scholarly journals Ventriculoperitoneal Shunt Disconnection Associated with Loss of Consciousness in a Child Patient: A Case Report and Review of Intra-Abdominal Complications of Vp Shunts

2017 ◽  
Vol 7 (2) ◽  
Author(s):  
Kaveh Haddadi
2010 ◽  
Vol 42 (4) ◽  
pp. 184-186 ◽  
Author(s):  
G. Ghidirim ◽  
I. Mishin ◽  
G. Zastavnitsky ◽  
V. Spataru ◽  
M. Brinza

Author(s):  
Raul-Ciprian Covrig ◽  
Jasmina Petridou ◽  
Ulrich J. Knappe

AbstractBrucellosis is a frequent zoonosis in some regions of the world and may cause various symptoms. Neurobrucellosis is a rare but serious complication of the infection. Our case report describes the course of neurobrucellosis in a patient who had received a ventriculoperitoneal shunt in his native country 13 years prior to diagnosis of brucellosis. He initially presented to us with symptoms of peritonitis, which misled us to perform abdominal surgery first. After the diagnosis of neurobrucellosis was confirmed and appropriate antibiotics were initiated, the symptoms soon disappeared. Although the ventriculoperitoneal shunt was subsequently removed, the patient did not develop a symptomatic hydrocephalus further on. This case displays the challenges in diagnosing an infection that occurred sporadically in Europe and may be missed by currently applied routine microbiological workup. Considering the political context, with increasing relocation from endemic areas to European countries, it is to be expected that the cases of brucellosis and neurobrucellosis will rise. Brucellosis should be considered and adequate investigations should be performed.


Author(s):  
Matthew T. Grant ◽  
Nicole A. Wilson ◽  
Martin S. Keller ◽  
Anna L. Huguenard ◽  
Jennifer M. Strahle ◽  
...  

Author(s):  
Yamila Nadia Itati Basilotta Márquez ◽  
Juan Pablo Mengide ◽  
Juan Manuel Liñares ◽  
Amparo Saenz ◽  
Romina Argañaraz ◽  
...  

Neurocirugía ◽  
2006 ◽  
Vol 17 (5) ◽  
pp. 450-452 ◽  
Author(s):  
M. Felipe-Murcia ◽  
M.J. Almagro ◽  
J.F. Martínez-Lage

1999 ◽  
Vol 39 (4) ◽  
pp. 313-315 ◽  
Author(s):  
M. Faik ÖZVEREN ◽  
Ahmet KAZEZ ◽  
Hasan ÇETIN ◽  
Ibrahim M. ZIYAL

2000 ◽  
Vol 54 (5) ◽  
pp. 388-396 ◽  
Author(s):  
Satish Sathyanarayana ◽  
Esther L Wylen ◽  
Mustafa K Baskaya ◽  
Anil Nanda

2021 ◽  
Vol 10 (2) ◽  
pp. e26610212430
Author(s):  
Gustavo Zanna Ferreira ◽  
Carolina Ferrairo Danieletto-Zanna ◽  
Liogi Iwaki Filho ◽  
Rômulo Maciel Lustosa ◽  
Willian Pecin Jacomacci ◽  
...  

The ameloblastic fibro-odontoma (AFO) is a mixed odontogenic tumor, with characteristics of ameloblastic fibroma, presenting enamel and dentin, which occurs more frequently in individuals aged 5 to 17 years. This paper reports na extensive case of ameloblastic fibro-odontoma in the mandible of a 3-year-old patient, discussed in comparison to cases selected from a brief literature review on the clinical characteristics, Evolution and therapeutic options for this lesion. In the last years, there was no consensus in the literature concerning its etiopathogenesis and classification, yet recently the AFO was classified as a developing odontoma. This case is in accordance with the 7 cases reported in the literature of AFO in the mandible of children aged 10 years or younger, especially concerning the lesion pattern and evolution and treatment adopted. The patient did not present relapse and exhibited local bone regeneration at the 3-year follow-up.


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