Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report

المؤلفون المشاركون

Allen, Chad N.
Nguyen, Katina
Tandon, Rahul
Stringer, Dale E.

المصدر

Case Reports in Surgery

العدد

المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2014-09-01

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

Inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion found in the maxillofacial region.

Its frequency diminishes further when found in the bone.

Although classification has varied throughout its history, the histologic features are often diagnostic, particularly with its strong association with anaplastic lymphoma kinase-1 (ALK-1) staining.

The current mode of treatment for such a lesion is surgical removal with careful followup.

In this rare case report, we describe the diagnosis and treatment in a 16-year-old male.

Although this rare pathology can present as—and at times mimic—more serious pathologies, it is important for the attending surgeon to initially manage the pathology conservatively.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Stringer, Dale E.& Allen, Chad N.& Nguyen, Katina& Tandon, Rahul. 2014. Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report. Case Reports in Surgery،Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-1034983

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Stringer, Dale E.…[et al.]. Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report. Case Reports in Surgery No. 2014 (2014), pp.1-4.
https://search.emarefa.net/detail/BIM-1034983

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Stringer, Dale E.& Allen, Chad N.& Nguyen, Katina& Tandon, Rahul. Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report. Case Reports in Surgery. 2014. Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-1034983

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1034983