scholarly journals Rare case of a recurrent juvenile ossifying fibroma of the lumbosacral spine

2018 ◽  
Vol 28 (6) ◽  
pp. 647-653 ◽  
Author(s):  
Cecilia L. Dalle Ore ◽  
Darryl Lau ◽  
Jessica L. Davis ◽  
Michael M. Safaee ◽  
Christopher P. Ames

Juvenile ossifying fibroma (JOF) is a rare benign bone tumor that occurs most frequently in the craniofacial bones of children and young adults. There are few case reports that describe its involvement outside the craniofacial skeleton, especially within the spinal column. While JOF is classified as a benign lesion, it may be locally aggressive and demonstrate a high propensity for recurrence, even after resection. Definitive surgical management may be challenging in naive cases, but it is particularly challenging in recurrent cases and when extensive spinal reconstruction is warranted. In this report, the authors describe the diagnosis and surgical management of a 29-year-old man who presented with a large recurrent sacral trabecular-subtype JOF. A review of literature regarding JOFs, management of recurrent primary spinal tumors, and sacral reconstruction are discussed.

2020 ◽  
Vol 130 (3) ◽  
pp. e172-e173
Author(s):  
LUAN ÉVERTON GALDINO BARNABÉ ◽  
LEONARDO COSTA DE ALMEIDA PAIVA ◽  
ANÍBAL HENRIQUE BARBOSA LUNA ◽  
DAVI FELIPE NEVES COSTA ◽  
DANIELA PITA DE MELO ◽  
...  

2009 ◽  
Vol 19 (2) ◽  
pp. 116 ◽  
Author(s):  
Simi Thankappan ◽  
Sherin Nair ◽  
Valsa Thomas ◽  
KP Sharafudeen

Author(s):  
Pedro Clarós ◽  
Sofia Polainas ◽  
Marta Fortuny ◽  
Andres Clarós

<p class="abstract">Osseous tumors in the craniofacial skeleton of young patients are not very frequent, and tumors involving the walls of the orbital cavity are even more infrequent. Despite being usually slow-growing, even small neoformations can have a local aggressive behavior, displacing and compressing vital structures, and so it is important to perform an early diagnosis in order to avoid the tumor to pose problems on the optic nerve and threaten vision. The case that we are presenting shows an ossifying fibroma in a 19-year-old male from Ethiopia, a benign lesion whose progressive growth caused proptosis and downward displacement of the left eye. Following an adequate radiological diagnosis, we were able to delimit the fibroma existence and location. The surgery was conducted in a conservative form, allowing the patient not to suffer from post-surgery malformations. Histopathological diagnosis was compatible with juvenile ossifying fibroma, psammomatoid variant, arising from an uncommon location – the roof of the orbit.  </p>


2021 ◽  
Vol 14 (3) ◽  
pp. e240952
Author(s):  
Santhosh Rao ◽  
Vandita Singh ◽  
Abdul Hafeez A ◽  
Subham S Agarwal

Psammomatoid Juvenile ossifying fibroma (PsJOF) is a rare benign fibro-osseous lesion characterised to grow to unusually large size very rapidly. Its usual presentation is in younger age group mostly children and predominately involving the Sino-Naso-Orbital region. Its aggressive nature gimmicks a malignant lesion but it is rather a benign lesion with a higher recurrence rate than the conventional ossifying fibroma but lacking metastatic potential. The high recurrence rate makes it essential that the lesion is not reconstructed immediately and thorough monitoring in the follow-up period. Lesion of such clinical importance needs to be diagnosed preoperatively to provide a better and radical surgical treatment option, but the variability in its presentation as seen in this case makes it even harder to diagnose. We aim to draw attention to the rare phenomena that PsJOF presents to help readers broaden their purview in diagnosis and thereby manage them accordingly.


2012 ◽  
Vol 73 (S 02) ◽  
Author(s):  
K. Tekeli ◽  
A. Toma ◽  
P. Minhas ◽  
M. Manisali

2006 ◽  
Vol 9 (4) ◽  
pp. E668-E674 ◽  
Author(s):  
Omer Dogan ◽  
Metin Demircin ◽  
Suheyla Ozkutlu ◽  
Ilhan Pasaoglu

2016 ◽  
Vol 45 (3) ◽  
pp. 368-376 ◽  
Author(s):  
J. Han ◽  
L. Hu ◽  
C. Zhang ◽  
X. Yang ◽  
Z. Tian ◽  
...  

2018 ◽  
Vol 79 (05) ◽  
pp. 408-415 ◽  
Author(s):  
Jan Victor ◽  
Thibault Poujade ◽  
Nadine Hollevoet ◽  
Gregoire Chick

Aims To identify the frequency of reports of sporadic schwannomatosis, the types of patients affected, and the nerves affected. Patients and Methods We identified all case reports and case series that reported on patients with sporadic schwannomatosis according to established criteria. Results The initial search yielded 1,597 studies, of which 15 were included. A total of 38 of 55 individuals met the inclusion criteria. The mean age of the patients was 48 years; 41% were male. Thirty-three patients had peripheral nerve tumors, and 17 had spinal tumors. Twelve had tumors in both locations. Tumor distribution was unilateral in 25 of 30 cases (83.3%) and segmental (limited to one limb or five or fewer contiguous segments of the spine) in 28 of 38 cases (73.7%). Conclusion This systematic review quantified the number of individuals who meet the criteria for sporadic schwannomatosis and better described this population to facilitate the classification of neurofibromatosis in regard to the 2005 consensus statement. Unilateral or segmental distribution of nerve tumors are key aspects when dealing with multiple noncutaneous schwannomas without involvement of the vestibular nerve.


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