Regional Service of Neurosurgery, Hospital Clínico Universitario Virgen de la Arrixaca, El Palmar, Murcia, Spain.
Pathology Department, Hospital Clínico Universitario Virgen de la Arrixaca, El Palmar, Murcia, Spain.
Oper Neurosurg (Hagerstown). 2018 Apr 1;14(4):325-340. doi: 10.1093/ons/opx149.
Arteriovenous malformations of the temporalis muscle (TM-AVMs) are rare lesions commonly considered as a variant of scalp AVMs. A study was designed in order to analyze TM-AVMs features and to confirm them as a certain entity different from scalp AVMs. Seven TM-AVMs cases (5 from literature plus 2 from our database) were studied. Clinical, epidemiological, radiological, and therapeutic data were analyzed and compared to common scalp AVMs features. All TM-AVMs presented as large soft tumor-like masses on the temporal region (mean diameter: 6 cm). Pain was referred in half of cases, while overlying cutaneous stigmas were described only once. No masticatory malfunction was reported. TM-AVMs tend to appear in young patients (mean: 29 yr), commonly as longstanding and slow-evolving lesions (mean evolution time before diagnosis: 5 yr). All cases displayed a diffuse slow-flow blush on angiogram. All TM-AVMs were completely located within the TM, with no involvement of scalp or bone. The pathological analysis of all cases demonstrated the presence of striate muscular bundles intermingled with fairly mature arterial and venous vessels. No clearly distorted vessel was found within the TM-AVMs. Surgery was performed for all cases with complete removal. Preoperative embolization was done in 4 cases to reduce blood loss during surgery. No clinical/radiological recurrence was reported. Opposite to TM-AVMs, scalp AVMs commonly present as high-flow lesions with no evident tumor mass, mainly located in the subcutaneous tissue. TM-AVMs present clearly distinct features compared to scalp AVMs, for which they should be considered as a certain pathological entity and not as a variant of scalp AVMs.
颞肌动静脉畸形(TM-AVM)是一种罕见的病变,通常被认为是头皮 AVM 的一种变体。本研究旨在分析 TM-AVM 的特征,并证实其为一种与头皮 AVM 不同的特定实体。研究了 7 例 TM-AVM 病例(5 例来自文献,2 例来自我们的数据库)。分析了临床、流行病学、影像学和治疗数据,并与常见的头皮 AVM 特征进行了比较。所有 TM-AVM 均表现为颞区的大软瘤样肿块(平均直径:6cm)。半数病例有疼痛,仅一次描述了皮上标记。未报告咀嚼功能障碍。TM-AVM 倾向于出现在年轻患者(平均年龄:29 岁),通常是长期缓慢进展的病变(平均诊断前进展时间:5 年)。所有病例的血管造影均显示弥漫性缓慢血流充血。所有 TM-AVM 均完全位于 TM 内,无头皮或骨骼受累。所有病例的病理分析均显示存在条纹状肌肉束,混杂着相当成熟的动脉和静脉血管。在 TM-AVM 内未发现明显扭曲的血管。所有病例均行手术切除,4 例行术前栓塞以减少术中失血。无临床/影像学复发。与 TM-AVM 相反,头皮 AVM 通常表现为高流量病变,无明显肿瘤肿块,主要位于皮下组织。TM-AVM 与头皮 AVM 相比具有明显不同的特征,应将其视为一种特定的病理实体,而不是头皮 AVM 的变体。