A case report of a patient with parathyroid carcinoma and a CDC73 germline mutation

Author(s):  
Nuno Raposo ◽  
Nadia Bala ◽  
Sonia Pratas ◽  
Cristina Valadas
Author(s):  
Monica Serrano-Gonzalez ◽  
Sophie Shay ◽  
Juliana Austin ◽  
Dennis R. Maceri ◽  
Pisit Pitukcheewanont

AbstractParathyroid carcinoma is a rare cause of primary hyperparathyroidism amongst children, with only nine previously reported cases. The objective of the study was to present the first pediatric case with a germline


2021 ◽  
pp. 102571
Author(s):  
Zainab Lajmi ◽  
Ahlem Bdioui ◽  
Ahlem Bchir ◽  
Oussama belkacem ◽  
Emene Ben Ammou ◽  
...  

1981 ◽  
Vol 282 (2) ◽  
pp. 80-84 ◽  
Author(s):  
A. Philippe Chahinian ◽  
James F. Holland ◽  
Herbert E. Nieburgs ◽  
Ana Marinescu ◽  
Stephen A. Geller ◽  
...  

Hip & Pelvis ◽  
2016 ◽  
Vol 28 (3) ◽  
pp. 173 ◽  
Author(s):  
Sang-Hyun Park ◽  
Gyu-Min Kong ◽  
Yong-Uk Kwon ◽  
Jun-Ho Park

Author(s):  
Muzaffer Ilhan ◽  
İskender Ekinci ◽  
Özcan Karaman ◽  
Seda Turgut ◽  
Ertuğrul Taşan

2021 ◽  
Author(s):  
Rashid Rushdina Sofia Abdul ◽  
Abilash Sathyanarayanan ◽  
Ali Hisham Elhag ◽  
Antonia Ugur

2019 ◽  
Author(s):  
Anna C Beck ◽  
Sonia L Sugg

The clinical presentation and genetic mutations associated with parathyroid cancer are reviewed. Surgery, other treatment modalities, and outcomes are discussed. This review contains 1 table and 19 references. Key Words: CDC73-related parathyroid carcinoma, denosumab, HRPT2 germline mutation, hyperparthyroidism-jaw tumor syndrome, parathyroid carcinoma


Head & Neck ◽  
2015 ◽  
Vol 37 (11) ◽  
pp. E139-E141 ◽  
Author(s):  
James K. Fortson ◽  
Roger Su ◽  
Vijaykumar G. Patel ◽  
Gillian E. Lawrence

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