PMID- 30045288 OWN - NLM STAT- MEDLINE DCOM- 20180802 LR - 20220419 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 97 IP - 30 DP - 2018 Jul TI - Increased intracranial pressure in Guillain-Barre syndrome: A case report. PG - e11584 LID - 10.1097/MD.0000000000011584 [doi] LID - e11584 AB - RATIONALE: Guillain-Barre syndrome (GBS) is an inflammatory autoimmune demyelinating polyneuropathy that affects most of the peripheral nervous system. Papilledema and raised intracranial pressure (ICP) are seen in some patients, and are thought to be associated with elevated cerebrospinal fluid (CSF) protein-though CSF protein levels are normal in some patients, thus the specific mechanisms remain unclear. Interleukin (IL)-17 levels are elevated in the CSF and plasma in GBS patients, and elevated IL-17 in the CSF of patients with idiopathic intracranial hypertension has been reported. Intravenous immunoglobulin (IVIG) exerts therapeutic effects by downregulating IL-17 in GBS patients. PATIENT CONCERNS: Herein we describe a case of a 14-year-old girl who initially presented with relapsing limb weakness. DIAGNOSES: Magnetic resonance imaging revealed an enlarged ventricle, electromyography, and nerve conduction studies were suggestive of polyradiculopathy, and lumbar puncture revealed elevated ICP with normal cells and elevated protein values. INTERVENTIONS: She was treated with IVIG 0.4 g/kg per day for 5 days. OUTCOMES: At a 6-month follow-up there had been no recurrence. LESSONS SUBSECTIONS: In GBS patients who have a relapsing course and develop papilledema with possible immunological disturbance, an accurate early diagnosis in conjunction with the prompt initiation of immunotherapy may improve clinical symptoms and the prognosis. FAU - Zhao, Pan-Pan AU - Zhao PP AD - Department of Neurology, First Affiliated Hospital of Xinxiang Medical University Henan Key Laboratory of Neural Regeneration Department of Neurosurgery, First Affiliated Hospital of Xinxiang Medical University, Weihui, China. FAU - Ji, Qian-Kun AU - Ji QK FAU - Sui, Rui-Bin AU - Sui RB FAU - Zhang, Rong AU - Zhang R FAU - Zhang, Li-Jun AU - Zhang LJ FAU - Xu, Zhi-Xiu AU - Xu ZX FAU - Li, Qing AU - Li Q FAU - Ji, Si-Bei AU - Ji SB FAU - Zhao, Jian-Hua AU - Zhao JH LA - eng PT - Case Reports PT - Journal Article PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (IL17A protein, human) RN - 0 (Immunoglobulins, Intravenous) RN - 0 (Immunologic Factors) RN - 0 (Interleukin-17) SB - IM MH - Adolescent MH - Female MH - Guillain-Barre Syndrome/*complications/drug therapy/immunology MH - Humans MH - Immunoglobulins, Intravenous/therapeutic use MH - Immunologic Factors/therapeutic use MH - Interleukin-17/blood MH - Intracranial Hypertension/drug therapy/*immunology MH - Muscle Weakness/drug therapy/*immunology PMC - PMC6078745 COIS- The authors have no conflicts of interest to disclose. EDAT- 2018/07/26 06:00 MHDA- 2018/08/03 06:00 PMCR- 2018/07/27 CRDT- 2018/07/26 06:00 PHST- 2018/07/26 06:00 [entrez] PHST- 2018/07/26 06:00 [pubmed] PHST- 2018/08/03 06:00 [medline] PHST- 2018/07/27 00:00 [pmc-release] AID - 00005792-201807270-00041 [pii] AID - MD-D-18-02167 [pii] AID - 10.1097/MD.0000000000011584 [doi] PST - ppublish SO - Medicine (Baltimore). 2018 Jul;97(30):e11584. doi: 10.1097/MD.0000000000011584.