Page 350 - Abstract Book KONIKA 18
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Neurology

                                              P-NEU-027
                       Case Report: Guillain-Barré Syndrome in 4-year-old Child

                                     Nurichwani Wardianda, Johanus Edwin
                               Bunda Aliyah Mother and Child Hospital, Jakarta, Indonesia

                                               Abstract
            Background Guillain-Barré syndrome or acute idiopathic polyradiculoneuritis is a rare and serious immune-
            mediated peripheral neuropathic disorder. It is frequently preceded by an unspecified infection and has a
            characteristic symptoms such as areflexia, flaccidity and symmetrical ascending weakness. This syndrome
            is much rarer in children and adolescents, with an incidence of 0.62 cases per 100,000 person years in 0-9
            year olds.  Objective To improve the early recognition and diagnosis of Gullain-Barré Syndrome in children.
            Case A 4-year-old male patient was brought to the hospital due to abdominal pain for a week. The patient
            also complained of diarrhoea for one day before admission. Other symptoms such as fever, vomiting, cough
            were not found. On the fourth day of hospitalisation, the patient felt weakness in both legs and ascended
            to arms. The patient began to speak incoherently and choked while drinking. The patient was transferred
            to the PICU due to difficulty breathing and was put on a ventilator. On the physical examination, there was
            flaccidity, hyporeflexia, and decreased motor strength in the lower extremity that ascended to the upper
            extremity. There was no significant abnormality in the laboratory result. The patient was given oxygen
            supplementation by a ventilator, IVIG, and crystalloid fluid. After the third day of using IVIG, there was
            a slight improvement of motor strength at the right lower extremity and response for communication. The
            patient was hospitalized for 7 days and then referred to RSCM. Conclusion Although rare, it’s important to
            recognize the variety and severity of the neurological symptoms of GBS in children.
                                    Keywords: Guillain-Barré syndrome; children


                                              P-NEU-028
              Improvement of Multiple Bacterial Brain Abscess in Child Following Abscesses
                      Aspiration and Administration of Antibiotics: A Case Report

                                         Irwan Santoso, Agung Triono
                 Departement of Child Health, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/
                          Dr. Sardjito Hospital, Special District of Yogyakarta, Central Java, Indonesia
                                               Abstract
            Background Childhood brain abscess is a rare focal infection of the brain that begins as a localized area of
            cerebritis and often involving patients with specific risk factors. Bacteria are responsible for >95% of brain
            abscesses through hematogenous dissemination following cyanotic heart disease (26%) and contiguous spread
            following otogenic infection (25%). Treatment of brain abscess requires a combination of antimicrobials
            and surgical intervention. Objective To demonstrate a long-term outcome of a child with multiple brain
            abscesses after antibiotics and surgical intervention. Case An eighteen-month-old male was referred from
            a private hospital with cranial nerve palsy and altered consciousness due to meningoencephalitis. Three
            weeks prior, the patient had fever, vomiting, and purulent ear discharge. Two days prior he had frequent
            vomiting, oculomotor and facial nerve palsy, and altered consciousness. He was then hospitalized in a private
            hospital for two days, but no clinical improvement thus referred to our hospital. His initial PCS was 13 and
            neurological examination shown cranial nerve palsy and right hemiparesis. Laboratory studies revealed
            leucocyte 21.010/ µL with neutrophil 76,8% and contrast head CT revealed multiple hypodense lesions
            with rim enhancement and midline shifting. We administered intracranial dose cefotaxime, dexamethasone,
            and mannitol. The neurosurgeon performed abscess aspiration three times at two weeks intervals. Abscess
            fluid culture revealed chains cocci – Streptococci. The patient became compos mentis and cranial nerve
            became normal after the first aspiration. On the 55  day of hospitalization, he was discharged with normal
                                                 th
            consciousness and cranial nerve but right hemiparesis persisted. One year after the first aspiration, contrast
            head CT revealed no brain abscess.  Conclusion Altered consciousness, cranial nerve palsy and hemiparesis
            can be caused by brain abscess from child with specific risk factors. Combination of neurosurgery and
            adequate antibiotic made prognosis better.
                           Keywords: brain abscess; abscess aspiration; intracranial dose antibiotics



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