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腹膜后丛状神经纤维瘤:CT表现

Retroperitoneal plexiform neurofibromas: CT findings.

作者信息

Bass J C, Korobkin M, Francis I R, Ellis J H, Cohan R H

机构信息

Department of Radiology, University of Michigan Hospitals, Ann Arbor 48109-0030.

出版信息

AJR Am J Roentgenol. 1994 Sep;163(3):617-20. doi: 10.2214/ajr.163.3.8079855.

Abstract

OBJECTIVE

CT findings in retroperitoneal plexiform neurofibromas have been described previously only in a few case reports. This study was performed to characterize the CT features in a larger group of patients with this benign neoplasm and to delineate those findings that suggest the presence of concurrent malignant tumors of the nerve sheath.

MATERIALS AND METHODS

From a review of CT scans showing retroperitoneal masses in 25 patients with neurofibromatosis type 1, we identified 16 patients whose clinical and CT features suggested the diagnosis of plexiform neurofibromas. The diagnosis was confirmed by biopsy of the mass in three patients. In the remaining 13 patients, the diagnosis was supported by long-term follow-up in eight and by biopsy confirmation of either a neurofibroma or a plexiform neurofibroma elsewhere in the body in the other five patients. Concurrent retroperitoneal malignant tumors of the nerve sheath were confirmed by biopsy in five patients.

RESULTS

CT showed bilateral, remarkably symmetric masses extending along the medial and posterior aspects of the psoas muscles in 15 of the 16 patients. Parapsoas masses tended to be long and cylindrical. In addition to parapsoas masses, eight patients had bilateral, symmetric masses extending along the anterior aspect of the sacrum in a sheetlike fashion. Masses were identified in the region of the celiac axis and the origin of the superior mesenteric artery in four patients. Only one patient had an isolated celiac/superior mesenteric artery mass without associated parapsoas or presacral masses. Retroperitoneal masses were of homogeneous, low attenuation when compared with adjacent muscle on CT images of 14 patients. Two patients had an unusual swirling and serpiginous pattern of increased attenuation superimposed on a low-attenuation background. Asymmetry in size and attenuation was due to malignant nerve sheath tumors in five patients.

CONCLUSION

Retroperitoneal plexiform neurofibromas have a characteristic appearance on CT scans. They are typically bilateral, symmetric, low-attenuation masses in a parapsoas or presacral location. Asymmetry in size and attenuation of a larger mass suggests the possibility of a malignant tumor of the nerve sheath. Recognition of the CT features of a retroperitoneal plexiform neurofibroma can obviate the expense, pain, and risk of an unnecessary biopsy. Conversely, detection of findings suggestive of malignant tumor can lead to appropriate recommendation of biopsy.

摘要

目的

此前仅在少数病例报告中描述过腹膜后丛状神经纤维瘤的CT表现。本研究旨在明确一大组患有这种良性肿瘤的患者的CT特征,并描绘出提示同时存在神经鞘恶性肿瘤的表现。

材料与方法

通过回顾25例1型神经纤维瘤病患者显示腹膜后肿块的CT扫描,我们确定了16例临床和CT特征提示丛状神经纤维瘤诊断的患者。3例患者通过肿块活检确诊。其余13例患者中,8例通过长期随访得到支持,另外5例通过身体其他部位神经纤维瘤或丛状神经纤维瘤的活检确诊。5例患者通过活检确诊同时存在腹膜后神经鞘恶性肿瘤。

结果

16例患者中有15例CT显示双侧明显对称的肿块沿腰大肌内侧和后侧延伸。腰大肌旁肿块往往呈长圆柱形。除腰大肌旁肿块外,8例患者有双侧对称的肿块以片状形式沿骶骨前方延伸。4例患者在腹腔干和肠系膜上动脉起源区域发现肿块。只有1例患者有孤立的腹腔干/肠系膜上动脉肿块,无相关的腰大肌旁或骶前肿块。与相邻肌肉相比,14例患者的CT图像上腹膜后肿块呈均匀低密度。2例患者在低密度背景上有不寻常的漩涡状和匐行状强化模式。5例患者的大小和密度不对称是由于恶性神经鞘肿瘤。

结论

腹膜后丛状神经纤维瘤在CT扫描上有特征性表现。它们通常是双侧对称的低密度肿块,位于腰大肌旁或骶前。较大肿块的大小和密度不对称提示神经鞘恶性肿瘤的可能性。认识腹膜后丛状神经纤维瘤的CT特征可以避免不必要活检的费用、痛苦和风险。相反,发现提示恶性肿瘤的表现可导致适当的活检建议。

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