Page 195 - Abstract Book KONIKA 18
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Endocrinology

                                              P-ENDO-037
                    Delayed Puberty in A Girl as A Rare Sign of Craniopharyngioma

                             Andina Nirmala Pahalawati, Ismi Citra Ismail, Frida Soesanti
             Department of Child Health, Faculty of Medicine, Universitas Indonesia /Dr. Cipto Mangunkusumo General Hospital,
                                             Jakarta, Indonesia
                                               Abstract
            Background Craniopharyngiomas are the most frequently encountered suprasellar tumours in children.
            To date, hypopituitarism leading to a delayed puberty is a rare presentation of craniopharyngioma.
            Objective To present a case of a 17-year-old girl with short stature and delayed puberty as a rare presentation
            of craniopharyngioma. Case A 17 year-old-girl was referred from district hospital due to short stature and
            delayed puberty. The genitalia were feminine having no ambiguity. She was a bright girl without mental
            retardation. The patient was 135 cm in height and weight 24 kg. The parents was concern about her height
            since she was 12 years old because she was the shortest in class. Local pediatrician referred her to nearest
            obstetrician and gynecologist that stated it was normal since she had uterus from USG examination. At the
            age of 16 years old, the menses have not been occured nor the sign of secondary sexual characteristics.
            Another obstetrician and gynecologyst done another USG examination and said she has a small uterus and
            refer her to endocrinologist as she saw her short stature. She felt severe headache, blurry vision, and repeated
            vomiting for the last month. She came at our emergency unit with dehydration due to profuse vomiting. The
            funduscopy examination showed no optic disk edema. The laboratory findings showed hypogonadotropic
            hypogonadism, hypotirodism, and hypoprolactin (panhypopituitarism) leading to suspicion of brain tumor.
            The patient had an MRI of the brain confirming definitive diagnosis of Craniopharyngioma and preoperative
            planning. Brain tumor removal was done sucessfully without any sequele. The patient is in good condition,
            undergo radiotherapy session for the remaining tumor. Conclusions Craniopharyngioma should be considered
            in diagnosing patients with signs of hypopituitarism including delayed puberty and short stature.
                         Keywords: delayed puberty; craniopharyngioma; short stature; hypopituitarism


                                              P-ENDO-038
                             Effect of Thiamazole on Body Weight Changes
              in Children with Grave’s Disease at H. Adam Malik General Hospital Medan
                 Zakirin, Karina Sugih Arto, Tina Christina Lumban Tobing, Melda Deliana, Siska Mayasari Lubis
              Department of Child Health, Faculty of Medicine Universitas Sumatera Utara/Haji Adam Malik General Hospital
                                       Medan, North Sumatera, Indonesia
                                               Abstract
            Background Grave’s disease is the most common cause of hyperthyroidism in children and adolescents.
            Thyroid hormones are involved in metabolic regulation and influenced nutritional status. Many studies found
            the increment of body weight after Thiamazole treatment. Objective To evaluate change in body weight,
            nutritional status, and thyroid profile  after treatment of Thiamazole. Methods A cohort retrospective study
            was performed from January 2018 until December 2020. Subject was patients with Grave’s Disease. Weight,
            nutritional status and thyroid profile on 3 months after treatment and 6 months after treatment was recorded
            on medical record. Patient with incomplete data was excluded.Results There were 32 patients. Majority of
            subjects was girl (n=30, 93.8%) aged 6.6–17.4 years old. Patients presented in normal weight (n=11), obesity
            (n=8), moderate malnutrition (n=7), overweight (n=5) and severe malnutrition (n=1). The increase of body
            weight (3.7; 95%CI 3 to 4.4 kg), height (0.5; 95%CI 0.2 to 0.8 cm), body mass index (1.6; 95%CI 1. to 2
            kg/m ) after 6 months treatment (P<0.01). There was a statistical significance of nutritional status improvement
                2
            after 6 months (P<0.01). Increment of body weight was significance based on nutritional status (P<0.05).
            Changes of FT4 level was also significant (1.6; 95%CI 1.1 to 2.1 µg/dL; P<0.01) and TSH level was not
            significant (P=0.075) Conclusion Treatment of Thiamazole increased body weight and nutritional status in
            patients. Therefore, educational nutrition and long-term follow up should be performed.
                              Keywords: pediatric; Grave’s disease; thiamazole; body weight






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