Polyostotic Fibrous Dysplasia

Authors

  • Bessy Maldonado Third year resident of the Pediatrics Postgraduate Program at UNAH-VS
  • Lilian Dubón Third year resident of the Pediatrics Postgraduate Program at UNAH-VS
  • Tito Moreno Pediatric Care Physician at Hospital Mario Catarino Rivas, SPS, Honduras
  • Diana Ramírez Medical Specialist in Pediatric Oncology at Mario Catarino Rivas Hospital and Honduran Institute of Social Security

DOI:

https://doi.org/10.5377/pediatrica.v13i1.17596

Keywords:

fibrous dysplasia, bone tumor, bone biopsy

Abstract

Fibrous dysplasia (FD) or bone dysplasia is a rare bone development anomaly, with a frequency of between 5% and 7% of benign bone tumors, within these lesions, 50-70% are monostotic, 20-30% They are polyostotic and 3%-10% have McCune-Albright syndrome (DF, skin pigmentation and precocious puberty). It is characterized by the replacement of normal bone and bone marrow by fibrous tissue. A 15-year-old mixed-race male patient with a history of repeated fractures and bone deformity is presented. A diagnosis is established by imaging where lytic lesions are observed with a positive biopsy for FD. The condition has no specific treatment, its approach is multidisciplinary and represents a medical challenge.

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Abstract
40

Published

2024-02-26

How to Cite

Maldonado, B., Dubón, L., Moreno, T., & Ramírez, D. (2024). Polyostotic Fibrous Dysplasia. Acta Pediátrica Hondureña, 13(1). https://doi.org/10.5377/pediatrica.v13i1.17596