Craniofacial fibrous dysplasia (CFD) of the maxilla in an 11-year old boy: a case report.
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Craniofacial fibrous dysplasia (CFD) of the maxilla in an 11-year old boy: a case report. / Assaf, Alexandre; Benecke, Andreas W.; Riecke, Björn; Zustin, Jozef; Fuhrmann, Andreas; Heiland, Max; Friedrich, Reinhard.
in: J CRANIO MAXILL SURG, Jahrgang 40, Nr. 8, 8, 01.12.2012, S. 788-792.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Craniofacial fibrous dysplasia (CFD) of the maxilla in an 11-year old boy: a case report.
AU - Assaf, Alexandre
AU - Benecke, Andreas W.
AU - Riecke, Björn
AU - Zustin, Jozef
AU - Fuhrmann, Andreas
AU - Heiland, Max
AU - Friedrich, Reinhard
N1 - Copyright © 2012 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
PY - 2012/12/1
Y1 - 2012/12/1
N2 - We present the case of a surgically treated 11-year old boy with a diagnosis of craniomaxillofacial fibrous dysplasia (CFD) in the maxillary sinus. When first seen in the outpatient clinic of our department he had minimal symptoms. After initial radiological diagnostics by computed tomography scans (CT-scans) the patient was treated operatively by radical excision of the tumor. The radiographs showed the typical intramedullary located and well-defined lesions, which eroded the cortical bone with the typical appearance of fibrous dysplasia. The histopathology showed the typical curved extending fibrous trabeculae in C, O and Y-shape which were embedded in a moderately cellular morphologically inconspicuous stroma, confirming the initial suspicion of fibrous dysplasia of the maxillary bone. Cone beam tomography was a valuable tool in determining the re-ossification of bone at the affected side. Local resection can be curative in limited disease.
AB - We present the case of a surgically treated 11-year old boy with a diagnosis of craniomaxillofacial fibrous dysplasia (CFD) in the maxillary sinus. When first seen in the outpatient clinic of our department he had minimal symptoms. After initial radiological diagnostics by computed tomography scans (CT-scans) the patient was treated operatively by radical excision of the tumor. The radiographs showed the typical intramedullary located and well-defined lesions, which eroded the cortical bone with the typical appearance of fibrous dysplasia. The histopathology showed the typical curved extending fibrous trabeculae in C, O and Y-shape which were embedded in a moderately cellular morphologically inconspicuous stroma, confirming the initial suspicion of fibrous dysplasia of the maxillary bone. Cone beam tomography was a valuable tool in determining the re-ossification of bone at the affected side. Local resection can be curative in limited disease.
KW - Humans
KW - Male
KW - Child
KW - Follow-Up Studies
KW - Tomography, X-Ray Computed/methods
KW - Osteogenesis/physiology
KW - Cone-Beam Computed Tomography/methods
KW - Fibrous Dysplasia of Bone/diagnosis/surgery
KW - Maxillary Diseases/diagnosis/surgery
KW - Maxillary Sinus/pathology
KW - Humans
KW - Male
KW - Child
KW - Follow-Up Studies
KW - Tomography, X-Ray Computed/methods
KW - Osteogenesis/physiology
KW - Cone-Beam Computed Tomography/methods
KW - Fibrous Dysplasia of Bone/diagnosis/surgery
KW - Maxillary Diseases/diagnosis/surgery
KW - Maxillary Sinus/pathology
U2 - 10.1016/j.jcms.2012.02.016
DO - 10.1016/j.jcms.2012.02.016
M3 - SCORING: Journal article
C2 - 22436487
VL - 40
SP - 788
EP - 792
JO - J CRANIO MAXILL SURG
JF - J CRANIO MAXILL SURG
SN - 1010-5182
IS - 8
M1 - 8
ER -
