Lee Justin C, Thomas J Meirion, Phillips Simon, Fisher Cyril, Moskovic Eleanor
Department of Radiology, Chelsea and Westminster Hospital, 369 Fulham Road, London SW10 9NH, England.
AJR Am J Roentgenol. 2006 Jan;186(1):247-54. doi: 10.2214/AJR.04.1674.
We present the MRI features with pathologic correlation of aggressive fibromatosis, incorporating 203 cases over a 5-year period from the Royal Marsden Hospital Sarcoma Unit database.
Sixty patients had imaging available for retrospective review of which 29 had preoperative MRI and final histopathologic diagnosis of aggressive fibromatosis.
The average age at diagnosis was 41.3 years with a female-to-male sex ratio of 1.2:1. Twenty lesions were extraabdominal; six, intraabdominal; and three, in the abdominal wall (classic desmoid). The average tumor size was 6.4 cm (range, 2.2-13.7 cm). Intraabdominal aggressive fibromatosis produced the largest tumors, averaging 9.5 cm. Most lesions were ovoid (52%) or infiltrative (34.5%) in outline with an irregular or lobulated contour (76%). The lesions crossed major fascial boundaries in 31% of cases overall and in 66% of patients referred for recurrent disease. On MRI, homogeneous isointensity or mild hyperintensity on T1-weighted images and heterogenous high signal on T2-weighted or STIR images were seen. All lesions enhanced after IV gadolinium, usually avidly. In contrast to previous reports, 38% of cases failed to show low signal on all pulse sequences and no abnormalities were seen in local bone structures. Histology showed sheets of bland spindle cells in dense collagen and did not vary with the MRI signal characteristics of the lesion. Patients referred for recurrent disease were most likely to have a recurrence after surgery. MRI and pathology findings did not predict recurrence.
Accurate diagnosis and staging of aggressive fibromatosis by MRI have important treatment and prognostic implications.
我们展示侵袭性纤维瘤病的MRI特征及其与病理的相关性,纳入了皇家马斯登医院肉瘤科数据库5年期间的203例病例。
60例患者有影像学资料可供回顾性分析,其中29例术前行MRI检查并最终经组织病理学诊断为侵袭性纤维瘤病。
诊断时的平均年龄为41.3岁,女性与男性的性别比为1.2:1。20个病变位于腹外;6个位于腹内;3个位于腹壁(典型硬纤维瘤)。肿瘤平均大小为6.4 cm(范围2.2 - 13.7 cm)。腹内侵袭性纤维瘤病产生的肿瘤最大,平均为9.5 cm。大多数病变轮廓呈卵圆形(52%)或浸润性(34.5%),轮廓不规则或呈分叶状(76%)。总体上31%的病例病变跨越主要筋膜边界,而在因复发性疾病转诊的患者中这一比例为66%。在MRI上,T1加权像呈均匀等信号或轻度高信号,T2加权像或短反转恢复序列(STIR)像呈不均匀高信号。所有病变静脉注射钆剂后均强化,通常强化明显。与既往报道不同,38%的病例在所有脉冲序列上均未显示低信号,局部骨结构未见异常。组织学显示密集胶原中可见成片的温和梭形细胞,且与病变的MRI信号特征无关。因复发性疾病转诊的患者术后最易复发。MRI和病理结果均不能预测复发。
通过MRI对侵袭性纤维瘤病进行准确诊断和分期对治疗及预后具有重要意义。