Kransdorf M J, Meis-Kindblom J M
Department of Radiology, Saint Mary's Hospital, Richmond, VA 23226.
AJR Am J Roentgenol. 1994 Aug;163(2):391-4. doi: 10.2214/ajr.163.2.8037038.
Dermatofibrosarcoma protuberans is a distinct clinicopathologic entity characterized by fibroblasts with a prominent storiform pattern. It accounts for about 6% of all soft-tissue sarcomas. The lesion is typically superficial, and the diagnosis can be suspected on the basis of the tumor's clinical appearance. Consequently, the imaging appearance of this entity is essentially unreported. Large lesions, however, can infiltrate the deep soft tissue and be confused with higher-grade sarcomas. We report the radiologic appearance in 11 cases of histologically proved dermatofibrosarcoma protuberans.
The radiologic images of 11 patients who had histologically verified dermatofibrosarcoma protuberans were retrospectively studied. The patients included eight males and three females 9-47 years old (mean, 33 years). Each had a soft-tissue mass that had been present for a variable period, from 3 months to 23 years. CT scans were available for review in six cases, MR images in four, radiographs in nine, bone scintigrams in three, and arteriograms in three.
All lesions were unmineralized nodular masses involving the skin and subcutaneous adipose tissue. The size, in greatest dimension on imaging studies, was 3-22 cm. CT scans (six cases) showed a well-defined lesion with a distinct lobular or nodular architecture and tissue attenuation approximately equal to or greater than that of skeletal muscle. Moderate enhancement was seen on CT scans obtained after injection of contrast material. Arteriograms (three cases) showed mild to moderate hypervascularity. The MR appearance (four cases) was nonspecific; the lesions had prolonged T1 and T2 relaxation times. In one case, MR images showed multiple nodular lesions. Radiographs (nine cases) showed a soft-tissue mass or soft-tissue swelling without evidence of bone involvement or calcification. Bone scintigrams (three cases) showed increased accumulation of tracer.
The radiologic appearance of dermatofibrosarcoma protuberans is typically that of an unmineralized, nodular soft-tissue mass involving the skin and subcutaneous adipose tissue. CT scans or MR images are well suited to show this location, the relation of the lesion to underlying structures, and the distinct lobular or nodular architecture. Arteriograms will show mild to moderate hypervascularity and bone scintigrams will show increased accumulation of radiopharmaceutical.
隆突性皮肤纤维肉瘤是一种独特的临床病理实体,其特征为具有显著席纹状结构的成纤维细胞。它约占所有软组织肉瘤的6%。该病变通常位于浅表,根据肿瘤的临床表现可怀疑其诊断。因此,关于该实体的影像学表现基本上未被报道。然而,较大的病变可浸润深部软组织,并与高级别肉瘤相混淆。我们报告11例经组织学证实的隆突性皮肤纤维肉瘤的放射学表现。
对11例经组织学证实为隆突性皮肤纤维肉瘤患者的放射学图像进行回顾性研究。患者包括8名男性和3名女性,年龄9 - 47岁(平均33岁)。每个人都有一个存在不同时间的软组织肿块,从3个月到23年不等。6例患者有CT扫描图像可供回顾,4例有磁共振成像(MR)图像,9例有X线片,3例有骨闪烁显像,3例有动脉造影。
所有病变均为未矿化的结节状肿块,累及皮肤和皮下脂肪组织。影像学检查最大径为3 - 22 cm。CT扫描(6例)显示病变边界清晰,具有明显的小叶状或结节状结构,组织密度约等于或高于骨骼肌。注射对比剂后CT扫描可见中度强化。动脉造影(3例)显示轻度至中度血管增多。MR表现(4例)无特异性;病变T1和T2弛豫时间延长。1例患者的MR图像显示多个结节状病变。X线片(9例)显示软组织肿块或软组织肿胀,无骨受累或钙化证据。骨闪烁显像(3例)显示示踪剂摄取增加。
隆突性皮肤纤维肉瘤的放射学表现通常为累及皮肤和皮下脂肪组织的未矿化结节状软组织肿块。CT扫描或MR图像非常适合显示该病变的位置、与深部结构的关系以及明显的小叶状或结节状结构。动脉造影将显示轻度至中度血管增多,骨闪烁显像将显示放射性药物摄取增加。