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dc.contributor.authorBebek, Nerses
dc.contributor.authorEmre, Murat
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorYesilot, Nilüfer
dc.contributor.authorKurtuncu, MURAT
dc.contributor.authorGurses, Candan
dc.contributor.authorJirsch, Jeffrey
dc.contributor.authorGokyigit, Aysen
dc.contributor.authorAndermann, Frederick
dc.contributor.authorBaykan, BETÜL
dc.date.accessioned2021-03-04T18:09:27Z
dc.date.available2021-03-04T18:09:27Z
dc.date.issued2007
dc.identifier.citationGurses C., Kurtuncu M., Jirsch J., Yesilot N., Hanagasi H. A. , Bebek N., Baykan B., Emre M., Gokyigit A., Andermann F., "Neurosyphilis presenting with status epilepticus", EPILEPTIC DISORDERS, cilt.9, ss.51-56, 2007
dc.identifier.issn1294-9361
dc.identifier.otherav_8938a58a-fb8e-46cd-bec3-ee74d26606bb
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/93070
dc.identifier.urihttps://doi.org/10.1684/epd.2007.0058
dc.description.abstractThree patients with neurosyphilis are reported. The first and third patients presented with convulsive status epilepticus and the second with non-convulsive status after penicillin administration. in all cerebrospinal fluid and the serum Venereal Disease Research Laboratory Test (VDRL) and Treponema Pallidum hemagglutination (TPHA) or fluorescent treponemal antibody absorption test (FTA-ABS) were positive, but HIV serology was negative. Their EEGs showed periodic, lateralized, epileptiform discharges (PLEDs) just after SE. The first and third patients had no history of epilepsy. Seizures started as focal motor attacks but then secondarily generalized. The first patient's cranial MRI showed cerebral atrophy and hyperintensity involving bilateral medial and anterior temporal regions, more prominent on the left and which disappeared after penicillin treatment. The second case, after receiving penicillin, had nonconvulsive SE, a clinical presentation suggesting a Jarisch-Herxheimer reaction (JHR). Her cranial MR revealed moderate cortical atrophy and widespread confluent hyperintense foci mainly in both periventricular areas, corona radiata and centrum semiovale. MRI of the third case showed a large, left sylvian, arachnoid cyst without mass effect. Executive dysfunction was observed in follow-up neuropsychological tests in all patients. When investigating status epilepticus, neurosyphilis as a cause must not be forgotten.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeurosyphilis presenting with status epilepticus
dc.typeMakale
dc.relation.journalEPILEPTIC DISORDERS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume9
dc.identifier.issue1
dc.identifier.startpage51
dc.identifier.endpage56
dc.contributor.firstauthorID60777


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