Schwannoma of Tonsillolingual Sulcus: First Case Report and Review of Literature

2013 ◽  
Vol 5 (2) ◽  
pp. 8-9
Author(s):  
Hitesh Verma ◽  
RPS Punia
Keyword(s):  
Smooth Surface ◽  
Parapharyngeal Space ◽  
Needle Aspiration ◽  
Rare Entity ◽  
Review Of Literature ◽  
Common Site ◽  
Aspiration Cytology ◽  
First Case ◽  
History Of ◽  
Needle Aspiration Cytology

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.

Schwannoma of Tonsillolingual Sulcus: First Case Report and Review of Literature

2013 ◽  
Vol 5 (2) ◽  
pp. 98-99
Author(s):  
Hitesh Verma ◽  
RPS Punia
Keyword(s):  
Case Report ◽  
Parapharyngeal Space ◽  
Needle Aspiration ◽  
Rare Entity ◽  
Review Of Literature ◽  
Common Site ◽  
Aspiration Cytology ◽  
First Case ◽  
History Of ◽  
Needle Aspiration Cytology

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.

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
Keyword(s):  
Buccal Mucosa ◽  
Rare Case ◽  
Needle Aspiration ◽  
Rare Entity ◽  
Review Of Literature ◽  
Aspiration Cytology ◽  
Myelinated Nerve ◽  
Nerve Sheath ◽  
Needle Aspiration Cytology ◽  
Head Neck

  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.

scholarly journals Case of Lingual Cysticercosis and Review of Literature

2012 ◽  
Vol 4 (01) ◽  
pp. 056-058 ◽  
Author(s):  
Arvind Kinger ◽  
Mallika Kawatra ◽  
Tej Singh Chaudhary
Keyword(s):  
Fine Needle Aspiration ◽  
Fine Needle Aspiration Cytology ◽  
Needle Aspiration ◽  
Excision Biopsy ◽  
Review Of Literature ◽  
Aspiration Cytology ◽  
Lateral Border ◽  
Fine Needle ◽  
Tongue Muscles ◽  
Needle Aspiration Cytology

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.

scholarly journals Primary retroperitoneal mullerian adenocarcinoma

Rare Tumors ◽  
2010 ◽  
Vol 2 (1) ◽  
pp. 16-19 ◽  
Author(s):  
Ayman Elnemr ◽  
Yutaka Yonemura ◽  
Masaya Shinbo ◽  
Eisei Nishino
Keyword(s):  
Abdominal Mass ◽  
Needle Aspiration ◽  
Cystic Mass ◽  
High Serum ◽  
Aspiration Cytology ◽  
Positron Emission ◽  
Pet Scanning ◽  
History Of ◽  
Needle Aspiration Cytology ◽  
Primary Retroperitoneal

Mullerian tumors are extremely rare malignancies in the retroperitoneum. We report a case of a 46-year old woman who presented with an eight year history of lower abdominal mass. Ultrasonography (US) and computed tomography (CT) demonstrated a 15×10 cm cystic mass in the left lower retroperitoneum. As serial percutaneous needle aspiration cytology was negative for malignancy, she was observed for seven years. Eleven months ago, the mass was excised. The histopathology was reported as mucinous adenocarcinoma of the retroperitoneum. Six cycles of intraperitoneal (IP) chemotherapy was administered during the last six months after diagnosis of recurrence by aspiration cytology and high serum tumor markers (CEA, CA19-9). A few days ago, positron emission tomographic (PET) scanning showed evidence of local recurrence and single vertebral metastasis, so she was admitted again for systemic chemotherapy. Meticulous revision of additional sections of the tumor revealed papillary, serous, mucinous, and endometrioid subtypes of the mullerian adenocarcinoma. To our knowledge, there has been no similar case described in the literature.

scholarly journals Hyalinizing Granuloma: An Unusual Case of a Pulmonary Mass

2010 ◽  
Vol 2010 ◽  
pp. 1-3 ◽  
Author(s):  
Viviane Brandão ◽  
Edson Marchiori ◽  
Gláucia Zanetti ◽  
Guilherme Abdalla ◽  
Nina Ventura ◽  
...  
Keyword(s):  
Unusual Case ◽  
Histopathological Examination ◽  
Laboratory Data ◽  
Previous Treatment ◽  
Needle Aspiration ◽  
Open Lung Biopsy ◽  
Aspiration Cytology ◽  
Ct Guided ◽  
History Of ◽  
Needle Aspiration Cytology

We describe the case of pulmonary hyalinizing granuloma in a 34-year-old asymptomatic man who presented with a pulmonary nodule apparent by chest radiography and computed tomography (CT). He had a history of previous treatment for tuberculosis. His laboratory data were normal. Bronchoscopy and CT-guided percutaneous transthoracic fine needle aspiration cytology were inconclusive. The diagnosis was revealed after the histopathological examination of an open lung biopsy.

scholarly journals Nodal histiocytic disorder in children: report of three cases and review of literature

2020 ◽  
Vol 36 (1) ◽  
Author(s):  
Indumathi Ainer ◽  
Hardip Singh Gendeh ◽  
Salina Binti Husain ◽  
Khadijah Mohd Nor
Keyword(s):  
Cervical Lymph Node ◽  
Final Diagnosis ◽  
Needle Aspiration ◽  
Neck Mass ◽  
Review Of Literature ◽  
Aspiration Cytology ◽  
Case Presentation ◽  
Massive Lymphadenopathy ◽  
Lymph Node Enlargement ◽  
Needle Aspiration Cytology

Abstract Background Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis. Case presentation Here, we report three pediatric cases: one of Langerhans cell histiocytosis and two of sinus histiocytosis and massive lymphadenopathy with neck mass as initial presentation. The final diagnosis was made with fine needle aspiration cytology, biopsy, and ancillary tests. Conclusion Biopsy and immunohistochemistry studies are recommended for determining subtypes of histiocytosis and further management of patient.

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