scholarly journals Juvenile ossifying fibroma: case report and literature review. Management and differential diagnosis

2018 ◽  
Vol 24 (2) ◽  
pp. 67-71
Author(s):  
Sarah Lemoine ◽  
Elisabeth Cassagnau ◽  
Hélios Bertin ◽  
Maria Poisson ◽  
Pierre Corre ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rapid Growth ◽  
Benign Tumor ◽  
Early Stage ◽  
Bone Matrix ◽  
Fibrous Tissue ◽  
Ossifying Fibroma ◽  
Juvenile Ossifying Fibroma ◽  
Review Management

Introduction: Juvenile ossifying fibroma (JOF) is a rare neoplasm characterized by the replacement of the normal bone matrix with osteo-fibrous tissue. It has the tendency to be locally aggressive despite its benign character and to have a strong tendency for recurrence. Observation: In this case report, the patient is a young man, aged 16, with rapidly advancing maxillary swelling. We describe the diagnostic procedure, the surgical procedure and the differential diagnosis to be eliminated. Discussion: The clinical presentation of JOF, and its rapid growth, can cause fear of other pathologies such as osteosarcoma. The radiological characteristics should reassure the practitioner and a histological examination confirmed the diagnosis. Conclusion: JOF is a benign tumor. It should be operated on at an early stage because of its rapid growth. In its clinical and histological presentation, its trabecular form may mimic an osteosarcoma.

JUVENILE OSSIFYING FIBROMA AND FIBROUS DYSPLASIA: A CASE REPORT OF A COMPLEX DIFFERENTIAL DIAGNOSIS

2020 ◽  
Vol 129 (1) ◽  
pp. e127
Author(s):  
MALENA REGINA DE FREITAS E. SILVA ◽  
FRANCISCO ARTUR FORTE OLIVEIRA ◽  
PAULO GOBERLÂNIO DE BARROS SILVA ◽  
TÁCIO PINHEIRO BEZERRA ◽  
JOÃO PAULO VELOSO PERDIGÃO ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Fibrous Dysplasia ◽  
Ossifying Fibroma ◽  
Juvenile Ossifying Fibroma

scholarly journals Atypical keratoacanthoma: a case report

2020 ◽  
Vol 23 (6) ◽  
pp. 364-372
Author(s):  
Elena S. Snarskaya ◽  
L. M. Shnakhova ◽  
D. A. Gomich ◽  
K. D. Vasileva
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Skin Cancer ◽  
Squamous Cell ◽  
Rapid Growth ◽  
Spontaneous Regression ◽  
Clinical Case ◽  
Treatment Approach ◽  
Early Stage ◽  
Immunohistochemical Methods

In this article we summarized etiopathogenesis and clinical data, presented classification and described diagnosis challenges. One of the most common epithelial tumors, keratoacanthoma (KA) is characterized by rapid growth, histopathological features of squamous cell skin cancer and spontaneous regression tendency. Differential diagnosis of typical and atypical KA can be challenging since an early stage atypical KA may present similar to typical KA. Immunomorphological and immunohistochemical methods are particularly relevant for detecting atypical KA, making it possible to reliably differentiate it from squamous cell skin cancer. Years of experience in the management of KA patients, as well as foreign researchers data, suggest that the treatment approach should be based on the differentiation of clinical features of a typical KA from an atypical one.This report describes a clinical case of a giant keratoacanthoma.

scholarly journals Laparoscopic Resection of a Giant Dedifferentiated Primary Retroperitoneal Mucinous Cystadenoma (PRMC) in a Young Woman: A Case Report and Literature Review

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Wu L ◽  
Li X ◽  
Li J ◽  
Lai Y
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Benign Tumor ◽  
Laparoscopic Resection ◽  
Abdominal Cavity ◽  
Mucinous Cystadenoma ◽  
Rare Benign Tumor ◽  
Primary Retroperitoneal

Background: PRMC is a very rare benign tumor of the abdominal cavity that usually occurs in women, and PRMC demonstrate no specific findings on CT. There are many reports on the differential diagnosis and discussion of PRMC imaging, but there are few reports on the treatment of dedifferentiated PRMC using laparoscopic resection and postoperative follow-up.

