scholarly journals COVID‐19 in a child with tuberculous airway compression

2020 ◽  
Vol 55 (9) ◽  
pp. 2201-2203
Author(s):  
Pierre Goussard ◽  
Regan S. Solomons ◽  
Savvas Andronikou ◽  
Lunga Mfingwana ◽  
Lilly M. Verhagen ◽  
...  
Keyword(s):  

2013 ◽  
Vol 96 (6) ◽  
pp. 2192-2197 ◽  
Author(s):  
Hyo Soon An ◽  
Eun Young Choi ◽  
Bo Sang Kwon ◽  
Gi Beom Kim ◽  
Eun Jung Bae ◽  
...  


2014 ◽  
Vol 35 (2) ◽  
pp. 137-140 ◽  
Author(s):  
Debnath Chatterjee ◽  
Joy L. Hawkins ◽  
Stig Somme ◽  
Henry L. Galan ◽  
Jeremy D. Prager ◽  
...  


2010 ◽  
Vol 39 (2) ◽  
pp. 206-207
Author(s):  
Fateh A. Elkhatib ◽  
Amer A. Alkhatib


2007 ◽  
Vol 205 (6) ◽  
pp. 813 ◽  
Author(s):  
Muhammad I. Aslam ◽  
Christopher D. Sutton ◽  
David C. Hunter
Keyword(s):  


2009 ◽  
Vol 39 (7) ◽  
pp. 694-702 ◽  
Author(s):  
Jaco du Plessis ◽  
Pierre Goussard ◽  
Savvas Andronikou ◽  
Robert Gie ◽  
Reena George


2020 ◽  
Vol 13 (4) ◽  
pp. e234374
Author(s):  
Muhammad Hassan Danish ◽  
Muhammad Wasif ◽  
Nasir Ud Din ◽  
Muhammad Sohail Awan

Malignant peripheral nerve sheath tumours of thyroid are rare entities that can present a diagnostic dilemma. We present the case of a patient who presented with neck mass with a history of multiple neck surgeries and airway compression. The patient’s previous histopathology was mistaken for Riedel’s thyroiditis in an outside hospital, which delayed appropriate treatment leading to suffering on part of the patient and frustration on part of the physician. We emphasise that rare malignancies should be considered in rapidly growing neck masses that are causing airway compression, and histopathology of such tumours should be reported by expert pathologists.



2019 ◽  
Vol 10 (5) ◽  
pp. 558-564
Author(s):  
Christina L. Greene ◽  
Richard D. Mainwaring ◽  
Douglas Sidell ◽  
Michal Palmon ◽  
Frank L. Hanley

Purpose: Children with congenital heart disease may present with severe airway compression prior to any surgical procedure or may develop airway compression following their surgical procedure. This combination of congenital heart defect and airway compression poses a significant management challenge. The purpose of this study was to review our experience with the Lecompte procedure for relief of severe airway compression. Methods: This was a retrospective review of ten patients who underwent a Lecompte procedure for relief of severe airway compression over the past nine years (2010-2018). Three patients with absent pulmonary valve syndrome presented with severe symptoms prior to any surgical procedure. Seven patients presented with symptoms of airway compression following repair of their congenital heart defects (one with absent pulmonary valve syndrome, three patients had repair of pulmonary atresia with ventricular septal defect, and three patients had undergone aortic arch surgery). The median age at presentation was two years (range: one day to seven years). Results: The ten patients underwent a Lecompte procedure without any significant complications or operative mortality. The median interval between the surgical procedure and extubation was 9.5 days. No patients have required any further interventions for relief of airway obstruction. Conclusions: The Lecompte procedure is a surgical option for young children who present with severe airway compression. The patients in this series responded well to the Lecompte procedure as evidenced by clinical relief of airway compression.



2004 ◽  
Vol 43 (4) ◽  
pp. 216-218
Author(s):  
Cheng-Shing Kuo ◽  
Kok-Min Seow ◽  
Jiann-Loung Hwang ◽  
Gong-Jhe Wu


2016 ◽  
Vol 5 ◽  
pp. 15-18
Author(s):  
Tyler D. Robinson ◽  
Matias Bruzoni ◽  
Peter Than ◽  
Safwan Halabi ◽  
James Wall


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