scholarly journals Spontaneous chylothorax due to a left neck mass: Case report and literature review of a rare clinical entity

Author(s):  
William Spiller
2021 ◽  
Vol 18 ◽  
pp. 100261
Author(s):  
A.G. Thangirala ◽  
D. Chelius ◽  
G. Holzmann-Pazgal ◽  
E.M. Lambert

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.


2019 ◽  
Vol 125 ◽  
pp. 113-115
Author(s):  
Jaibir S. Pannu ◽  
Zachary Farhood ◽  
Jennifer Brinkmeier ◽  
Dary J. Costa

2001 ◽  
Vol 91 (7) ◽  
pp. 373-378 ◽  
Author(s):  
William P. Goforth ◽  
Troy D. Overbeek

A cylindrical autogenous diaphyseal bone graft from the neighboring second and fifth metatarsals to correct brachymetatarsia of the third and fourth metatarsals was last described by Biggs in 1979. The authors present a literature review and case report for the treatment of the rare clinical entity of brachymetatarsia. (J Am Podiatr Med Assoc 91(7): 373-378, 2001)


2017 ◽  
Vol 97 ◽  
pp. 760.e9-760.e12 ◽  
Author(s):  
Aneesh Mohimen ◽  
Santhosh Kumar Kannath ◽  
E.R. Jayadevan

ORL ro ◽  
2017 ◽  
Vol 2 (35) ◽  
pp. 24
Author(s):  
Daniel Mirea ◽  
Loredana Mitran ◽  
Daniela Safta ◽  
Cornelia Niţipir ◽  
Bogdan Mocanu ◽  
...  

2020 ◽  
Vol 33 ◽  
pp. 101354
Author(s):  
Angela Piccirilli ◽  
Federico Romantini ◽  
Pietro Saldutto ◽  
Guevar Maselli ◽  
Giuseppe Paradiso ◽  
...  

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.


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