hrp0095p1-408 | Adrenals and HPA Axis | ESPE2022

Diverse clinical features, genetic etiologies, and histopathological features of adrenal neoplasms in children and adolescents

Choi Yunha , Hwang Soojin , Kim Gu-Hwan , Yoo Han-Wook , Choi Jin-Ho

Purpose: Adrenal neoplasms (ANs) are rare endocrine neoplasms in children, and etiopathogenesis and prognosis of pediatric ANs remain obscure. This study investigated clinical features, histopathological features, genetic etiologies and prognosis of ANs.Methods: This study included 33 ANs patients diagnosed from March 1997 to April 2021. Clinical features and endocrine findings were collected by retrospective medical cha...

hrp0098t5 | Top 20 Posters | ESPE2024

Endocrine and metabolic complications after solid organ transplantation in childhood and adolescents

Yoon Ji-Hee , Kim Dohyung , Hwang Soojin , Hye Kim Ja , Choi Jin-Ho

Context: Acute or chronic metabolic derangement after solid organ transplantation (SOT) can result in endocrine complications. As survival rates following SOT have significantly increased, the occurrence of endocrine complications has also risen.Objective: This study was performed to investigate long-term endocrine complications after SOT in children and adolescents.Methods: This s...

hrp0097p1-338 | Multisystem Endocrine Disorders | ESPE2023

Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents

Yoon Ji-Hee , Choi Yunha , Hwang Soojin , Lee Yena , Hye Kim Ja , Choi Jin-Ho , Yoo Han-Wook

Purpose: As the survival rate for pediatric cancers increases significantly with advances in treatment modalities, long-term endocrine complications have also risen. This study investigated the frequencies and risks of endocrine sequelae of childhood cancer survivors after hematopoietic stem cell transplantation (HSCT).Methods: This study included 200 pediatric patients who underwent HSCT. Clinical and endocrinological f...

hrp0097p2-96 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2023

Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes

Yoon Ji-Hee , Lee Nae-Yun , Hye Kim Ja , Hwang Soojin , Kim Gu-Hwan , Yoo Han-Wook , Choi Jin-Ho

Purpose: Androgen insensitivity syndrome (AIS) is a rare X-linked recessive disorder caused by unresponsiveness to androgen because of mutations in the AR gene. Here, we investigated the clinical outcomes and molecular spectrum of AR variants in patients with AIS attending a single academic center.Methods: This study included 19 patients with AIS who were confirmed by molecular analysis of AR. Clinical features and endoc...