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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Grigorie D, Sucaliuc A, Ciuffi S, Franceschelli F, Marini F, Ioachim D, Terzea D, Brandi ML
High Risk of Parathyroid Carcinoma and Genetic Screening in the First Diagnosed Romanian Family with Hyperparathyroidism-Jaw Tumor Syndrome and a Germline Mutation of the CDC73 Gene
Acta Endo (Buc) 2019, 15 (3): 398-403doi: 10.4183/aeb.2019.398
Context. Hyperparathyroidism-jaw tumour (HPTJT)
syndrome is a rare autosomal dominant cause of familial
hyperparathyroidism associated with ossifying fibromas (OF)
of the maxillofacial bones and increased risk of parathyroid
carcinoma, caused by inactivating germline mutation of the
cell division cycle 73 (CDC73) gene.
Objective. To report the first Romanian family
with HPT-JT and genetic screening of CDC73 gene.
Subjects and Methods. Mutational analysis of the
CDC73 gene and genetic screening of the family of a proband
with HPT-JT. Histological diagnosis of parathyroid tumors
(WHO criteria) and immunohistochemistry (parafibromin)
were performed.
Results. Three of the six screened family members
had evidence of PHPT and surgically proven parathyroid
tumours. Two of the three affected members had parathyroid
carcinomas and one had two parathyroid adenomas. Genetic
screening of CDC73 gene revealed that 4 of 6 patients
showed a heterozygous germline deletion of one nucleotide:
c.128-IVS1+1 delG. All the three affected patients, resulted
to be carriers of the CDC73 mutation, but each one bearing a
different CDC73 polymorphism.
Conclusions. We identified a new CDC73 germline
mutation in a Romanian family of HPT-JT. Analysis
of clinical phenotypes in the four mutated individuals
confirmed the incomplete penetrance and the variable
clinical expression of the disease.
Keywords: Familial Primary Hyperparathyroidism,
Parathyroid Carcinoma, HPT-JT, Germline CDC73 mutation,
Genetic screening.
Correspondence: Daniel Grigorie MD, PhD, Associate Professor of Endocrinology, “Carol Davila” University of Medicine and Pharmacy,
“C.I. Parhon” National Institute of Endocrinology, 34-38 Aviatorilor Blvd, Bucharest, 011863, Romania. E-mail: danielgrigorie58@gmail.com