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    An 11-month-old Girl with High Fever
    (SLACK INC, 2009) Ercan, Tugba Erener; Ercan, Gokmen; Arpaozu, Muhsin
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    Can high volume pericapsular nerve group (PENG) block act as a lumbar plexus block?
    (ELSEVIER SCIENCE INC, 2020) Alasehir, Elcin Akduman; Ipek, Belkiz Ongen; Thomas, David Terence; Ercan, Tugba Erener; Sitar, Mustafa Erinc
    Can high volume pericapsular nerve group (PENG) block act as a lumbar plexus block?
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    Mycoplasma pneumoniae infection & obsessive-compulsive disease: A case report
    (SAGE PUBLICATIONS INC, 2008) Ercan, Tugba Erener; Ercan, Gokmen; Severge, Burcu; Arpaozu, Muhsin; Karasu, Gulten
    It has been demonstrated that obsessive-compulsive disease and/or tic syndromes in children may be triggered by an antecedent infection especially with group A beta-hemolytic streptococci, and this subgroup of children has been designated by the acronym PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections). Other infectious agents such as viruses and bacteria have also been reported to be associated with the acute onset or dramatic exacerbation of obsessive-compulsive disease or Tourette syndrome, and another acronym, PITAND (pediatric infection-triggered autoimmune neuropsychiatric disorder) has appeared in the literature. The involvement of other infectious agents such as Mycoplasma pneumoniae has been described in single case reports. We describe a case of a 5.5-year-old boy who suddenly developed obsessive-compulsive disease symptoms during a M. pneumoniae pneumonia. After treatment with oral clarithromycin, all his obsessive-compulsive disease symptoms disappeared. To our knowledge, this is the first report that shows the association between Mycoplasnw pneumoniae infection and obsessive-compulsive disease.
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    Spontaneous Intracranial Hypotension: A Case Report
    (SAGE PUBLICATIONS INC, 2008) Uysal, Serap; Albayram, Sait; Ercan, Tugba Erener
    Spontaneous intracranial hypotension is a rare syndrome of low ccrebrospinal fluid pressure due to spontaneous cerebrospinal fluid leaks. The main feature is orthostatic headache. We describe a case of spontaneous intracranial hypotension in a 5-year-old girl with a 1-month history of headache, sudden onset hearing loss, and ataxia. Magnetic resonance imaging (MRI) showed an enlargement of cervical venous plexus and lumbar puncture revealed a low opening pressure. Magnetic resonance myelography showed leakage of the contrast material at the level of the third and fourth lumbar vertebra. Bed rest and caffeine treatment yielded no resolution of symptoms. Following a lumbar epidural blood patch, her headache and ataxia resolved completely without any improvement in hearing. A second blood patch also yielded no effect on hearing. Spontaneous intracranial hypotension should be considered in the differential diagnosis of headache, also in the pediatric age group.