Multiple peripheral odontogenic fibroma, world health organization type, and central giant cell granuloma: A case report of an unusual association

1993 ◽  
Vol 51 (3) ◽  
pp. 325-328 ◽  
Author(s):  
Giuseppe Ficarra ◽  
J. Philip Sapp ◽  
Lewis R. Eversole
2019 ◽  
Vol 2 (1) ◽  
pp. 01-04
Author(s):  
Nilotpol Kashyap ◽  
Manisha Upadhyay ◽  
Rupam Tripathi ◽  
Pallavi Pawar ◽  
Ranjeet Kumar Prasad Sah ◽  
...  

Central giant cell granuloma (central giant cell granuloma) is an uncommon benign bony lesion that occurs in the mandible and maxilla and accounts for approximately 7% of all benign tumours of the jaws [1]. The World Health Organization (WHO) has defined central giant cell granuloma as an intraosseous lesion consisting of cellular fibrous tissue that contains multiple foci of haemorrhage, aggregations of multinucleated giant cells and occasional trabeculae of woven bone [2]. Central giant cell granuloma occurs predominantly in children or young adults, with approximately 75%of cases presenting before 30 years of age although presentation can occur at any age [3]. Females are affected more frequently than males, with a ratio of 2:1


2017 ◽  
Vol 1 (1) ◽  
pp. s-0037-1601482
Author(s):  
Pietro Boni ◽  
Alberto Bozzetti ◽  
Valeria Morganti ◽  
Giorgio Novelli ◽  
Davide Sozzi

Central giant cell granuloma (CGCG) is a relatively rare intraosseous lesion, described by the World Health Organization as a localized proliferation consisting of fibrous tissue with hemorrhage deposits, the presence of osteoclast-like cells, and reactive bone formation. In this article, the authors present their experience in managing a wide, aggressive CGCG of the whole tooth-bearing mandible in a 9-year-old pediatric patient. The extension of the lesion and the age of the patient have presented a double challenge concerning treatment and outcome. If fact the main objective remains a correct therapeutic treatment, focused on healing the patient and avoiding recurrences, the clinician must be careful in preventing an excessive morbidity. The authors decided to treat the young patient with intralesional corticosteroid therapy, reserving surgery in case of non-response or for subsequent refinements. In this article is presented the authors’ conservative treatment protocol with intralesional corticosteroid injection and their results are compared with literature's data.


1970 ◽  
Vol 1 (1) ◽  
pp. 56-58
Author(s):  
SC Kohli ◽  
UK Shrestha ◽  
VM Alurkar ◽  
A Maskey ◽  
M Parajuli ◽  
...  

The global program to eliminate Lymphatic Filariasis created by The World Health organization in 1997 is based on mass administration of single annual doses of diethylcarbamazine ( DEC) plus albendazole in non African regions and of albendazole plus ivermectin in Africa. The usual side effects of DEC treatment include fever, chills, arthralgia, headaches, nausea, and vomiting. Albendazole is associated with relatively few side effects consisting of occasional nausea, vomiting, abdominal pain, headache, reversible alopecia, elevated aminotransferases and rarely leucopenia and rash. We report a case of polyneuropathy in a young individual following DEC and albendazole during mass drug administration. Keywords: Albendazole; DEC; Polyneuropathy. DOI: http://dx.doi.org/10.3126/njms.v1i1.5800   Nepal Journal of Medical Sciences. 2012; 1(1): 56-58


2016 ◽  
Vol 10 (3) ◽  
pp. 393-397
Author(s):  
Soukayna Bahbah ◽  
Saloua Dghoughi ◽  
Hakima Chhoul ◽  
Wafaa El Wady

2021 ◽  
Vol 12 (6) ◽  
pp. 1-4
Author(s):  
Tejavathi Nagaraj ◽  
Ijum Doye ◽  
Durga Okade ◽  
Soniya Kongbrailatpam

2021 ◽  
Author(s):  
Katrien Brijs ◽  
Koenraad Veys ◽  
Serge Schepers ◽  
Heidi Segers ◽  
Constantinus Politis

2015 ◽  
Vol 5 (1) ◽  
pp. 11
Author(s):  
Garima Singh ◽  
Ashish Thakur ◽  
Heena Sadiq ◽  
Priti Gupta

Author(s):  
SAMARA ANDREOLLA LAZARO ◽  
HENRIQUE CESCA ◽  
TIAGO NASCIMENTO MILETO ◽  
FRANKLIN DAVID GORDILLO YEPEZ ◽  
CASSIAN TAPARELLO ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document