Juvenile Trabecular Ossifying Fibroma (TrJOF) Orginating from Lateral Fronto-Orbital Bone with Secondary Aneurysmal Bone Cyst (ABC) Formation: Report of an Unusual Case and Literature Review

2021 ◽  
Vol 04 (03) ◽  
Author(s):  
Isra Abdalla ◽  
Ali Basalamah ◽  
Omar alwhaibi ◽  
Ammar Alrikabi ◽  
Ahmad Al Boukai ◽  
...  
Keyword(s):  
Literature Review ◽  
Aneurysmal Bone Cyst ◽  
Unusual Case ◽  
Bone Cyst ◽  
Ossifying Fibroma ◽  
Secondary Aneurysmal Bone Cyst

Classic Adamantinoma with Osteofibrous Dysplasia-like Foci and Secondary Aneurysmal Bone Cyst

2003 ◽  
Vol 6 (2) ◽  
pp. 173-178 ◽  
Author(s):  
Angelica Putnam ◽  
Suzanne Yandow ◽  
Cheryl M. Coffin
Keyword(s):  
Aneurysmal Bone Cyst ◽  
Unusual Case ◽  
Bone Cyst ◽  
Bone Lesion ◽  
Giant Cells ◽  
Multinucleated Giant Cells ◽  
Osteofibrous Dysplasia ◽  
Pathologic Features ◽  
History Of ◽  
Secondary Aneurysmal Bone Cyst

Adamantinoma, a rare bone lesion of the tibia and fibula, has two distinct variants, classic adamantinoma and osteofibrous dysplasia-like adamantinoma. Composite lesions have not been described. Aneurysmal bone cyst is a benign cystic lesion which may also occur in the tibia and fibula. We report an unusual case of classic adamantinoma with osteofibrous dysplasia-like areas and foci of secondary aneurysmal bone cyst with prominent giant cells. A lesion was diagnosed in a 17-year-old girl with a 14-year history of a slowly enlarging left tibial mass and increasing deformity. Pathologically, the predominant pattern was classic adamantinoma, with minor foci of osteofibrous dysplasia-like adamantinoma and areas of secondary aneurysmal bone cyst with abundant multinucleated giant cells. We report the clinical, radiologic, and pathologic features of this case, and summarize lesions associated with secondary aneurysmal bone cyst. To our knowledge, the association of adamantinoma with secondary aneurysmal bone cyst has not been previously reported.

Juvenile psammomatoid ossifying fibroma of the calcaneus

2020 ◽  
Vol 13 (8) ◽  
pp. e234555
Author(s):  
Rachel L Semus ◽  
Elizabeth Zielinski ◽  
William C Foster
Keyword(s):  
Unusual Case ◽  
Bone Cyst ◽  
Surgical Excision ◽  
Ossifying Fibroma ◽  
Early Management ◽  
Complete Surgical Excision ◽  
Odontogenic Origin ◽  
Secondary Aneurysmal Bone Cyst ◽  
Psammomatoid Ossifying Fibroma ◽  
Rare Group

Juvenile ossifying fibromas (JOFs) are a rare group of fibro-osseous lesions, typically of odontogenic origin. Juvenile psammomatoid ossifying fibroma (JPOF) is one variant, that is, histopathologically distinguished by spherical ossicles resembling psammoma bodies. JPOF tumours are most commonly found in craniofacial skeletal structures and can be locally aggressive. Thus, early management by complete surgical excision is crucial for good outcomes, although recurrence is still possible. Secondary aneurysmal bone cyst (ABC) formation has been reported with JOF lesions, but less commonly with the JPOF variant. We describe an unusual case of JPOF that presented in the calcaneus with secondary ABC formation.

Aneurysmal bone cyst of the cuboid

1990 ◽  
Vol 80 (11) ◽  
pp. 588-594 ◽  
Author(s):  
KB Kashuk ◽  
JR Hanft ◽  
JA Schabler ◽  
KE Kado ◽  
BD Wolosky
Keyword(s):  
Literature Review ◽  
Ankle Joint ◽  
Aneurysmal Bone Cyst ◽  
Unusual Case ◽  
Bone Cyst ◽  
Bone Cysts ◽  
Rare Entity ◽  
Documented Case ◽  
Aneurysmal Bone Cysts

Aneurysmal bone cysts are a rare entity encountered in podiatric medicine. The frequency of aneurysmal bone cysts distal to the ankle joint is low. The authors present a literature review of the etiologies and possible treatments of an aneurysmal bone cyst. An unusual case of an aneurysmal bone cyst in the cuboid is also presented. Only one other documented case of an aneurysmal bone cyst in the cuboid has been reported since 1967.

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