हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।
ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं
Mohammad Hosein Kalantar Motamedi, Ali Ebrahimi, Ahmad Behroozian, Neda Kargahi, Hamid Reza Rasouli and Ali Shams Nouraie
Purpose: This study aimed to assess the prevalence, demographics, clinicohistopathological features and treatment outcomes of maxillofacial aneurysmal bone cysts (ABCs) in Isfahan.
Materials and method: A unicenter retrospective study of patient charts dated from 1987-2013 (26 years) was undertaken to assess maxillofacial ABCs. Variables such as age, gender, location (maxilla, mandible, anterior or posterior segments), histological type (solid, mixed, vascular), signs, symptoms, radiographic features ,treatment modalities and outcomes of this lesion were evaluated by the authors. The data was analyzed using SPSS 20 software (p<0.05).
Result: 16 patients were diagnosed and treated in our study, which included 6 (37.5%) males and 10 (62.5%) females. There was a significant female predilection (p<0.05). The mean age of occurrence was16.2 ± 7.9 years ranging from 6 to 28 years.The prevalence was not significantly higher in any decade of life. The rate of affliction was 0.6 case per year. ABC was significantly more common in the mandible (p<0.05) and the posterior areas (p<0.05). The most common histopathological type was the mixed type (p<0.05).Bony hard Swelling was the most common clinical finding (p<0.05) and all cases were radiolucent. All cases were treated with excision and curettage. Two patients (12.5%) showed recurrence during the follow-up period (1-26 years).There was no relationship between recurrence and other parameters.
Conclusion: ABCs of the jaws are rare lesions with variable presentation and often respond well to excision and curettage. Apparently it seems that there is no need to do more aggressive surgery because recurrence is low.