Segmental odontomaxillary dysplasia

Authors

DOI:

https://doi.org/10.60094/RID.20230101-22

Keywords:

Bone diseases developmental, maxilla, dentofacial deformities, tooth abnormalities, diagnostic imaging

Abstract

Segmental  odontomaxillary  dysplasia  (SOMD)  is  a  rare  and  non-inherited  developmental pathology  characterized  by  the  variability  of  its  clinical  and  radiological  characteristics  and  can  mimic other fibro-osseous lesions. Clinically, it is diagnosed by a unilateral deformation of the maxilla,  ipsilateral  gingival  enlargement  and  agenesis  of  one  or  two  premolars.  We  report  a  case  of SOMD in a 21-year-old male patient, who presented facial asymmetry of the left middle third, hypopigmentation  of  the  left  upper  lip  with  discontinuity  in  the  vermilion  border  presenting  a  blurred  commissure,  orbital  hypertrichosis  on  the  left  side;  in  addition,  the  buccopalatal  volume  increase  of  the  left  upper  maxilla  and  an  abnormal  eruption  pattern.  The  radiographic  images  showed the bone trabeculae in a vertical position without showing a boundary between the lamina dura and the medullary bone. Being a rare entity, we will analyze the most up-to-date information available in the literature.

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References

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Published

2023-06-29

How to Cite

Cuenca de Figueroa, M. T. V., Calderón Ubaqui, V., Merino Bustamante, C. D., & Gonzales Pablo, C. R. (2023). Segmental odontomaxillary dysplasia. Reporte Imagenológico Dentomaxilofacial, 2(1), e2023020103. https://doi.org/10.60094/RID.20230101-22