Postauricular Myofibroma of the Facial Canal: A Case Report
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Myofibromatosis is a proliferative disorder characterized by the development of soft tissue neoplasms referred to as myofibromas that predominantly occur in infants and young children. These lesions have been described using varied terminologies since they were first reported in 1951. However, these neoplasms are histopathologically characterized by benign fibroblast and myofibroblast proliferation containing a biphasic presentation of spindle-shaped cells surrounding a central zone of less differentiated cells arranged in a hemangiopericytoma-like pattern in all cases. Usually, myofibromatosis occurs in children aged <2 years and is observed at birth in nearly 60% of cases. We report a rare case of myofibroma in an 8-year-old boy who presented with an approximately 6-month history of a left postauricular mass. Histopathological evaluation of the resected mass confirmed the diagnosis
Abstract
Myofibromatosis is a proliferative disorder characterized by the development of soft tissue neoplasms referred to as myofibromas that predominantly occur in infants and young children. These lesions have been described using varied terminologies since they were first reported in 1951. However, these neoplasms are histopathologically characterized by benign fibroblast and myofibroblast proliferation containing a biphasic presentation of spindle-shaped cells surrounding a central zone of less differentiated cells arranged in a hemangiopericytoma-like pattern in all cases. Usually, myofibromatosis occurs in children aged <2 years and is observed at birth in nearly 60% of cases. We report a rare case of myofibroma in an 8-year-old boy who presented with an approximately 6-month history of a left postauricular mass. Histopathological evaluation of the resected mass confirmed the diagnosis
참고문헌 (15)
- Venkatesh V, "Myofibroma-a rare entity with unique clinical presentation", J Maxillofac Oral Surg, 14(Suppl 1), pp.64~68 (2015)
- Dhupar A, "Solitary intraosseous myofibroma of the jaw : a case report and review of literature", Children(Basel), 4, pp.91~ (2017)
- Wisecarver IR, "Posterior auricular mass", Eplasty, 17, pp.ic16~ (2017)
- Lewis JS Jr, "Spindle cell lesions--neoplastic or non-neoplastic? : spindle cell carcinoma and other atypical spindle cell lesions of the head and neck", Head Neck Pathol, 2, pp.103~110 (2008)
- Asthana A, "Unusual presentation of a rare soft tissue neoplasm;myofibroma of the ear", Int J Sci Res, 3, pp.1051~1053 (2014)
- Chung EB, "Infantile myofibromatosis", Cancer, 48, pp.1807~1818 (1981)
- Yi KM, "Myofibroma", myofibromatosis : MDCT and MR imaging findings in 24 patients with radiological-pathological correlation, 2020, pp.20, 100~
- Narayen V, "Myofibroma of the gingiva : a rare case report and literature review", Case Rep Dent, 2015, pp.243894~ (2015)
- Brasileiro BF, "Myofibroma of the oral cavity. A rare spindle cell neoplasm", Med Oral Patol Oral Cir Bucal, 15, pp.e596~e600 (2010)
- Tanaka Y, "Solitary myofibroma of the mandible in an adult with magnetic resonance imaging and positron emission tomography findings : a case report", World J Surg Oncol, 12, pp.69~ (2014)
- Beck JC, "Pediatric myofibromatosis of the head and neck", Arch Otolaryngol Head Neck Surg, 125, pp.39~44 (1999)
- Li T, "Parotidectomy by an endoscopic-assisted postauricular-groove approach", Head Neck, 41, pp.2851~2859 (2019)
- Chu JK, "Postoperative facial palsy after pediatric posterior fossa tumor resection", J Neurosurg Pediatr, 27, pp.566~571 (2021)
- Chen JQ, "Strategy for facial nerve management during surgical removal of benign jugular foramen tumors : outcomes and indications", Eur Ann Otorhinolaryngol Head Neck Dis, 136(3S), pp.S21~S25 (2019)
- Odat H, "Facial nerve management in jugular paraganglioma surgery : a literature review", J Laryngol Otol, 130, pp.219~224 (2016)