Recurrent Juvenile Psammomatoid Ossifying Fibroma with Secondary Aneurysmal Bone Cyst of the Maxilla: A Case Report and Review of Literature

Sarode, Sachin C.; Sarode, Gargi S; Ingale, Yashwant; Ingale, Manjusha; Majumdar, Barnali; Patil, Nilesh; Patil, Shankargouda

doi:10.4081/cp.2018.1085

Cited by 17 publications

(11 citation statements)

References 13 publications

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“…The mean age of occurrence JPSOF is approximately 20 years whereas in case of JTOF, the mean age of occurence is 81/2 to 12 years suggesting JTOF is more common in children and adolescents. In the current case the patient was 15 yrs considering the age of the patient it is more in favour of JTOF however literature review ( 8 , 9 ) reports that JPSOF have been observed in patients as young as three months and as old as seventy two years and the present case is a classic example of this wide age range of JPSOF as the patient was 15yrs which is the age more common for JTOF.…”

Section: Discussionmentioning

confidence: 55%

Juvenile psammomatoid ossifying fibroma of Orbit-A rare case report and review of literature

Kamalakaran¹,

Bharathi²,

Thirunavukkarasu³

2021

J Clin Exp Dent

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Fibro osseous lesions of the craniofacial skeleton are a benign condition in which the normal architecture of the bone is replaced by fibrous connective tissue with varying degrees of mineralization. JOF forms a special entity among the fibro osseous lesions because of its age of occurrence and its aggressive nature thereby mimicking a malignancy. The Juvenile Ossifying Fibromas were further subdivided into Psammomatoid and Trabecular variant based on their histopathological characteristics. They tend to differ in their mineralized portion with the trabecular variant showing woven bone while the psammamotoid shows lamellated and spherical ossicles in various shapes in a myxoid stroma intermingled with bone cyst like areas. The reported cases of JPSOF are few, hence histopathological examination is a valuable tool in the diagnosis of this rare lesion and JOF should always be considered in the differential diagnosis of the lesions of the craniofacial skeleton. Early diagnosis and a complete surgical excision with adequate margins and a long term follow up is mandatory for a good prognosis of this highly recurrent and aggressive lesion.The diagnosis of JOF requires a careful correlation of clinical, radiological and histopathological features. The purpose of this paper is to report a case of JPOF of the orbit to stress the need for consideration of JOF in the differential diagnosis of the aggressive lesions of the Cranio facial skeleton. Key words: Juvenile psammomatoid ossifying fibroma, orbit, ossifying fibroma.

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Section: Discussionmentioning

confidence: 55%

Juvenile psammomatoid ossifying fibroma of Orbit-A rare case report and review of literature

Kamalakaran¹,

Bharathi²,

Thirunavukkarasu³

2021

J Clin Exp Dent

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“…FD, OF, and cementoosseous dysplasia are the noted BFOLs. [14] e recent World Health Organization classification of head and neck tumors in 2017 described four fibro-osseous lesions: OF, FD, familial gigantiform cementoma (FGC), and cemento-osseous dysplasia. [2,5,8,9,13] OFs are benign fibro-osseous neoplasms affecting the craniofacial skeleton.…”

Section: Discussionmentioning

confidence: 99%

Orbit ossifying fibroma – Case report and literature review

Rabelo

Silva

Santo

et al. 2020

Surgical Neurology International

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Background: Ossifying fibroma (OF) is benign bone lesions, most frequent in young children, more common in the maxillary sinus and mandible (75–89%), the pathogenesis of the tumor is not clear, there are many subtypes of OF. This paper aims to report an OF a case and literature review. Case Description: Male, 19 years old, with a progressive history proptosis since 2012, diagnosed as a right supraorbital lesion at an external service and assigned to conservative management. Then, he evolved with double vision, which worsened in February of 2018, associated with a moderate headache. On admission: proptosis and downward deviation of the right orbit was noticed on the physical exam and with exception of limited right upgaze, external ocular movements were maintained. Head computed tomography showed a multiloculate expansive osteolytic lesion at the right orbital roof. On magnetic resonance imaging, the lesion had an inner content with septations, T1-weighted imaging heterogeneous signal, T2-weighted imaging high signal intensity, and peripheral contrast enhancement. The patient underwent a right frontal craniotomy with a gross total resection and the postoperative follow-up was uneventful. Menzel reported the first case in 1782. The clinical findings depend on localization. There are five subtypes. In general, the lesions have a radiological appearance with hyperdense boundary and cause deformity and destruction in bones with high recurrence risk. Radical resection is curative. Conclusion: As a result, the correlation of clinical, radiologic, and pathologic data is significant while going for a specific diagnosis in cases of craniofacial fibrous lesions. Total excision is the best treatment, but it can recur.

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“…Simple curettage or excision will not disconnect the blood supply nor correct the displacement of vessels which logically leads to a second expansion. Pedwa et al ( 17 ), Trent et al ( 13 ), Sarode et al ( 32 ) and Gotmare et al ( 33 ) all reported JABCs with initial curettage treatment then followed by recurrence and a second thorough hemi-mandibulectomy or maxillectomy were needed. Reddy et al ( 25 ) also presented a relapse case in which this patient had taken over a second curettage along with cryotherapy.…”

Section: Discussionmentioning

confidence: 99%

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

2021

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In the past half-century, considerable attention has been paid to oral and maxillofacial skeletal cyst, however, aneurysmal bone cyst (ABC), unlike other common bone diseases, still contours numerous unanswered questions in terms of classification, etiology and pathological mechanism. The purpose of this article was to evaluate the proportion of primary ABC and secondary ABC, and to assess the recurrence of ABC and related factors. A methodical search of Embase, MEDLINE, Cochrane Library, Web of Science was conducted for well-documented jaw aneurysmal bone cyst (JABC) cases. One hundred thirty-one articles were identified after database searching and 31 of them were included in our study for further research with 44 JABC cases. All the articles were analyzed by two separate authors. About 25% of the reported jaw aneurysmal bone cyst was secondary. Both the pathological classification and surgical treatment had a significant influence on recurrence rate (P = 0.0082, P = 0.0022), while patients' age or radiographic features rarely affected prognosis. Jaw aneurysmal bone cysts can present variable clinical and histological presentations. Recurrence may be attributed to omittance of underlying potential blood supply or conservative surgical protocol.

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Recurrent Juvenile Psammomatoid Ossifying Fibroma with Secondary Aneurysmal Bone Cyst of the Maxilla: A Case Report and Review of Literature

Cited by 17 publications

References 13 publications

Juvenile psammomatoid ossifying fibroma of Orbit-A rare case report and review of literature

Juvenile psammomatoid ossifying fibroma of Orbit-A rare case report and review of literature

Orbit ossifying fibroma – Case report and literature review

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

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