Millare G G, Guha-Thakurta N, Sturgis E M, El-Naggar A K, Debnam J M
From the Department of Diagnostic Radiology (G.G.M.), Baylor College of Medicine, Houston, Texas.
AJNR Am J Neuroradiol. 2014 Feb;35(2):373-8. doi: 10.3174/ajnr.A3650. Epub 2013 Aug 1.
Dermatofibrosarcoma protuberans is a rare, locally aggressive sarcoma of the skin in children and adults, usually involving the trunk and extremities and less commonly the head and neck. Despite clinical reports in the literature on the management of dermatofibrosarcoma protuberans, there are limited articles describing its imaging features.
We retrospectively reviewed the demographics and imaging findings in all 24 patients with pathologically proven dermatofibrosarcoma protuberans of the head and neck seen at a tertiary cancer center between 2001 and 2010.
Twenty-two of the 24 lesions were nodular and well circumscribed; 19 of the 24 were located on the scalp. On imaging, all 24 lesions involved subcutaneous tissues. The lesions ranged in size from 0.6-9.5 cm (mean, 3.7 cm; standard deviation, 2.3 cm). Twelve lesions involved the soft tissues either at or extending directly to the midline. Thirteen lesions were associated with bulging of the skin surface. Fourteen lesions were imaged with CT and 14 with MR imaging. Whereas variable enhancement patterns were noted on CT and MR imaging, dermatofibrosarcoma protuberans was usually T2-hyperintense and demonstrated marked enhancement. None of the lesions was associated with bone invasion, perineural spread, or nodal/distant metastasis.
Knowledge of the imaging characteristics of dermatofibrosarcoma protuberans may alert neuroradiologists to include dermatofibrosarcoma protuberans in the differential diagnosis of lesions about the head and neck with similar imaging characteristics.
隆突性皮肤纤维肉瘤是一种罕见的、局部侵袭性的皮肤肉瘤,可发生于儿童和成人,通常累及躯干和四肢,较少累及头颈部。尽管文献中有关于隆突性皮肤纤维肉瘤治疗的临床报道,但描述其影像学特征的文章有限。
我们回顾性分析了2001年至2010年间在一家三级癌症中心就诊的所有24例经病理证实的头颈部隆突性皮肤纤维肉瘤患者的人口统计学资料和影像学表现。
24个病灶中有22个呈结节状,边界清晰;24个病灶中有19个位于头皮。影像学检查显示,所有24个病灶均累及皮下组织。病灶大小为0.6 - 9.5 cm(平均3.7 cm;标准差2.3 cm)。12个病灶累及中线处或直接延伸至中线的软组织。13个病灶伴有皮肤表面隆起。14个病灶行CT检查,14个病灶行MR成像检查。虽然CT和MR成像上可见不同的强化模式,但隆突性皮肤纤维肉瘤通常在T2加权像上呈高信号,并表现为明显强化。所有病灶均未伴有骨质侵犯、神经周围扩散或淋巴结/远处转移。
了解隆突性皮肤纤维肉瘤的影像学特征可能会提醒神经放射科医生,在对头颈部具有相似影像学特征的病变进行鉴别诊断时应考虑隆突性皮肤纤维肉瘤。