scholarly journals Epidural cerebrospinal fluid collection following lumbar puncture in an adult patient: A case report and literature review

2018 ◽  
Vol 9 (1) ◽  
pp. 169 ◽  
Author(s):  
Edward Monaco III ◽  
Jonathon Cavaleri ◽  
JenniferL Perez ◽  
Alp Ozpinar ◽  
Nima Alan
2010 ◽  
Vol 125 (3) ◽  
pp. 321-323
Author(s):  
C Kirton ◽  
A Guidera

AbstractObjective:We present an unusual case of parapharyngeal cerebrospinal fluid collection causing upper airway obstruction following a temporal bone fracture.Method:Case report and literature review of temporal bone fracture associated with parapharyngeal cerebrospinal fluid collection.Results:A 19-year-old man presented with cerebrospinal fluid otorrhoea and temporal bone fracture following a head injury. He was discharged after 48 hours of observation. The patient returned within 6 hours with sudden unilateral neck swelling and stridor after blowing his nose. Flexible nasendoscopy and computed tomography showed extrinsic compression of the pharynx, with partial upper airway obstruction. A literature review using Pubmed™ and Medline™ identified no previously reported cases of parapharyngeal cerebrospinal fluid collection associated with temporal bone fracture.Conclusion:This case illustrates a previously undescribed complication of temporal bone fracture. Raised intracranial pressure in the presence of a cerebrospinal fluid fistula may lead to airway obstruction, following temporal bone fracture.


2021 ◽  
Vol 103 (2) ◽  
pp. e74-e75
Author(s):  
M Flatman ◽  
Z Harb

We present a case of bilateral anterior superior iliac spine avulsion fractures in an adult patient who was involved in a road traffic collision. Her injuries were managed conservatively and she has had an uncomplicated recovery with a good outcome. This is, to our knowledge, the only reported case of bilateral simultaneous anterior superior iliac spine apophyseal avulsion fractures in an adult.


Author(s):  
Alberto Consolaro ◽  
Eduardo Sant'Ana ◽  
Melaine A. Lawall ◽  
Maria Fernanda M.O. Consolaro ◽  
Carlos Eduardo Bacchi

2018 ◽  
Vol 82 (1) ◽  
pp. 86
Author(s):  
O. I. Sharipov ◽  
M. A. Kutin ◽  
A. V. Bayuklin ◽  
A. A. Imaev ◽  
A. A. Abdilatipov ◽  
...  

2009 ◽  
Vol 25 (7) ◽  
pp. 467-468 ◽  
Author(s):  
Paul L. Aronson ◽  
Mark R. Zonfrillo

2016 ◽  
Vol 20 ◽  
pp. 60-62 ◽  
Author(s):  
Ilyas Dolas ◽  
Hasan Ogunc Apaydin ◽  
Seyho Cem Yucetas ◽  
Mehmet Davut Ucar ◽  
Suleyman Kilinc ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Sarah Nelson

The syndrome of transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis (HaNDL syndrome) is a self-limited condition. Confusional states are uncommonly reported as a clinical manifestation of this syndrome. Here, I report a 76-year-old female who presented with headache, confusion, and agitation with a mild CSF lymphocytosis. Other workup to determine the cause of her altered mental status was otherwise negative. The literature available in the English language on HaNDL syndrome is reviewed, including its history, pathophysiology, possible associations with migraine and stroke, and previously reported cases of confusional states in this syndrome. While HaNDL syndrome has been a described entity since the 1980s, its pathophysiology has yet to be clearly defined.


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