Searchable abstracts of presentations at key conferences in endocrinology

ea0011p938 | Thyroid | ECE2006

Impact of TNM classification categories on thyroid gland carcinoma

Sykorova P , Vlcek P , Jirsa L , Personova K

We have collected an extensive record of more than 8000 patients with a thyroid carcinoma over the years 1946–2005. In all cases, the diagnosis was done by the histology examination carried by a pathologist. Those records were classified by their dimension and the extent of the thyroid gland. This classification is used as a basis for the treatment decision. Tumors of the bigger size needs radiotherapy with I 131 whereas the smaller tumors are subject of observation and r...

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...

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...