scholarly journals Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report

2016 ◽  
Vol 6 (1) ◽  
pp. 45-51
Author(s):  
Deepa Das Achath ◽  
Abhishek Sanjay Ghule ◽  
Preeti Kanchan-Talreja ◽  
Sunanda Bhatnagar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histological Analysis ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Appropriate Treatment ◽  
Juvenile Ossifying Fibroma ◽  
Rare Case Report

ABSTRACT Fibroosseous lesions of the jaws, including juvenile ossifying fibroma (JOF), pose diagnostic and therapeutic difficulties due to their clinical, radiological, and histological variability. There are two histological varieties of it, one as psammomatoid type and second as trebacular type; here, we present a trebacular type, which is a rare variety. After the clinical examination, radiological and histological analysis, it was diagnosed as juvenile trebacular ossifying fibroma. Although JOF is an uncommon clinical entity, its aggressive local behavior and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment, and, especially, follow-up the patient over the long term. How to cite this article Ghule AS, Achath DD, Kanchan- Talreja P, Bhatnagar S. Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report. J Contemp Dent 2016;6(1):45-51.

scholarly journals Juvenile Ossifying Fibroma of the Maxilla: A Case Report

1970 ◽  
Vol 9 (1) ◽  
pp. 49-52
Author(s):  
NTH Syarifah ◽  
AR Roselinda ◽  
M Irfan
Keyword(s):  
Case Report ◽  
Clinical Presentation ◽  
Age Of Onset ◽  
Medical Science ◽  
Ossifying Fibroma ◽  
Local Growth ◽  
Juvenile Ossifying Fibroma

Juvenile ossifying fibroma (JOF) is an uncommon, benign, bone-forming neoplasm with aggressive local growth that is distinguished from other fibro-osseous lesions primarily by its age of onset, clinical presentation and potential behaviour. We reported a 10 year old girl presenting with a growth in the left upper buccal gingiva which later was diagnosed as juvenile ossifying fibroma. The nature of the disease and outline of management were discussed. Keywords: Ossifying fibroma; Juvenile; Maxilla. DOI: 10.3329/bjms.v9i1.5231 Bangladesh Journal of Medical Science Vol.09 No.1 Jan 2010 49-52

scholarly journals Psammomatoid Juvenile Ossifying Fibroma: A Case Report with Literature Review

2010 ◽  
Vol 22 ◽  
pp. S53-S57
Author(s):  
Preeti Nair ◽  
Anil Kumar ◽  
Karthik Hegde ◽  
Shiba Neelakantan
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Ossifying Fibroma ◽  
Juvenile Ossifying Fibroma

scholarly journals Juvenile Psammomatoid Ossifying Fibroma of Fronto-Ethmoid Complex Mimicking Fibrous Dysplasia: Case Report

2018 ◽  
Vol 8 (1) ◽  
pp. 33-36
Author(s):  
Kapil Adhikari ◽  
Ashok Raj Pant ◽  
Sapana Koirala
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Fibrous Dysplasia ◽  
Histopathological Examination ◽  
Plain Radiograph ◽  
Ossifying Fibroma ◽  
Histopathological Findings ◽  
Psammomatoid Ossifying Fibroma

Juvenile Psammomatoid Ossifying Fibromais a rare fibro-osseous tumor seen in children and adolescentand mostly arising from the cranio-facial bone.We report a case of 18-year-old boy who presented with diplopiaand progressive right fronto-orbital swelling. On plain radiograph and CT, it was diagnosed as fibrous dysplasiaand mucocele as differential diagnosis. The tumor was resected and histopathological examination showed psammomatoid features. Therefore, the diagnosis of Juvenile Psammomatoid Ossifying Fibroma must be based on both radiological and histopathological findings.

JUVENILE OSSIFYING FIBROMA: A CASE REPORT WITH DIAGNOSTIC CHALLENGE

2020 ◽  
Vol 129 (1) ◽  
pp. e123-e124
Author(s):  
ANANDA AMARAL SANTOS ◽  
FERNANDA PAULA YAMAMOTO-SILVA ◽  
WILSON JOSÉ MARIANO ◽  
MARCONDES SENA FILHO ◽  
LEONARDO AMARAL DOS REIS ◽  
...  
Keyword(s):  
Case Report ◽  
Ossifying Fibroma ◽  
Diagnostic Challenge ◽  
Juvenile Ossifying Fibroma
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