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Bilateral Brachial Plexopathy Complicating Henoch-Schonlein Purpura

dc.authorscopusid 8421729700
dc.authorscopusid 7101974609
dc.authorscopusid 7006604555
dc.authorscopusid 6701642517
dc.authorscopusid 6603968029
dc.authorscopusid 56336609600
dc.authorscopusid 56336609600
dc.authorwosid Arslan, Şükrü/Abc-4250-2021
dc.authorwosid Odabaş, Dursun/Mbh-2762-2025
dc.contributor.author Yilmaz, C
dc.contributor.author Çaksen, H
dc.contributor.author Arslan, S
dc.contributor.author Anlar, Ö
dc.contributor.author Atas, B
dc.contributor.author Güven, AS
dc.contributor.author Odabas, D
dc.date.accessioned 2025-05-10T17:29:17Z
dc.date.available 2025-05-10T17:29:17Z
dc.date.issued 2006
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Yuzuncu Yil Univ, Dept Pediat Neurol, Fac Med, Van, Turkey; Yuzuncu Yil Univ, Fac Med, Dept Neurol, Van, Turkey en_US
dc.description.abstract An 11-year-old boy presented with convulsion, fever, rash, abdominal pain, swelling on the eyelids, elbow and wrists, oliguria and hematuria. Based on the abnormal findings the patient was diagnosed with Henoch-Schonlein purpura. On the 3rd day of admission, neurological examination showed ataxic gait, loss of deep tendon reflexes, and decreased (4/5) of muscle strength on all extremities. Additionally, bilateral loss of touch, pain and temperature sensation in a glove, from the elbows to distal region (on C5-T1 level) was diagnosed. Cerebrospinal fluid examination and cranial magnetic resonance imaging (MRI) were normal. The patient was discharged with oral prednisolone on the 7th day of admission. One week after discharging from the hospital, he was re-admitted with vertigo and seizures. He was in coma. MRI of cranial, cervical and cervical plexus were normal. Electromyography showed severe bilateral brachial plexopathy. Prednisolone and intravenous immunglobulin (IVIG) therapy were given without significant improvement. He was discharged from the hospital on the 17th day of admission. On the second month of follow-up, a second cure of IVIG was given because of no clinical improvement. Now, he is on the 4th month of follow-up, unfortunately, no improvement was noted on his muscle strength and sensorial abnormalities on the upper extremities. (c) 2006 Elsevier B.V. All rights reserved. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1016/j.braindev.2005.09.007
dc.identifier.endpage 328 en_US
dc.identifier.issn 0387-7604
dc.identifier.issue 5 en_US
dc.identifier.pmid 16376046
dc.identifier.scopus 2-s2.0-33745885426
dc.identifier.scopusquality Q3
dc.identifier.startpage 326 en_US
dc.identifier.uri https://doi.org/10.1016/j.braindev.2005.09.007
dc.identifier.uri https://hdl.handle.net/20.500.14720/12303
dc.identifier.volume 28 en_US
dc.identifier.wos WOS:000237542000010
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Elsevier Science Bv 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 Brachial Plexopathy en_US
dc.subject Child en_US
dc.subject Henoch-Schonlein Purpura en_US
dc.title Bilateral Brachial Plexopathy Complicating Henoch-Schonlein Purpura en_US
dc.type Article en_US

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