Department of Surgical Pathology, Medicine, Molecular and Critical Area, University of Pisa, Pisa, Italy.
Department of Surgical Pathology, Medicine, Molecular and Critical Area, University of Pisa, Pisa, Italy.
Oral Surg Oral Med Oral Pathol Oral Radiol. 2021 Feb;131(2):e52-e58. doi: 10.1016/j.oooo.2020.03.053. Epub 2020 Jun 2.
Myxomas are rare benign mesenchymal soft tissue tumors that seldom affect the head and neck area. The present report describes a rare case of intramuscular myxoma of the oral cavity and briefly reviews the literature regarding the occurrence of these lesions in the maxillofacial area.
A 59-year-old patient was referred for the development of a slow-growing tumefaction in the right buccal mucosa in the previous 12 months. Magnetic resonance imaging was performed to characterize the lesion's dimensions and its relationship with the surrounding structures, and it revealed intramuscular localization in correspondence with the medial pterygoid muscle. Incisional biopsy was carried out to aid in the final diagnosis.
Histology revealed the presence of an intramuscular myxoma, characterized by discontinuous margins and locally infiltrating muscular fibers. A second surgery was performed to totally remove the lesion. Follow-up at 6 months did not show any signs of recurrence. A literature search was performed to retrieve data on the incidence of oral intramuscular myxomas.
To the best of our knowledge, this is the first case of intramuscular myxoma of the medial pterygoid muscle reported in the literature. Although rarely encountered, intramuscular myxomas should be considered when performing differential diagnoses of soft tissue masses at the level of the masticatory muscles.
黏液瘤是一种罕见的良性间叶软组织肿瘤,很少影响头颈部。本报告描述了一例口腔内肌内黏液瘤的罕见病例,并简要回顾了这些病变在颌面区域发生的文献。
一名 59 岁患者因 12 个月前右侧颊黏膜出现缓慢生长的肿块而就诊。进行磁共振成像以描述病变的大小及其与周围结构的关系,结果显示位于翼内肌内的肌内定位。进行切开活检以辅助最终诊断。
组织学显示存在肌内黏液瘤,其特征为不连续的边界和局部浸润的肌肉纤维。进行了第二次手术以完全切除病变。6 个月的随访未显示任何复发迹象。进行了文献检索以获取口腔内肌内黏液瘤发病率的数据。
据我们所知,这是首例文献报道的翼内肌肌内黏液瘤。尽管很少见,但在咀嚼肌水平的软组织肿块进行鉴别诊断时应考虑肌内黏液瘤。