scholarly journals Screw Migration into Colon after Anterior Cervical Plating - An Unusual Complication: A Case Report

2020 ◽  
Vol 14 (3) ◽  
pp. 184-187
Author(s):  
Sath S

2008 ◽  
Vol 89 (3) ◽  
pp. 564-567 ◽  
Author(s):  
Su-Ra Ryu ◽  
Jae-Hyung Kim ◽  
In-Sung Choi ◽  
Jae-Young Han ◽  
Sam-Gyu Lee


Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
pp. 7077 ◽  
Author(s):  
Panagiotis Katsinelos ◽  
Ioannis Pilpilidis ◽  
Grigoris Chatzimavroudis ◽  
Taxiarchis Katsinelos ◽  
Georgia Lazaraki ◽  
...  




Cureus ◽  
2021 ◽  
Author(s):  
Saumya Agrawal ◽  
Bhargav Gajula ◽  
Anil Kumar Chongtham ◽  
Farhanul Huda ◽  
Somprakas Basu


BDJ ◽  
2006 ◽  
Vol 200 (11) ◽  
pp. 614-615
Author(s):  
E Mein ◽  
S K D Lewis ◽  
J Mein


2018 ◽  
Vol 9 ◽  
pp. 215145851875779
Author(s):  
Rayan Fairag ◽  
Fahad H. Abduljabbar ◽  
Alex Page ◽  
Ron Dimentberg

Intramedullary nailing is the mainstay of treatment for unstable intertrochanteric hip fractures. Various complications have been described with the use of these nails. We report an unusual complication whereby the lag screw completely missed the nail. We hypothesize that this previously unreported complication may be related to a specific flexible carbon fiber aiming device. Surgeon awareness and thorough intraoperative imaging are crucial to avoiding this complication.



2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Sebastian Schwab ◽  
Simon Lissmann ◽  
Niklas Schäfer ◽  
Alexander Isaak ◽  
Dietrich Klingmüller ◽  
...  

Abstract Background The clinical features, course and outcome of hantavirus infection is highly variable. Symptoms of the central nervous system may occur, but often present atypically and diagnostically challenging. Even though the incidence of hantavirus infection is increasing worldwide, this case is the first to describe diabetes insipidus centralis as a complication of hantavirus infection in the Western world. Case presentation A 49-year old male presenting with severe headache, nausea and photophobia to our neurology department was diagnosed with acute haemorrhage in the pituitary gland by magnetic resonance imaging. In the following days, the patient developed severe oliguric acute kidney failure. Diagnostic workup revealed a hantavirus infection, so that the pituitary haemorrhage resulting in hypopituitarism was seen as a consequence of hantavirus-induced hypophysitis. Under hormone replacement and symptomatic therapy, the patient’s condition and kidney function improved considerably, but significant polyuria persisted, which was initially attributed to recovery from kidney injury. However, water deprivation test revealed central diabetes insipidus, indicating involvement of the posterior pituitary gland. The amount of urine production normalized with desmopressin substitution. Conclusion Our case report highlights that neurological complications of hantavirus infection should be considered in patients with atypical clinical presentation.



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