ea0049ep345 | Endocrine tumours and neoplasia | ECE2017
Mamedova Elizaveta
, Mokrysheva Natalya
, Vasilyev Evgeny
, Voronkova Iya
, Orlova Elizaveta
, Kareva Maria
, Belaya Zhanna
, Rozhinskaya Liudmila
, Tiulpakov Anatoly
Introduction: Hyperparathyroidism-jaw tumour syndrome (HPT-JT) is a rare disorder, which is frequently characterized by the development of parathyroid carcinomas and atypical parathyroid adenomas and, thus, severe course of primary hyperparathyroidism (PHPT).Case reports: Two patients (1 male and 1 female, 18 y.o. and 13 y.o. at the time of diagnosis of PHPT, respectively) among a cohort of young patients (<40 y.o.) with PHPT, underwent next...