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Cranio‐facial fibrous dysplasia in a 38‐year‐old African woman: a case history
Author(s) -
Simon E,
Matee M,
Shubi F,
Mselle T
Publication year - 1999
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/j.1601-0825.1999.tb00309.x
Subject(s) - maxilla , mandible (arthropod mouthpart) , fibrous dysplasia , medicine , anatomy , giant cell , dysplasia , pathology , biology , botany , genus
A 38–year‐old woman sought treatment with cranio‐facial dysplasia involving the cranium, maxilla and the mandible. Her chief complaint was a mandibular swelling, which had appeared about 2 years previously, had gradually enlarged, and was associated with spontaneous pain. X‐ray film examination revealed a ground‐glass opacity with blurred demarcation and a 99 Tc medronate bone scan disclosed an increase in tracer uptake in the cranium, maxilla and mandible. The rest of the skeleton was not affected. Histological examination of the lesions revealed solid proliferation of spindle‐shaped cells associated with islands of osteid and bone trabecullae with Chinese letter pattern and numerous multinucleated giant cells consistent with fibrous dysplasia. The continued osteoblastic activity of involved bones, coupled with the medical condition of the patient, restricted the management of the patient to largely supportive and palliative care.