Searchable abstracts of presentations at key conferences in endocrinology

ea0090p34 | Calcium and Bone | ECE2023

Two cases of parathyromatosis in patients with recurrent primary hyperparathyroidism

Matejkova Behanova Magdalena , Libansky Petr , Vaculova Marketa , Chmelova Renata , Personova Kateřina , Vcelak Josef , Vlcek Petr

Introduction: Parathyromatosis is a rare cause of recurrent hyperparathyroidism defined as small nodules of hyperfunctioning parathyroid tissue in the soft tissues of the neck or mediastinum. The most common cause is probably the implantation of parathyroid cells into surrounding tissue during surgery and the risk of parathyromatosis increases with repeated parathyroid surgery. There is an overlap in the histologic features in parathyromatosis, atypical adenoma, and parathyroi...

ea0090p596 | Calcium and Bone | ECE2023

Surgery of primary hyperparathyroidism during pregnancy: case series

Libansky Petr , Fialova Martina , Jezkova Jana , Kosak Mikulas , Matejkova Behanova Magdalena , Moravcova Jitka , Vcelak Josef , Vaculova Marketa , Lischke Robert

Background: Primary hyperparathyroidism can occur at any age, the typical patient is a postmenopausal woman, primary hyperparathyroidsim is found rare by pregnant women. The maternal symptoms are similar to the symptoms by postmenopausal women.Materials and methods: Among the years 2000-2022 we have performed 3459 operations (including 6,6% reoperations) with diagnosis of hyperparathyroidism, there were six women, who underwent parathyroidectomy during p...

ea0081p294 | Calcium and Bone | ECE2022

Genetic testing in patients with primary hyperparathyroidism before surgery

Matejkova Behanova Magdalena , Vcelak Josef , Moravcova Jitka , Personova Katerřina , Vaculova Marketa , Chmelova Renata , Junkova Kristyna , Ježkova Jana , Fialova Martina , Libansky Petr

Introduction: Familial and hereditary forms of primary hyperparathyroidism (PHPT) represent a small minority of all patients with PHPT (5 – 10%). The surgical approach is different in such cases than in sporadic PHPT. Hereditary PHPT may be syndromic (multiple endocrine neoplasia: MEN – type 1, 2A or 4 and others) or nonsyndromic (familial isolated PHPT). The aim of the study was to identify and describe hereditary and familial forms of PHPT in patients referred to p...