scholarly journals Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report

ENT Updates ◽  
2017 ◽  
Vol 7 (3) ◽  
pp. 157-160
Author(s):  
Özlem Ünsal ◽  
Pınar Soytaş ◽  
Fevziye Kabukçuoğlu ◽  
Berna Uslu Coşkun
Keyword(s):  
Case Report ◽  
Skull Base ◽  
Rare Case ◽  
Ossifying Fibroma ◽  
Orbital Wall ◽  
Rare Case Report ◽  
Psammomatoid Ossifying Fibroma ◽  
Wall Invasion

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 Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report

2014 ◽  
Vol 7 (1) ◽  
pp. 28-30
Author(s):  
Varsha Varshney ◽  
Gaurav Gupta ◽  
Mohnish Grover ◽  
Vikas Devra
Keyword(s):  
Case Report ◽  
Skull Base ◽  
Rare Case ◽  
Malignant Neoplasm ◽  
Complete Recovery ◽  
Burkitt’S Lymphoma ◽  
Anterior Skull Base ◽  
Burkitt's Lymphoma ◽  
Loss Of Vision ◽  
Rare Case Report

ABSTRACT Burkitt's lymphoma is a malignant neoplasm rarely found in paranasal sinuses and skull base. We report a rare case of Burkitt's lymphoma of anterior skull base associated with acute loss of vision. A 10 years old boy presented with history of headache, diminution of vision in right eye since 15 days. Biopsy showed diffuse NHL of Burkitt's type. After treatment with chemotherapy there was complete recovery in vision. How to cite this article Gupta G, Devra V, Grover M, Varshney V. Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report. Clin Rhinol An Int J 2014;7(1):28-30.

Peripheral Cemento Ossifying Fibroma- A Rare Case Report

2014 ◽  
Vol 1 (3) ◽  
pp. 55-58
Author(s):  
Jaai Rane ◽  
Jasmin Winnier J ◽  
Rupinder Bhatia
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ossifying Fibroma ◽  
Rare Case Report

scholarly journals Peripheral cemento-ossifying fibroma – A rare case report

2022 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Noopur Kaushik ◽  
Nikhil Srivastava ◽  
Vivek Rana ◽  
Chirag Suhane
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ossifying Fibroma ◽  
Rare Case Report

scholarly journals Conglomeration of Trabecular and Psammomatoid variants of juvenile ossifying fibroma - a rare case report

2017 ◽  
Vol 5 (6) ◽  
pp. 816-821 ◽  
Author(s):  
Lipsa Bhuyan ◽  
Abikshyeet Panda ◽  
Kailash Chandra Dash ◽  
Mohiddin S. Gouse ◽  
Kiran Misra
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ossifying Fibroma ◽  
Juvenile Ossifying Fibroma ◽  
Rare Case Report

scholarly journals Ossifying Fibroma of Dorsal Spine in a Postpartum Female: A Rare Case Report

2019 ◽  
Vol 08 (02) ◽  
pp. 136-138
Author(s):  
Musali Siddartha Reddy ◽  
Gollapudi Prakash Rao ◽  
Mohammed Imran ◽  
Uday Goutam Nookathota
Keyword(s):  
Case Report ◽  
Postpartum Period ◽  
Rare Case ◽  
Lower Limbs ◽  
Dorsal Spine ◽  
Postpartum Woman ◽  
Ossifying Fibroma ◽  
Diagnostic Dilemma ◽  
Spinal Stabilization ◽  
Rare Case Report

AbstractA rare case of monostotic ossifying fibroma of the dorsal spine in a postpartum woman is being described. Ossifying fibromas of the spine are very rare tumors. They are components of benign fibro-osseous lesions. We report a case of an 18-year-old woman, who presented with complaints of weakness of both the lower limbs in the immediate postpartum period and was diagnosed with ossifying fibroma of the dorsal [D3] vertebral body. The tumor was excised followed by spinal stabilization. Histopathologic findings were consistent with ossifying fibroma. Postoperative period was uneventful. Monostotic variant of ossifying fibroma in the dorsal spine is an extremely rare tumor, and its presence in the postpartum period adds on to the diagnostic dilemma. Hence this case report can be kept in mind while evaluating a case presenting with complaints of weakness of both the lower limbs in the immediate postpartum period.

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