Posttraumatic Cranial Cystic Fibrous Dysplasia

Tomiyama, Arata; Aoki, Kosuke; Nakayama, Haruo; Izukura, Hideaki; Kimura, Hitoshi; Harashina, Junichi; Ito, Keisuke; Hayashi, Morito; Saito, Norihiko; Sakurai, Takatoshi; Oharaseki, Toshiaki; Terada, Hitoshi; Iwabuchi, Satoshi

doi:10.1155/2011/680401

Cited by 5 publications

(3 citation statements)

References 6 publications

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“…A position correlation between increase in c-fos gene and FD was described by Marie et al [ 22 ]. Increase in c-fos gene has been related to post-traumatic FD in a couple of case reports[ 23 , 24 ]. Therefore, to avoid the risk of transforming a quiescent lesion into an aggressively growing lesion, we planned to proceed with sequential orthodontic tooth movement, using light forces, without applying any direct forces to the bone (through micro-implants) and to monitor the lesion periodically.…”

Section: Discussionmentioning

confidence: 99%

Comprehensive management of malocclusion in maxillary fibrous dysplasia: A case report

Kaur¹,

Mohanty²,

Kochhar³

et al. 2021

WJCC

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BACKGROUND Fibrous dysplasia (FD) is a developmental hamartomatous bone disease characterized by a blend of fibrous and osseous entities. Though rarely malignant, the tumor can vary from being small and asymptomatic, to a fairly large sized lesion, progressing gradually, compromising occlusion and facial esthetics. Treatment approach depends on the stage of skeletal maturity. It primarily involves surgical management for stabilizing the disease process. Post-surgical comprehensive dental treatment is necessary for restoring form and function of the jaws and teeth. This article describes comprehensive orthodontic management of severe malocclusion in a surgically operated case of FD maxilla. CASE SUMMARY A 19-year female presented with a chief complaint of excessive gingival display when smiling. Dental history included swelling of gums around the upper right front teeth, diagnosed at the age of 15 as FD of the right anterior maxillary segment and treated with surgical recontouring of the dysplastic bone. The clinical and radiological examinations showed adequate post-surgical healing. The surgically treated dysplastic area presented with right canting of the maxillary anterior occlusal plane. The maxillary teeth were torqued palatally, with the root of the right maxillary canine exposed clinically. We discuss sequential management of the associated malocclusion with comprehensive fixed orthodontics, along with special precautions taken to prevent reactivation of the quiescent and healed lesion. CONCLUSION The adequate healing of fibro-dysplastic bone post-surgery must be allowed before initiating orthodontic tooth movement in the dysplastic bone. Periodic follow-ups are needed to monitor stability of occlusion and any relapse of the lesion.

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Section: Discussionmentioning

confidence: 99%

Comprehensive management of malocclusion in maxillary fibrous dysplasia: A case report

Kaur¹,

Mohanty²,

Kochhar³

et al. 2021

WJCC

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“…The patient we report in this article is a very rare case for the localization of fibrous dysplasia. In the literature, there is a total of seven occipital fibrous dysplasia cases reported ( Table 1 ) [ 11 – 17 ].…”

Section: Discussionmentioning

confidence: 99%

Monostotic fibrous dysplasia involving occipital bone: a case report and review of literature

Başaran¹,

Kaksi²,

Gür³

et al. 2014

Pan Afr Med J

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Fibrous dysplasia (FD) is a progressive systemic bone tumour of young and it can be seen on cranial bones. FD is divided into three types according to radiological features. The second most common subtype is polyostotic subtype. With this article, we aimed to review and present clinical features, radiological examination, differential diagnosis and treatment management of a case of solitary monostotic fibrous dysplasia of occipital bone. 15 years old female patient admitted to our hospital for a bump and in the back of his head that she noticed 1 month ago. Her physical and neurological examination was normal. On cranial CT examination we detected a bony defect. Her gadolinium enhanced cranial MRI revealed bony defect along with massive gadolinium enhancement in adjacent tissue. On histopathologic examination; PANCK, CD68, CD1a were found negative and CD45, S-100, Vimentine were found positive. Ki-67 was 4,8%. In conclusion, fibrous dysplasia is a progressive bone disease of the young patients. Despite its resemblance to a benign lesion by not being symptomatic it can progress and cause severe bony defects and skin lesions. Total surgical resection is necessary and sufficient for total treatment.

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“…After exhaustive literature review, we consider this to be the second case of a posttraumatic cranial FD to the best of our knowledge. [ 4 ]…”

Section: Introductionmentioning

confidence: 99%

Post-traumatic fibrous dysplasia of the parietal bone: A rare entity

et al. 2017

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Fibrous dysplasia (FD) is a rare fibro-osseous lesion in which normal bone is replaced by abnormal fibrous tissue. Although a congenital disorder, a single case report of traumatic etiology had been described in the literature. We report a case of monostotic FD of the parietal calvarium in a 21-year-old female patient who presented to us with a single swelling in the parietal region been noticed after head injury sustained at the age of 7 years. After imaging investigations, the lesion was excised via craniotomy followed by cranioplasty in the same sitting. The histopathological evidence was suggestive of FD. To the best of our knowledge, this is the second case of a posttraumatic cranial FD and the first case describing the growing mass in the parietal bone secondary to head injury.

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Posttraumatic Cranial Cystic Fibrous Dysplasia

Cited by 5 publications

References 6 publications

Comprehensive management of malocclusion in maxillary fibrous dysplasia: A case report

Comprehensive management of malocclusion in maxillary fibrous dysplasia: A case report

Monostotic fibrous dysplasia involving occipital bone: a case report and review of literature

Post-traumatic fibrous dysplasia of the parietal bone: A rare entity

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