Department of Ultrasound, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Medicine (Baltimore). 2023 Dec 15;102(50):e36626. doi: 10.1097/MD.0000000000036626.
Myxofibrosarcoma most commonly arises as a slowly enlarging, painless mass. We describe an unusual case of low-grade myxofibrosarcoma in the axillary fossa, which infiltrated the brachial plexus, axillary artery, and axillary vein, causing severe pain. The low incidence and complex anatomical structure make imaging examination and surgery face great challenges. To the best of our knowledge, such presentation of a low-grade myxofibrosarcoma that showed an extreme infiltrative growth pattern and presented severe pain has not been reported before.
We reported a case of low-grade myxofibrosarcoma developed around the axillary neurovascular bundle, with multiple peripheral metastases in an 87-year-old male. Physical examination revealed a mass on the right axillary fossa measuring 5 × 4 cm. The patient underwent computed tomography but no definite diagnosis was obtained. Because he had claustrophobia and could not perform MRI examination. Thus, he underwent conventional ultrasound and contrast-enhanced ultrasound. Ultrasonic examination not only accurately determines the invasion scope of the tumor, but also clearly shows that the nerve has suffered from the invasion of the exogenous tumor and multiple metastatic foci around it. The contrast enhancement mode of the tumor showed centripetal high-enhancement, uneven internal enhancement, visible enhanced bridge, and non-enhancing central area.
Combined with the results of conventional ultrasound and contrast-enhanced ultrasound, we highly suspected it to be soft tissue sarcoma, giving strong clinical assistance.
Given the risk of sarcoma implantation along the needle track and the underestimation of tumor malignancy, an excisional biopsy was considered the most practical choice to avoid unnecessary pain and potential implantation.
The patient underwent surgery and a histopathological examination of the lesion confirmed it as low-grade myxofibrosarcoma.
This report describes a rare case of myxofibrosarcoma of the axillary fossa. High-resolution ultrasound is increasingly used for the initial assessment of soft-tissue masses. However, there are few reports about the ultrasound and contrast-enhanced ultrasound examinations of myxofibrosarcoma. Accurate preoperative diagnosis and proper treatment strategies are critical in managing patients with myxofibrosarcoma. Our case may provide diagnosis experiences and will help better understand and treat this disease.
黏液纤维肉瘤最常表现为缓慢增大、无痛性肿块。我们描述了一例腋腔低度黏液纤维肉瘤的不典型病例,该肿瘤浸润臂丛神经、腋动脉和腋静脉,引起严重疼痛。由于发病率低和解剖结构复杂,影像学检查和手术均面临巨大挑战。据我们所知,此前尚未报道过表现出极端浸润性生长模式并伴有严重疼痛的低度黏液纤维肉瘤病例。
我们报告了一例 87 岁男性腋血管神经束周围发生的低度黏液纤维肉瘤病例,其周围有多个外周转移灶。体格检查发现右腋窝有一个 5×4cm 的肿块。患者行计算机断层扫描(CT)检查,但未明确诊断。由于患者有幽闭恐惧症,无法进行磁共振成像(MRI)检查,因此仅行常规超声和超声造影检查。超声检查不仅能准确判断肿瘤的侵袭范围,还能清晰显示神经已受到外生肿瘤的侵袭及周围多个转移灶。肿瘤的超声造影增强模式表现为向心性高增强、不均匀的内部增强、可见增强桥及无增强的中央区域。
结合常规超声和超声造影结果,我们高度怀疑为软组织肉瘤,为临床提供了有力的辅助诊断。
鉴于肉瘤种植沿针道的风险和肿瘤恶性程度的低估,考虑到避免不必要的疼痛和潜在种植的风险,单纯的病灶切除术是最实用的选择。
患者接受了手术,病变的组织病理学检查结果证实为低度黏液纤维肉瘤。
本报告描述了一例罕见的腋腔黏液纤维肉瘤病例。高分辨率超声越来越多地用于软组织肿块的初步评估。然而,关于黏液纤维肉瘤的超声和超声造影检查的报道较少。准确的术前诊断和适当的治疗策略对黏液纤维肉瘤患者的管理至关重要。我们的病例可能提供了一些诊断经验,并有助于更好地理解和治疗这种疾病。