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侵袭性血管黏液瘤:全面的影像学综述,结合临床和组织病理学相关性。

Aggressive angiomyxomas: a comprehensive imaging review with clinical and histopathologic correlation.

机构信息

1 Department of Radiology, The University of Texas Health Science Center at Houston, 6431 Fannin St, MSB 2.130, Houston, TX 77030.

出版信息

AJR Am J Roentgenol. 2014 Jun;202(6):1171-8. doi: 10.2214/AJR.13.11668.

Abstract

OBJECTIVE

Aggressive angiomyxomas are rare infiltrative mesenchymal neoplasms that commonly recur locally. The purpose of this study was to conduct a retrospective review of imaging findings of aggressive angiomyxomas with clinicopathologic correlation in 16 patients.

MATERIALS AND METHODS

CT and MRI studies and clinical data of 16 patients with histopathologic evidence of aggressive angiomyxoma who had been referred to our institutions from January 2002 through January 2012 were retrospectively reviewed. The tumors were evaluated with respect to location, morphology, attenuation or signal intensity, and enhancement characteristics.

RESULTS

The most common location was the pelvis and perineum with the mass on either side of the pelvic diaphragm (12/16, 75%). The characteristic "laminated" appearance was seen in 10 of 12 patients on MRI. Aggressive angiomyxomas showed only mild diffusion restriction and mild (18)F-FDG avidity in both of the two patients who underwent DWI and PET/CT, in keeping with histologic low-mitotic activity. Imaging features, such as collateral vessels and fingerlike growth pattern, were seen in seven of 16 (44%) aggressive angiomyxomas. Internal cystic degeneration was seen in three of 16 (19%) aggressive angiomyxomas.

CONCLUSION

The finding of a large multicompartmental tumor with a characteristic internal laminated morphology or extension on either side of the pelvic diaphragm should alert the radiologist to the possible diagnosis of aggressive angiomyxoma. Imaging features, such as large peripheral vessels and cystic degeneration are less common, but presence of these features in the background of laminated morphology should not deter the radiologist from suggesting a diagnosis of aggressive angiomyxoma.

摘要

目的

侵袭性血管黏液瘤是一种罕见的浸润性间叶性肿瘤,常局部复发。本研究的目的是对 16 例侵袭性血管黏液瘤患者的影像学表现进行回顾性分析,并与临床病理进行相关性分析。

材料与方法

回顾性分析 2002 年 1 月至 2012 年 1 月期间我院收治的 16 例经组织病理学证实为侵袭性血管黏液瘤患者的 CT 和 MRI 表现及临床资料。评估肿瘤的位置、形态、衰减或信号强度及强化特征。

结果

最常见的部位是骨盆和会阴,肿瘤位于骨盆膈的两侧(12/16,75%)。12 例患者中有 10 例 MRI 显示出特征性的“分层”外观。在 2 例行 DWI 和 PET/CT 的患者中,侵袭性血管黏液瘤仅表现出轻度弥散受限和轻度(18)F-FDG 摄取,与组织学低有丝分裂活性一致。在 16 例侵袭性血管黏液瘤中,有 7 例(44%)可见侧支血管和指状生长模式等影像学特征。在 16 例侵袭性血管黏液瘤中有 3 例(19%)可见内部囊性变性。

结论

如果发现一个具有特征性内部分层形态或在骨盆膈两侧延伸的大的多房性肿瘤,放射科医生应警惕侵袭性血管黏液瘤的可能诊断。大的外周血管和囊性变性等影像学特征不常见,但在分层形态的背景下存在这些特征不应阻止放射科医生提出侵袭性血管黏液瘤的诊断。

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