scholarly journals Leiomyosarcoma of Maxillary Sinus – A Rare Clinical Entity

2018 ◽  
Vol 2 (1) ◽  
pp. 001-005
Author(s):  
Sah BP
Keyword(s):  
Maxillary Sinus ◽  
Clinical Entity ◽  
Rare Clinical Entity

scholarly journals Maxillary sinus arteriovenous malformation: A rare clinical entity

2013 ◽  
Vol 14 (1) ◽  
pp. 47-50 ◽  
Author(s):  
Jihène Marrakchi ◽  
Houda Chahed ◽  
Rym Zainine ◽  
Habiba Mizouni ◽  
Semia Sahtout ◽  
...  
Keyword(s):  
Arteriovenous Malformation ◽  
Maxillary Sinus ◽  
Clinical Entity ◽  
Rare Clinical Entity

scholarly journals Arteriovenous malformation of the maxillary sinus: a rare clinical entity

2020 ◽  
Vol 86 (6) ◽  
pp. 820-823 ◽  
Author(s):  
Dongwon Kim ◽  
Kyung-Un Choi ◽  
Hak-Jin Kim ◽  
Kyu-Sup Cho
Keyword(s):  
Arteriovenous Malformation ◽  
Maxillary Sinus ◽  
Clinical Entity ◽  
Rare Clinical Entity

Simultaneous antrochoanal and sphenochoanal polyps: a rare clinical entity

2005 ◽  
Vol 119 (2) ◽  
pp. 152-154 ◽  
Author(s):  
Muge Ozcan ◽  
Samet Ozlugedik ◽  
Aykut Ikinciogullari
Keyword(s):  
Maxillary Sinus ◽  
Surgical Management ◽  
Clinical Presentation ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Choanal Polyp ◽  
Sphenochoanal Polyp ◽  
First Time

Choanal polyps almost always appear as solitary growths and most commonly arise from the maxillary sinus. Sphenochoanal and ethmoidochoanal polyps are extremely rare. Co-existence of more than one choanal polyp is even more infrequent. We present a patient with an antrochoanal and an accompanying sphenochoanal polyp for the first time in the literature. We discuss the clinical presentation, pathogenesis and surgical management of this rare clinical entity.

scholarly journals Bronchoesophageal fistula secondary to esophageal diverticulum in an adult: a case report and literature review

2021 ◽  
Vol 49 (2) ◽  
pp. 030006052199223
Author(s):  
Xiaolin Zhang ◽  
Hongmei Jiao ◽  
Xinmin Liu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Respiratory Infections ◽  
Relevant Literature ◽  
Rare Condition ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Esophageal Diverticulum ◽  
Bronchoesophageal Fistula ◽  
Fatal Complications

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.

scholarly journals Primary tubercular caecal perforation: a rare clinical entity

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

scholarly journals Cartilaginous Choristoma of the Gingiva: A Rare Clinical Entity

2014 ◽  
Vol 2014 ◽  
pp. 1-4
Author(s):  
Ramalingam Suganya ◽  
Narasimhan Malathi ◽  
Subramani Vijaya Nirmala ◽  
Chinnaswami Ravindran ◽  
Harikrishnan Thamizhchelvan
Keyword(s):  
Connective Tissue ◽  
Histopathological Examination ◽  
Clinical Entity ◽  
Fibrous Connective Tissue ◽  
Rare Clinical Entity ◽  
Normal Cells ◽  
Connective Tissue Stroma

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.

scholarly journals Role of Immunotherapy in Pulmonary Angiosarcoma: A Case Report

2021 ◽  
pp. 797-801
Author(s):  
Quang Tien Nguyen ◽  
Anh Tuan Pham ◽  
Thuy Thi Nguyen ◽  
Tam Thi Thanh Nguyen ◽  
Ky Van Le
Keyword(s):  
Case Report ◽  
Poor Prognosis ◽  
Checkpoint Inhibitor ◽  
Therapeutic Strategies ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Excellent Response ◽  
First Case

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.

Acquired postganglionic cholinergic dysautonomia – A rare clinical entity

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