (2) ◽  
pp. 98-99
Author(s):  
Hitesh Verma ◽  
RPS Punia

ABSTRACT Schwannoma is a benign, encapsulated tumor that is derived from schwann's cells. The most common site is parapharyngeal space of the neck; oropharyngeal occurrence is extremely rare. Fourteen year male boy presented with a history of difficulty in swallowing, more for solids for the last 8 months. The patient also had a change of voice for the last 5 months and was muffled in character. Examination showed single lobulated mass having smooth surface, of the size of approximately 5 × 4 cm and was arising from the tonsillolingual sulcus. The fine needle aspiration cytology from the lesion, reported to be schwannoma. The mass was excised completely under general anesthesia with the help of bipolar cautery. We report first case of schwannoma of tonsillolingual sulcus and also review the literature of the rare entity. How to cite this article Verma H, Dass A, Punia RPS. Schwannoma of Tonsillolingual Sulcus: First Case Report and Review of Literature. Int J Otorhinolaryngol Clin 2013;5(2): 98-99.


2013 ◽  
Vol 5 (01) ◽  
pp. 60-62 ◽  
Author(s):  
Chaithra R Jadhav ◽  
N R Angeline ◽  
Bipin Kumar ◽  
Ramachandra V Bhat ◽  
G Balachandran

ABSTRACTSchwannoma affect mainly head, neck, and flexor aspect of the limbs. Neurogenic tumors arising from the brachial plexus are rare and axillary schwannoma is extremely uncommon. Cystic degeneration is common in longstanding cases and which when aspirated may yield only macrophages or lymphocytes leading to false diagnosis of the case in spite of strong clinical suspicion. We report one such rare case of a solitary axillary schwannoma with extensive cystic degeneration, which was misdiagnosed on fine needle aspiration cytology and subsequently confirmed by the histopathological examination and immunohistochemistry.


2012 ◽  
Vol 4 (01) ◽  
pp. 056-058 ◽  
Author(s):  
Arvind Kinger ◽  
Mallika Kawatra ◽  
Tej Singh Chaudhary

ABSTRACTA 30-year-old female presented with a painless solitary swelling at right lateral border of tongue of 2-month duration. Fine-needle aspiration cytology was nonconclusive. Excision biopsy was done. Histopathology revealed cysticercosis cellulosae and parasite visualized in the slide with tongue muscles. Lingual cysticercosis is rare and therefore its literature is reviewed and discussed.


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