Overview of the 2022 WHO classification of familial endocrine tumor syndromes

V Nosé, A Gill, JMC Teijeiro, A Perren, L Erickson - Endocrine pathology, 2022 - Springer
This review of the familial tumor syndromes involving the endocrine organs is focused on
discussing the main updates on the upcoming fifth edition of the WHO Classification of …

Molecular genetics of syndromic and non‐syndromic forms of parathyroid carcinoma

L Cardoso, M Stevenson, RV Thakker - Human mutation, 2017 - Wiley Online Library
Parathyroid carcinoma (PC) may occur as part of a complex hereditary syndrome or an
isolated (ie, non‐syndromic) non‐hereditary (ie, sporadic) endocrinopathy. Studies of …

Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism‐jaw tumor syndrome (HPT‐JT) and parathyroid tumors

PJ Newey, MR Bowl, T Cranston… - Human mutation, 2010 - Wiley Online Library
The hyperparathyroidism‐jaw tumor (HPT‐JT) syndrome is an autosomal dominant disorder
characterized by the occurrence of parathyroid tumors in association with ossifying fibromas …

[HTML][HTML] Ossifying fibroma vs fibrous dysplasia of the jaw: molecular and immunological characterization

S Toyosawa, M Yuki, M Kishino, Y Ogawa, T Ueda… - Modern Pathology, 2007 - Elsevier
Ossifying fibroma and fibrous dysplasia of the jaw are maxillofacial fibro-osseous lesions
that should be distinguished each other by a pathologist because they show distinct patterns …

Fibro-osseous lesions of the craniofacial skeleton: an update

SK El-Mofty - Head and neck pathology, 2014 - Springer
Benign fibro-osseous lesions of the craniofacial skeleton (BFOL) are a variant group of
intraosseous disease processes that share similar microscopic features characterized by …

Molecular and clinical Spectrum of primary hyperparathyroidism

S Jha, WF Simonds - Endocrine Reviews, 2023 - academic.oup.com
Recent data suggest an increase in the overall incidence of parathyroid disorders, with
primary hyperparathyroidism (PHPT) being the most prevalent parathyroid disorder. PHPT is …

[HTML][HTML] Parathyroid cancer: A review

NN Machado, SM Wilhelm - Cancers, 2019 - mdpi.com
Parathyroid cancer is one of the rarest causes of primary hyperparathyroidism and tends to
present with more severe symptoms than its more benign counterparts. This article details …

[HTML][HTML] Oncogenic microRNA-155 down-regulates tumor suppressor CDC73 and promotes oral squamous cell carcinoma cell proliferation: implications for cancer …

MI Rather, MN Nagashri, SS Swamy… - Journal of Biological …, 2013 - ASBMB
The CDC73 gene is mutationally inactivated in hereditary and sporadic parathyroid tumors.
It negatively regulates β-catenin, cyclin D1, and c-MYC. Down-regulation of CDC73 has …

Juvenile psammomatoid ossifying fibroma: a review

SC Sarode, GS Sarode, P Waknis, A Patil, M Jashika - Oral oncology, 2011 - Elsevier
In WHO classification of odontogenic tumors (2005), juvenile ossifying fibroma (JOF) is
divided into juvenile psammomatoid ossifying fibroma (JPOF) and juvenile trabecular …

Phenotypic profiling and molecular mechanisms in hyperparathyroidism-jaw tumor syndrome

R Tora, J Welch, J Sun, SK Agarwal… - The Journal of …, 2023 - academic.oup.com
Context Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a heritable form of primary
hyperparathyroidism caused by germline inactivating mutations in CDC73 encoding …