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

Joint Authors

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

Source

Case Reports in Surgery

Issue

Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-4, 4 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2014-09-01

Country of Publication

Egypt

No. of Pages

4

Main Subjects

Medicine

Abstract 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.

American Psychological Association (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

Modern Language Association (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

American Medical Association (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

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1034983