Craniofacial polyossal fibrous dysplasia

Author:

Kulakova G. A.1ORCID,Solovyeva N. A.1ORCID,Kurmaeva E. A.1ORCID,Volgina S. Ya.1ORCID,Nikiforova E. V.2ORCID,Davletshina G. I.1ORCID,Kuptsova D. O.1ORCID

Affiliation:

1. Kazan State Medical University

2. Children’s Polyclinic No. 10

Abstract

Fibrous dysplasia is a rare anomaly of bone tissue development, in which it is replaced by fibrocystic tissue. A clinical case of a patient with a craniofacial polyossal form of fibrous dysplasia is presented. At the age of 13, a child had a constant intense headache, which was accompanied by dizziness, tinnitus, cognitive impairment, deformity of the frontal region and lower jaw on the right, local pigmentation in the neck and face (coffee-and-milk-like stains). Brain tomography and osteoscintigraphy visualized a volumetric formation in the right half of the skull bones, in which fibrotic dysplasia was revealed during histological examination.Conclusion. To establish this diagnosis, a combination of pain syndrome with deformation of the facial part of the skull and histological examination is important. 

Publisher

The National Academy of Pediatric Science and Innovation

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

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