Page 342 - Abstract Book KONIKA 18
P. 342

Neurology

                                              P-NEU-011
                 Spondylitis Tuberculosis in Adolescent with Disseminated Tuberculosis:
                                            A Case Report

                                Pebriansyah, Setyo Handryastuti, Nastiti Kaswandani
                Department of Child Health, Faculty of Medicine, Universitas Indonesia/Dr. Cipto Mangunkusumo Hospital,
                                             Jakarta, Indonesia

                                               Abstract
            Background  Spondylitis tuberculosis is one of the most common extrapulmonary tuberculosis following
            disseminated tuberculosis. Clinical manifestations are heterogeneous and insidious. If left untreated, it could
            lead into severe neurological deficits resulting poor quality of life and became a national burden in the future.
            Objective To demonstrate diagnostic approach and comprehensive management of spondylitis tuberculosis
            in adolescent with disseminated tuberculosis. Case A 16-year-old boy was admitted with a chief complaint
            of abdominal distention and back pain two weeks before admission. Following months, he was kyphotic,
            paralyzed and numb in both legs, and incapable of urination. The patient had enlargement of lymph nodes
            (3.5x3.5 cm) on the neck and had been ruptured five months ago, mild pain and bent of the backbone, and
            loss significant bodyweight. No history of trauma or tuberculosis in the family. On physical examination, he
            was parestesis and paraplegia in both lower extremities, sclofuroderma was already dried and necrotic, and
            kyphotic and gibbus formation around posterior thoracalis. Supportive examinations found destruction and
            fusion resulting moderate spondylolisthesis, abscess with kyphotic formation, multiple tuberculoma in the
            brain, and bilateral reticulonodular infiltrate suggestive tuberculosis of the lung. Managements consisted of
            anti-tuberculous agent and surgery. Conclusion There are several variations in systemic and also neurologic
            symptoms in spondylitis tuberculosis patient. The prognosis influenced by the patient’s age, the severity
            of kyphosis deformity, the amount of vertebrae involvement, the site of the lesion and the patient’s health
            status, such as nutritional status and other comorbidities.
                           Keywords: adolescen; spondylitis tuberculosis; disseminated tuberculosis


                                              P-NEU-012
              Risk Factors of Epilepsy and Generalized Epilepsy with Febrile Seizures Plus
                 associated with Systemic Complications and Developmental Disorders:
                                            A Case Report

                                        Egi Azhar Rafsanjani, Irwanto
                       Klinik Sabil, Departement of Child Health, Faculty of Medicine Universitas Airlangga,
                                         Surabaya, East Java, Indonesia

                                               Abstract
            Background Epilepsy has various risk factors. Each of these risk factors increases the incidence of epilepsy
            by 4%-6% while the combination of these risk factors will increase the incidence of epilepsy by 10%-49%.
            There are about 10-20% of people with epilepsy will experience at least one episode of status epilepticus
            which can cause systemic complications and possible future complications such as developmental disorders.
            Objective To show the connection between the risk factors of epilepsy and the incidence of generalized
            epilepsy with febrile seizures plus (GEFS+) in relation to its future complications. Case An 8-year-old boy
            came to the hospital after experiencing a seizure during fever. He had first history of febrile seizures at the
            age of 3 months and at the age of 4 years he had a seizure without fever and started taking anti-epileptic
            drugs. He had a history of ventriculoperitoneal shunt procedures due to hydrocephalus. He has cerebral
            palsy and global developmental delay. On physical examination, there was atrophy and hypotonia on the
            right and left legs. His brother also have epilepsy. General management of epilepsy has shown good clinical
            results in this case. Conclusion It is important to find out the cause of seizures in epilepsy and GEFS+ to
            avoid systemic complications.
                   Keywords:  developmental disorder; epilepsy; GEFS+; risk factors of epilepsy; status epilepticus







            294                           KONIKA XVIII Abstract Book
   337   338   339   340   341   342   343   344   345   346   347