scholarly journals Laryngeal Synovial Sarcoma: a Rare Clinical Entity

2020 ◽  
Vol 11 (S1) ◽  
pp. 125-127
Author(s):  
Sravan Kumar ◽  
Srijan Shukla ◽  
S. Avinash ◽  
Daphne Fonseca ◽  
Hemant Nemade ◽  
...  
2015 ◽  
Vol 6 (2) ◽  
pp. 49-52
Author(s):  
Sudhir Naik ◽  
Rajshekar Halkud ◽  
KT Siddappa ◽  
A Nanjundappa ◽  
Siddharth Biswas ◽  
...  

ABSTRACT Background Head and neck synovial sarcoma (SS) amounts to 6.8% of all total body SS, with high incidences in the hypopharynx, postpharyngeal region and the parapharyngeal space. Also, incidences of SS in the tongue, soft palate, mandible, buccal mucosa, floor of the mouth, lungs, thymus, trunk and posterior peritoneum are reported. Case report We report a case of 12-year-old girl with swelling in the floor of the mouth for 2 months. The patient had difficulty in speech, tongue movements, poor oral hygiene due to food residue collecting around the tumor in the floor of the mouth. A smooth 4 × 4 cm globular mass arising from the floor of the mouth with the fine needle aspiration cytology (FNAC) as spindle cell neoplasm. Wide excision and immunohistology confirmed it as calcified synovial sarcoma, hence postoperative chemotherapy was given. There is no recurrence for the past 3 years. Conclusion Synovial sarcoma is a rare tumor in the oral cavity, which is slow growing and of variable aggressiveness. Immunohistological analysis confirming the diagnosis and wide surgical excision with adjuvant chemotherapy is the modality preferred in these cases. Recurrence is common in the first 2 years of therapy but can occur later also. How to cite this article Nanjundappa A, Naik SM, Halkud R, Chavan P, Siddappa KT, Biswas S. Synovial Sarcoma of the Floor of the Mouth: A Rare Clinical Entity with Review of Literature. Int J Head Neck Surg 2015;6(2):49-52.


2015 ◽  
Vol 30 (11) ◽  
pp. 801-804 ◽  
Author(s):  
Joshua Goldblatt ◽  
Pankaj Saxena ◽  
David C. McGiffin ◽  
Adam Zimmet

2021 ◽  
Vol 49 (2) ◽  
pp. 030006052199223
Author(s):  
Xiaolin Zhang ◽  
Hongmei Jiao ◽  
Xinmin Liu

Esophageal diverticulum with secondary bronchoesophageal fistula is a rare clinical entity that manifests as respiratory infections, coughing during eating or drinking, hemoptysis, and sometimes fatal complications. In the present study, we describe a case of bronchoesophageal fistula emanating from esophageal diverticulum in a 45-year-old man who presented with bronchiectasis. We summarize the characteristics of this rare condition based on a review of the relevant literature.


BMC Surgery ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Devendra K Jain ◽  
Gaurav Aggarwal ◽  
Parvinder S Lubana ◽  
Sonia Moses ◽  
Nitin Joshi

2014 ◽  
Vol 2014 ◽  
pp. 1-4
Author(s):  
Ramalingam Suganya ◽  
Narasimhan Malathi ◽  
Subramani Vijaya Nirmala ◽  
Chinnaswami Ravindran ◽  
Harikrishnan Thamizhchelvan

Choristomas are rare entities which are aggregates of microscopically normal cells or tissues in aberrant locations. They are a “heterotopic” rest of cells, as they appear as a tumor-like mass. Herein we report a case of cartilaginous choristoma in a 54-year-old male who presented with a swelling on right lower gingiva. The histopathological examination revealed features of a well circumscribed mass of mature cartilage in a dense fibrous connective tissue stroma.


2021 ◽  
pp. 797-801
Author(s):  
Quang Tien Nguyen ◽  
Anh Tuan Pham ◽  
Thuy Thi Nguyen ◽  
Tam Thi Thanh Nguyen ◽  
Ky Van Le

Pulmonary angiosarcoma is a rare clinical entity with a poor prognosis and no established therapeutic strategies. We present the first case to our knowledge of metastatic pulmonary angiosarcoma, treated with checkpoint inhibitor immunotherapy, and have an excellent response. Until now, patient has been treated with immunotherapy for 1 year, and his disease is stable and well-tolerated.


2021 ◽  
Vol 1 (2) ◽  
pp. 352
Author(s):  
MeenaChembil Kakkitampara ◽  
Madhukar Mohan ◽  
AnjuSivadasa Raju

2017 ◽  
Vol 13 (1) ◽  
Author(s):  
Yaping Wu ◽  
Yue Song ◽  
Rong Huang ◽  
Jiaan Hu ◽  
Xiaotong He ◽  
...  

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