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胸部Castleman病:影像学特征与临床及组织病理学对照

Castleman disease of the thorax: radiologic features with clinical and histopathologic correlation.

作者信息

McAdams H P, Rosado-de-Christenson M, Fishback N F, Templeton P A

机构信息

Department of Radiology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Radiology. 1998 Oct;209(1):221-8. doi: 10.1148/radiology.209.1.9769835.

DOI:10.1148/radiology.209.1.9769835
PMID:9769835
Abstract

PURPOSE

To correlate the radiologic manifestations of thoracic Castleman disease with the clinical and histopathologic features.

MATERIALS AND METHODS

The clinical, surgical, and histopathologic records; chest radiographs; and computed tomographic (CT) and magnetic resonance (MR) images in 30 pathologically proved cases of thoracic Castleman disease were reviewed.

RESULTS

Patients with localized Castleman disease (n = 24) typically had the hyaline-vascular type (n = 23), were asymptomatic (n = 14), and had solitary, well-circumscribed mediastinal masses (n = 24). All lesions at contrast material-enhanced CT (n = 13) enhanced. All lesions at MR imaging (n = 5) were heterogeneous and had increased signal intensity on T1- and T2-weighted images. Three patterns were observed on CT or MR images in 20 patients: a solitary, noninvasive mass (n = 10); a dominant infiltrative mass with associated lymphadenopathy (n = 8); or matted lymphadenopathy without a dominant mass (n = 2). Patients with disseminated Castleman disease (n = 6) typically had the plasma cell type (n = 4), were symptomatic at presentation (n = 5), and had bilateral mediastinal masses on chest radiographs (n = 4). At CT, all lesions manifested with diffuse mediastinal lymphadenopathy. All lesions at contrast-enhanced CT (n = 5) enhanced.

CONCLUSION

Localized Castleman disease manifests as either a solitary, well-circumscribed mediastinal mass or an infiltrative mass with associated lymphadenopathy on CT or MR images. Disseminated Castleman disease manifests with diffuse mediastinal lymphadenopathy.

摘要

目的

将胸内Castleman病的放射学表现与临床及组织病理学特征进行关联。

材料与方法

回顾了30例经病理证实的胸内Castleman病患者的临床、手术及组织病理学记录、胸部X线片、计算机断层扫描(CT)和磁共振(MR)图像。

结果

局限性Castleman病患者(n = 24)通常为透明血管型(n = 23),无症状(n = 14),有孤立的、边界清晰的纵隔肿块(n = 24)。对比增强CT上的所有病变(n = 13)均有强化。MR成像上的所有病变(n = 5)均不均匀,在T1加权和T2加权图像上信号强度增加。20例患者的CT或MR图像上观察到三种模式:孤立的、非侵袭性肿块(n = 10);伴有相关淋巴结病的主要浸润性肿块(n = 8);或无主要肿块的融合淋巴结病(n = 2)。播散性Castleman病患者(n = 6)通常为浆细胞型(n = 4),就诊时出现症状(n = 5),胸部X线片显示双侧纵隔肿块(n = 4)。CT上,所有病变均表现为弥漫性纵隔淋巴结肿大。对比增强CT上的所有病变(n = 5)均有强化。

结论

局限性Castleman病在CT或MR图像上表现为孤立的、边界清晰的纵隔肿块或伴有相关淋巴结病的浸润性肿块。播散性Castleman病表现为弥漫性纵隔淋巴结肿大。

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