TY - JOUR
T1 - Intraosseous myofibroma of the mandible
T2 - A case report and review of the literature
AU - Cannon, Scott
AU - Hammad, Yousef
AU - Schlieve, Thomas
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/12
Y1 - 2021/12
N2 - Soft tissue myofibromas of the head and neck are relatively common lesions diagnosed within the first two decades of life; however, these myofibromas are rarely found to affect the jaw bones. Myofibromas that do develop within the bone are referred to as intraosseous myofibromas (IM). A thorough search and review of the literature has found only five cases of IM impacting the mandible of an adult patient. The current case report describes a myofibroma impacting the right posterior mandible in a 44-year-old male patient with no previous history of pathology or surgery within the affected area. Histologic examination of the incisional biopsy specimen revealed a proliferation of spindle cells, and the spindle cells showed positivity for SMA on immunohistochemical staining supporting the diagnosis of myofibroma. The final pathology results of the subsequent composite resection of the lesion yielded a 1.5cm myofibroma that was < 1mm from the nearest bone/soft tissue edge; the resection margin was uninvolved by tumor. The purpose of this case report is to present the sixth case of IM of the mandible of an adult patient and to review the pertinent radiographic and clinical features, and necessary methods for diagnosis and treatment of this rare entity.
AB - Soft tissue myofibromas of the head and neck are relatively common lesions diagnosed within the first two decades of life; however, these myofibromas are rarely found to affect the jaw bones. Myofibromas that do develop within the bone are referred to as intraosseous myofibromas (IM). A thorough search and review of the literature has found only five cases of IM impacting the mandible of an adult patient. The current case report describes a myofibroma impacting the right posterior mandible in a 44-year-old male patient with no previous history of pathology or surgery within the affected area. Histologic examination of the incisional biopsy specimen revealed a proliferation of spindle cells, and the spindle cells showed positivity for SMA on immunohistochemical staining supporting the diagnosis of myofibroma. The final pathology results of the subsequent composite resection of the lesion yielded a 1.5cm myofibroma that was < 1mm from the nearest bone/soft tissue edge; the resection margin was uninvolved by tumor. The purpose of this case report is to present the sixth case of IM of the mandible of an adult patient and to review the pertinent radiographic and clinical features, and necessary methods for diagnosis and treatment of this rare entity.
KW - Intraosseous myofibroma
KW - Myofibroma
KW - Oral and maxillofacial pathology
KW - Oral and maxillofacial surgery
UR - http://www.scopus.com/inward/record.url?scp=85122757153&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122757153&partnerID=8YFLogxK
U2 - 10.1016/j.omsc.2021.100234
DO - 10.1016/j.omsc.2021.100234
M3 - Article
AN - SCOPUS:85122757153
SN - 2214-5419
VL - 7
JO - Oral and Maxillofacial Surgery Cases
JF - Oral and Maxillofacial Surgery Cases
IS - 4
M1 - 100234
ER -