Congenital Midline Cervical Cleft — A Rare Clinical Entity

1994 ◽  
Vol 111 (1) ◽  
pp. 148-149 ◽  
Author(s):  
Nelson C. Goldman ◽  
Kelvin K. W. Liu ◽  
Kim H. Lee
2021 ◽  
Vol 1 (1) ◽  
pp. 34-36
Author(s):  
Ahmed H. Al-Salem ◽  
Abdullah O. Bawazir ◽  
Nawaf F. Halabi ◽  
Razan Bawazir

Congenital midline cervical cleft is an extremely rare anterior neck defect. We describe a case of a male newborn with midline cervical cleft outlining aspects of diagnosis and stressing the importance of early diagnosis and surgical treatment.


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 ◽  
...  

2010 ◽  
Vol 2 (3) ◽  
pp. 125 ◽  
Author(s):  
AtulK Khandelwal ◽  
DevendraS Pawar ◽  
Rajeev Sen ◽  
Sachit Sharma ◽  
SantoshK Singh

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