Successful treatment with therapeutic plasmapheresis of a pediatric patient with Guillain-Barré syndrome associated with neurobrucellosis
dc.authorid | Emine Manolya Kara / 0000-0001-6234-7024 | |
dc.authorscopusid | Emine Manolya Kara / 57905197200 | en_US |
dc.authorwosid | Emine Manolya Kara / CXW-4939-2022 | en_US |
dc.contributor.author | Varol, Fatih | |
dc.contributor.author | Yusuf Can, Yaşar | |
dc.contributor.author | Şahin, Ebru Güney | |
dc.contributor.author | Şahin, Süleyman Berkay | |
dc.contributor.author | Akyüz, Gülcan | |
dc.contributor.author | Aydın, Ali | |
dc.contributor.author | Kara, Emine Manolya | |
dc.contributor.author | Çam, Halit | |
dc.date.accessioned | 2022-11-07T06:45:47Z | |
dc.date.available | 2022-11-07T06:45:47Z | |
dc.date.issued | 2022 | en_US |
dc.department | İstinye Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.description.abstract | Brucellosis is a multisystemic disease that can present with multiple signs and symptoms. Rarely, brucellosis can manifest as neurobrucellosis, with central or peripheral nervous system involvement. Guillain-Barré syndrome (GBS) is a post-infectious autoimmune disease that progresses rapidly, causing ascending muscle weakness, and is accompanied by areflexia/hyporeflexia. Regarding GBS etiology, it is thought to be an autoimmune disease, triggered by a previous bacterial or viral infection. There are a few Brucella-associated GBS case reports in the literature and in our opinion, only one of them is a pediatric patient. Herein we reported a case of GBS associated with neurobrucellosis, who was successfully treated with therapeutic plasmapheresis (TP) due to poor response to IVIG treatment. | en_US |
dc.identifier.citation | Varol, F., Yusuf Can, Y., Sahin, E., Sahin, S. B., Akyuz, G., Aydin, A., . . . Cam, H. (2022). Successful treatment with therapeutic plasmapheresis of a pediatric patient with guillain-barré syndrome associated with neurobrucellosis. Journal of Clinical Apheresis, 37(5), 522-526. doi:10.1002/jca.22020 | en_US |
dc.identifier.doi | 10.1002/jca.22020 | en_US |
dc.identifier.endpage | 526 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.scopus | 2-s2.0-85138700393 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 522 | en_US |
dc.identifier.uri | https://doi.org/10.1002/jca.22020 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/3229 | |
dc.identifier.volume | 37 | en_US |
dc.identifier.wos | WOS:000857318300001 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Kara, Emine Manolya | |
dc.language.iso | en | en_US |
dc.publisher | John Wiley and Sons Inc | en_US |
dc.relation.ispartof | Journal of Clinical Apheresis | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Guillain-Barre | en_US |
dc.subject | Neurobrucellosis | en_US |
dc.subject | Plasma Exchange | en_US |
dc.title | Successful treatment with therapeutic plasmapheresis of a pediatric patient with Guillain-Barré syndrome associated with neurobrucellosis | en_US |
dc.type | Article | en_US |
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