presentamos un caso de displasia fibrosa monostótica localizada en el seno entre ellos el síndrome de albright (sólo en casos de displasia poliostótica). su. Displasia fibrosa monostótica e poliostótica. Front Cover. Simone Paula Bibliographic information. QR code for Displasia fibrosa monostótica e poliostótica. Download PDF. 1 / 3 Pages. Previous article. Go back to website. Next article.
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Dental characteristics of fibrous dysplasia and McCune-Albright syndrome. Female patient aged 10 years old ;oliostotica referred to the radiology department for CBCT examination to investigate a painless hard oedema on the left side of the maxilla with unknown evolution and absence of painful symptoms.
Fibrous displasia: Report three cases
According to Lisle et al. Other syndrome less common than polyostotic FD may be associated with Mazabraud syndrome, which is characterised by the involvement of soft tissues with presence of intra-muscular myxomas 511 – 1216 The recurrent behavior of Fibrous Dysplasia is essential to its surgical planning and it was also analyzed on this study.
The objective of this study was to report the cone beam computed tomography CBCT results of a case of monostotic FD in the maxilla and discuss on the importance of image exams for diagnosis of this lesion.
Services on Demand Journal. However, in the majority of the cases, the unpolished glass appearance was the most prevalent image 8 FD is a rare but potentially severe disease which can cause fracture when affecting long bones, including osseous pain, deformities and compression of surrounding tissues 17.
In the present case, one of the teeth affected by the lesion was under orthodontic traction. Services on Demand Journal.
Juiz de Fora, MG, Brasil. The purpose of this study is to make a review of the main clinical, radiological poliosotica histopathological findings that contributes to the differential diagnosis. FD is frequently found in children and young adults 617such as in the present case of a female year-old patient. The surgical treatment of fibrous dysplasia.
Fibrous dysplasia is a benign fibrous-osseous dissplasia in which normal bone is replaced by fibrous connective tissue and immature bone, affecting only one monostotic or several bones polyostotic and mainly occurring in children and young adults.
According to Akintoye et al.
Although some studies reported the indication of magnetic resonance imaging MRI for diagnosis of FD 62026this type of examination does not reveal the distinctive characteristic of FD as observed in radiographs and Diisplasia images 6820since the lesion may often be confounded with tumours 68.
Fibrous dysplasia FD is a rare benign fibro-osseous lesion 1 – 7 characterised by the gradual replacement of the normal bone by fibrous tissue and immature bone 58.
Moreover, CT can be used to complement the diagnosis and improve the interpretation of MRI examinations of lesions in the bones of skull base and face, since the appearance of unpolished glass will confirm the diagnosis of FD. This is due to the fact that the imaging aspects of FD are very distinctive. The differential diagnosis of FD includes osteomyelitis, osteosarcoma 17 and cemento-ossifying fibroma 1317 – En bloc resection and bone graft: In this type of FD, man and women are affected with the same frequency 712 – 13 In general, the lesion begins in fibtosa childhood and progresses during monoztotica, ceasing after adolescence 4.
J Oral Maxillofac Surg. All of them had recurrences after surgical removal, diagnosed between first and eighth year monosttoica follow up.
Monostotic fibrous dysplasia: a case report with cone-beam computed tomography findings
Computed tomography is the ideal method for evaluating this lesion and its relationship with adjacent structures. Craniofacial fibrous dysplasia of the fronto-orbital region: Nevertheless, in those cases of mild deformity as in the present caseit is recommended to follow up the lesion by performing imaging examinations on a poliototica basis until skeletal maturity, since relapse is very common following surgical treatment 1 In this way, CT is a definitive examination for early diagnosis, surgery planning and follow-up of patients.
When FD reaches the sphenoid, temporal, zygomatic and frontal-nasal bones of the maxilla and skull base is termed as craniofacial FD 1811 – 12 Int J Oral Maxillofac Surg.
Unilateral blindness after ipsilateral prophylactic transcranial optic canal decompression for fibrous dysplasia.
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In the image exams, the main characteristic of fibrous dysplasia is its unpolished glass appearance. It is worth emphasising that the initial lesions are more radiolucent, becoming more poliostotuca as the lesion develops 16 One can observe slight prominence in the anterior and posterior regions of the left maxilla and monostoticq tooth 21 with presence of orthodontic wire for traction.
All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Ossifying fibroma involving the paranasal sinuses, orbit, and anterior cranial fossa: Due to the unpolished glass appearance of FD on the images 13the imaging diagnosis is enough and thus bone biopsy is firbosa necessary 8 Craniofacial and monostotic variants of fibrous dysplasia affecting themaxillofacial.
CT imaging of craniofacial fibrous dysplasia.