scholarly journals Case report: Undetected retained orbital wood fragment mimicking orbital cellulitis

2021 ◽  
Vol 2 ◽  
pp. 100044
Author(s):  
Helen Katsarelis ◽  
Segun Awotesu ◽  
Tristan Mcmullan ◽  
Philip Ameerally
2017 ◽  
Vol 25 (1) ◽  
pp. 48
Author(s):  
AdebayoA Ibikunle ◽  
OlanrewajuA Taiwo ◽  
RamatO Braimah

2017 ◽  
Vol 2 (1) ◽  
pp. 49-54
Author(s):  
MA Akinola ◽  
AO Betiku ◽  
AP Adefalujo ◽  
AOA Yusuf ◽  
AO Sorungbe ◽  
...  

Objective: The aim of this report is to demonstrate that acute rhino-sinusitis may result in orbital cellulitis and even life threatening complications especially intracranial abscesses in children and young adults. Rare complications such as subperiosteal abscess seen in this patient may also occur Morbidity and mortality can be prevented through early diagnosis and treatment by relevant specialists. Method: We present a case report and literature review on unilateral pansinusitis complicated with orbital cellulitis and subperiosteal abscess of the frontal bone. Results: Following a diagnosis of orbital cellulitis and subperiosteal abscess of the frontal bone from a unilateral pansinusitis, an initial intravenous antibiotic was given for 72 hours, followed by a surgical drainage with subsequent rapid improvement. Conclusion: Acute rhinosinusitis may be complicated by orbital cellulitis and abscess formation. Prompt referral to a tertiary health facility as well as ooperation between the Ophthalmologists and Otorhinolaryngologists is very important to prevent life threatening complications. Key words: Orbital cellulitis, Pansinusitis, Subperiosteal abscess


Orbit ◽  
2008 ◽  
Vol 27 (4) ◽  
pp. 309-312 ◽  
Author(s):  
H. Mohammed J. Hassan ◽  
Philip T. Mc Andrew ◽  
Ali Yagan ◽  
Thomas S. Jacques ◽  
Richard Hayward

Author(s):  
M. Gabriela del Valle González-Cannata ◽  
Alfredo Medina-Zarco ◽  
Diana I. González-Hinojosa ◽  
Karla J. Aguilera-Ruiz ◽  
Martha P. González-Núñez ◽  
...  

2017 ◽  
Vol 5 (2) ◽  
pp. 1465-1468
Author(s):  
Dr.Fatimaal. mulhim ◽  
◽  
Dr Anoudal jamaan ◽  
Dr. kauser ◽  
Dr.Abdulmohsinal mulhim ◽  
...  

PEDIATRICS ◽  
1977 ◽  
Vol 59 (6) ◽  
pp. 1053-1054
Author(s):  
Kenneth C. Henderson ◽  
Reuben S. Roberts ◽  
Susan B. Dorsey

Group B β-hemolytic streptococci have gained much attention in recent years as a cause of serious infection in the newborn. Two clinical syndromes have been defined as "early onset" fulminant septicemia and a "late onset" meningitis.1,2 Howard and McCracken,3 more recently, have documented some previously unrecognized clinical presentations of group B streptococcal disease. These include asymptomatic bacteremia, septic arthritis, osteomyelitis, ethmoiditis with orbital cellulitis, pneumonia with empyema, facial cellulitis, and conjunctivitis. The literature to date reports five instances of osteomyelitis due to group B streptococci as reported in four articles.3-6 This case report of group B streptococcal osteomyelitis is presented to emphasize the insidious nature of this infection in a neonate and the lack of systemic toxicity with which it occurs.


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