Juvenile psammomatoid ossifying fibroma in paranasal sinus and skull base

2017 ◽  
Vol 137 (7) ◽  
pp. 743-749 ◽  
Author(s):  
Mingjie Wang ◽  
Bing Zhou ◽  
Shunjiu Cui ◽  
Yunchuan Li
2019 ◽  
Vol 125 ◽  
pp. e843-e848 ◽  
Author(s):  
Ke Wang ◽  
Xiu-Jian Ma ◽  
Shu-Yu Hao ◽  
Jiang Du ◽  
Li-Wei Zhang ◽  
...  

2018 ◽  
Vol 29 (5) ◽  
pp. e497-e499 ◽  
Author(s):  
Do-Youn Kim ◽  
Oh Hyeong Lee ◽  
Gyeong Cheol Choi ◽  
Jin Hee Cho

ENT Updates ◽  
2017 ◽  
Vol 7 (3) ◽  
pp. 157-160
Author(s):  
Özlem Ünsal ◽  
Pınar Soytaş ◽  
Fevziye Kabukçuoğlu ◽  
Berna Uslu Coşkun

2016 ◽  
Vol 17 (3) ◽  
pp. 318-323 ◽  
Author(s):  
Cristina Barrena López ◽  
Alicia Bollar Zabala ◽  
Enrique Úrculo Bareño

Juvenile psammomatoid ossifying fibroma (JPOF) is a fibroosseous tumor that arises in the craniofacial bones in young people. This lesion usually originates in the jaw, orbit, and ethmoid complex but can also be associated with the skull base and calvaria. Diagnosis must be made based on observing typical radiological and histopathological features. Although JPOF is a rare pathological entity, neurosurgeons must consider this odontogenic lesion in the differential diagnosis of skull masses given the lesion’s aggressive behavior and locally invasive growth. Treatment must be gross-total resection. In the following article, the authors present a case of cranial JPOF and discuss various aspects of this entity.


2013 ◽  
Vol 11 (6) ◽  
pp. 687-691 ◽  
Author(s):  
Nathan C. Rowland ◽  
Walter J. Jermakowicz ◽  
Tarik Tihan ◽  
Ivan H. El-Sayed ◽  
Michael W. McDermott

Juvenile psammomatoid ossifying fibroma (JPOF) is a benign fibro-osseous lesion typically associated with the jaw, paranasal region, or orbit. However, JPOF may also originate from the skull base and locally invade the cranium. In published reports, intracranial JPOFs constitute only a small percentage of cases, and therefore it is not known whether more aggressive behavior typifies this distinct population of JPOFs compared with those in other locations. Nevertheless, JPOF histopathology is characterized by a number of active processes, including cystic transformation, that may precipitate violation of skull base boundaries. In the following article, the authors present a case of skull base JPOF that underwent cystic expansion in a young girl, produced a focal neurological deficit, and was resolved using a staged surgical approach.


2020 ◽  
Author(s):  
Cheyanne M. Silver ◽  
Lucas P. Carlstrom ◽  
Christopher S. Graffeo ◽  
Avital Perry ◽  
Garret W. Choby ◽  
...  

2012 ◽  
Vol 55 (3) ◽  
pp. 146-149
Author(s):  
Ibrahim Erdim ◽  
Zahide Mine Yazici ◽  
Rasim Yilmazer ◽  
Nurten Sever ◽  
Fatma Tulin Kayhan

Cemento-ossifying fibroma is a well-bordered, slow-growing, benign fibro-osseous disease. Although its localization is generally in the mandible, it can be seen in any area of the craniofacial region. Radiology and histopathology help to diagnose the condition. Treatment is based on close observation and/or surgical excision. In this case, we report the case of a 62-year-old male patient who had a large radiological appearance, cemento-ossifying fibroma in the paranasal sinuses.


2019 ◽  
Author(s):  
Junxiao Gao ◽  
Zhenchao Zhu ◽  
Yudong Ye ◽  
Qianhui Qiu ◽  
Ming Fu

Abstract Background Chondrosarcoma(ChSa) is a rare malignant tumor. But it’s necessary to discuss the clinical characteristics and treatments for ChSa of paranasal sinus and the skull base. Methods The clinical characteristics of ChSa of paranasal sinus and skull base in 10 patients (6 males and 4 females) from 2001 to 2017 were analyzed. They all underwent by endoscopic surgery . The patients’ age ranged from 18 to 47 years, with a median of 35 years. Clinical symptoms: stuffy, nose bleeding, runny, headache, diplopia, eye outreach limited, blurred vision and even blindness. Surgery methods:under nasal endoscopy, after the attachment sites of the tumors to normal tissues were confirmed, the tumors were peeled off along the clear boundary between the tumors and normal tissues, and the potential residual tumor tissues on bones were cleared by a drill. Results All patients were treated with endoscopic surgery,followed up postoperatively for 24 to 108 months, with a median of 36 months. 8 of 10 patients were no recurrence,2 were alive with tumor. Conclusion ChSa of paranasal sinus and skull base can be treated by nasal endoscopic surgery with good clinical results.


2021 ◽  
pp. 1-3
Author(s):  
Sudhagar Eswaran ◽  
Namrataa S ◽  
Prasanna Kumar S

BACKGROUND: Mucocele is a true cystic expansile mass filled with mucus resulting from obstruction of the sinus ostia. Prompt diagnosis and management are needed to avoid complications due to the intracranial or intra-orbital extension. OBJECTIVES: To audit data of mucocele of the paranasal sinuses in a tertiary center, to review the literature regarding the clinical features and the management of mucocele in the paranasal sinus and to emphasize the iatrogenic causes of mucocele after the development of Endoscopic Skull Base Surgeries. MATERIALS AND METHODS: A retrospective analysis of etiology, clinical presentation, sinuses involved, operative technique, complication, recurrence were interpreted. RESULTS: The mean age of 16 patients managed is 49. Location:37% frontal,19% ethmoidal,19% frontoethmoidal,19% sphenoidal,6% maxillary. The iatrogenic cause was 44%. Symptoms included proptosis, external swelling, nasal block, and discharge, and vision loss. Complications were orbital abscess and skull base defect. 14 patients underwent endoscopic procedures-excision or marsupialization. One patient underwent craniotomy; one patient combined approach was performed. One patient had a recurrence. CONCLUSION: Mucocele of the paranasal sinuses is still a rare clinical scenario and it is imperative to note that any delay in diagnosis and management can lead to expansion and erosion of the bony wall of the sinuses and causing complications.


2020 ◽  
Vol 59 (1) ◽  
pp. 6-12
Author(s):  
Hiroyuki Morishita ◽  
Masayoshi Kobayashi ◽  
Kazuhiko Takeuchi

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