Page 227 - Abstract Book KONIKA 18
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Hemato-Oncology

                                               P-HO-003
                          A 5-year-old Girl with Stage 4 Malignant Melanoma

                              Aldila Vidya Ditha Arianti, Ariawan, Bambang Sudarmanto
               Department of Child Health, Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java, Indonesia

                                               Abstract
            Background Malignant melanoma (MM) is an uncommon type of childhood cancer. The incidence is
            approximately 1 of 1,000,000. Childhood melanoma is considered more prevalent in certain groups,
            such as patients with giant congenital nevi and xeroderma pigmentosum. The 5-year survivals were 14%.
            Objective We report on a case of stage IV malignant melanoma to address the clinical features of this disease
            and the treatment using dacarbazine (DTIC). Case A 5-year-old girl admitted due to the presence of malignant
            melanoma involving the dorsal, forehead, arm and legs. Biopsy in 2017 revealed a giant congenital nevi. The
            lesion was larger than 50 cm, observed in mostly the dorsal part of the body, which was partially covered
            by hair with irregular pigmentation. Biopsy in 2021 revealed a malignant melanoma. This year, the clinical
            features showed a development of lymph nodes enlargement at the axilla and inguinal, > 1 cm diameter,
            darkened lesion accompanied by pain in both of his extremities which made her unable to walk. So far,
            this was the first case of MM who managed to received 2 cycles of DTIC. Conclusion We should have an
            awareness of melanoma in children that have giant congenital nevi.
                             Keywords: malignant melanoma; treatment; dacarbazine; children


                                               P-HO-004
                 Effect of Deferiprone and Deferasirox in Alleviation of Oxidative Stress
                    and Hyperuricemia in Beta Thalassemia Major Pediatric Patients

                                                           1
                            Andreas Budi Wijaya , Wulandewi Marhaeni , Wivina Riza Devi 2
                                           1
                                                         2
               Department of Pediatrics and  Department of Clinical Pathology , Ulin General Hospital, Faculty of Medicine,
                               1
                           Universitas Lambung Mangkurat, Banjarmasin, South Borneo, Indonesia
                                               Abstract
            Background Oxidative stress in β-TM patients is associated with increased malondialdehyde (MDA)
            level and decreased superoxide dismutase (SOD) level. Hyperuricemia, which was noted in 58% of β-TM
            pediatric patients in Ulin Hospital, might be associated with body's response to reduce oxidative stress.
            Deferiprone and deferasirox, which used for iron overload treatment, suggest the potential of antioxidants
            Objective To evaluate the effect of deferiprone and deferasirox on oxidative stress parameter and uric acid
            serum in β-TM pediatric patients. Methods Eighty seven β-TM patients (aged 2-≤18 years old) with iron
            chelators (deferiprone or deferasirox) and regular transfusion in Ulin Hospital between April-July 2019,
            were enrolled into this cohort study. They were followed up for 3 months. The laboratory investigations
            included complete blood count, ferritin, uric acid, MDA and SOD. Statistical analysis was used to compare
            ferritin, uric acid, MDA, and SOD before and after 3 months use of consecutive iron chelators agent.
            Results Subjects (n=87) from this study were 61% male and 39% female. Deferiprone was used by 74.7%
            patients. After being followed for 3 months, mean ferritin level of deferiprone group [3272.2 (SD 294.1)
            ng/mL] was significantly lower (P=0.018) than that of deferasirox group [4926.1 (SD 803.2) ng/mL). There
            was no significant difference in MDA, SOD and uric acid level between two groups. In comparison to
            baseline data, there was significant increase in SOD level (P=0.000) and decrease in uric acid (P=0.000),
            MDA (P=0.000) and ferritin level (P=0.000). Conclusion: Deferiprone and deferasirox can protect against
            oxidative stress and hyperuricemia in β-TM pediatric patients
                        Keywords: deferiprone; deferasirox; oxidative stress; hyperuricemia; thalassemia












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