Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep1026 | Pituitary - Clinical | ECE2017

Pituitary insufficiency following traumatic thoracic injury in adolescent male patient-case study

Gilis-Januszewska Aleksandra , Wilusz Malgorzata , Turek-Jabrocka Renata , Pantoflinski Jacek , Trofimiuk-Muldner Malgorzata , Kluczynski Lukasz , Hubalewska-Dydejczyk Alicja , Pach Dorota

Traumatic thoracic injuries in children and adolescents are rare, but could be connected with others traumas, often with traumatic brain injury (TBI). Based on data in the current literature, approximately 15–20% of TBI patients develop chronic hypopituitarism. Growth hormone (GH) and ACTH deficiency are the most common, followed by gonadotropins and thyroid-stimulating hormone. The greatest challenge associated with endocrine complications in individuals with polytrauma ...

ea0041ep300 | Clinical case reports - Pituitary/Adrenal | ECE2016

Temozolomide treatment in pituitary tumor causing Cushing’s Disease resistant to conventional therapy – case report

Gilis-Januszewska Aleksandra , Pantoflinski Jacek , Turek-Jabrocka Renata , Sokolowski Grzegorz , Wilusz Malgorzata , Pach Dorota , Hubalewska-Dydejczyk Alicja

Objective: The management of pituitary tumors causing Cushing’s Disease are a multidisciplinary challenge to clinicians with neurosurgery as a first line treatment followed by the radiotherapy and pharmacotherapy including chemiotherapy.Such tumors are difficult to treat with high rate of recurrence. To date only 25 patients with Cushing Disease treated with the new alkylating agent temozolamide (TMZ) have been reported.Materials and methods: Sixty-...

ea0056gp125 | Endocrine Case Reports | ECE2018

Hyperinsulinaemic hypoglycaemia in the three generations of a family with GCK, c.295T>C (p.Trp99Arg) mutation

Gilis-Januszewska Aleksandra , Skalniak Anna , Wilusz Malgorzata , Sokolowski Grzegorz , Walczyk Joanna , Pantoflinski Jacek , Pach Dorota , Przybylik-Mazurek Elwira , Hubalewska-Dydejczyk Alicja

Background: Familial Hyperinsulinaemic hypoglycaemia (FHH) is a very rare disease with heterogeneous clinical manifestation causing risk of late diagnosis or even misdiagnosis. In infants and children, it can lead to serious and permanent damage to the central nervous system. FHH has been correlated with mono-gene mutations in approximately 48% of cases. Clinical manifestation may vary even in the same affected GCK mutation family.Objective: To describe ...

ea0056p1072 | Thyroid (non-cancer) | ECE2018

Iodine deficiency in pregnancy – is the situation in poland improving?

Trofimiuk-Muldner Malgorzata , Sokolowski Grzegorz , Konopka Joanna , Dubiel Agnieszka , Kiec-Klimczak Malgorzata , Kluczynski Lukasz , Motyka Marcin , Rzepka Ewelina , Stefanska Agnieszka , Walczyk Joanna , Wilusz Malgorzata , Lewinski Andrzej , Zygmunt Arkadiusz , Pach Dorota , Hubalewska-Dydejczyk Alicja

Iodine deficiency is considered the most common preventable cause of brain damage worldwide. It is particularly important during pregnancy, as it influences not only mothers but their fetuses as well. The Polish model of iodine prophylaxis is based on obligatory household salt iodization and recommendation of iodine-containing supplements for pregnant women. The aim of the study was to assess the current iodine status of pregnant women and to compare it with earlier results.</...