Department of Radiology, Facultad de Medicina, Clínica Alemana de Santiago, Universidad del Desarrollo, Santiago, Chile.
Departamento de Dermatología, Clínica Alemana de Santiago, Santiago, Chile.
J Ultrasound. 2024 Mar;27(1):61-65. doi: 10.1007/s40477-023-00796-2. Epub 2023 Jul 14.
Dermatofibrosarcoma protuberans (DFSP) is a low-grade spindle cell sarcoma of fibroblastic origin. This tumor originates in the dermis and infiltrates the subcutaneous tissue. The highest incidence occurs in the third and fourth decades of life, affecting most frequently the trunk and proximal extremities. Ultrasound is performed in those cases where the clinical appearance of the lesion is not typical and when the physician wants to determine the extent and depth of the lesion.
Retrospective analysis of the ultrasound and demographic findings of thirteen patients with DFSP.
13 patients, 8 females and 5 males, aged from 2 months to 58 years old. One patient with two different separated synchronous tumors. On ultrasonography they compromised the dermal hypodermal layers in 93% of the cases and 1 dermal lesion. The compromise reached the aponeurotic plane in two cases. The sized varied from 5 to 38 mm. They presented as a well-defined hypoechogenic nodule in seven cases (50%). In three cases (21%) they presented as a hypoechogenic infiltrate ill-defined border solid lesion; in two cases as a plaque ill-defined lesion, and two cases as a pseudonodular inflammatory lesion with irregular borders. All lesions appeared vascularized on color Doppler imaging.
DFSP is a low grade sarcoma of fibroblastic origin, that usually arises in the dermis and infiltrates the subcutaneous tissue. The clinical presentations are variable. On ultrasound we found different patterns: well-defined hypoechogenic solid nodule, hypoechogenic infiltrate ill-defined border solid lesion, plaque ill-defined lesion, and pseudonodular inflammatory lesion. It is important to know and recognize this suspicious different ultrasound presentations in order to recommend a histological study.
隆突性皮肤纤维肉瘤(DFSP)是一种起源于成纤维细胞的低度 spindle 细胞肉瘤。这种肿瘤起源于真皮并浸润皮下组织。发病率最高的年龄在 30 到 40 岁之间,最常影响躯干和近端肢体。当病变的临床表现不典型或医生希望确定病变的范围和深度时,会进行超声检查。
回顾性分析 13 例 DFSP 患者的超声和人口统计学资料。
13 例患者,8 例女性,5 例男性,年龄从 2 个月到 58 岁。1 例患者有两个不同的、分开的、同步的肿瘤。在超声检查中,它们在 93%的病例中累及真皮-皮下层,在 1 例中累及真皮病变。在 2 例中累及腱膜平面。病变大小从 5 到 38 毫米不等。7 例(50%)表现为边界清晰的低回声结节。3 例(21%)表现为边界不清的低回声浸润性实性病变;2 例表现为斑块状边界不清的病变,2 例表现为边界不规则的假结节性炎症性病变。所有病变在彩色多普勒成像上均显示为血管化。
DFSP 是一种起源于成纤维细胞的低度肉瘤,通常起源于真皮并浸润皮下组织。临床表现多样。在超声检查中,我们发现了不同的表现模式:边界清晰的低回声实性结节、边界不清的低回声浸润性实性病变、斑块状边界不清的病变和边界不规则的假结节性炎症性病变。了解并识别这些可疑的不同超声表现对于推荐进行组织学研究很重要。