Three cases of sporadic meningioangiomatosis with different imaging appearances: case report and review of the literature

被引:14
作者
Sun, Zhihua [1 ]
Jin, Fei [1 ]
Zhang, Jing [1 ]
Fu, Yue [1 ]
Li, Wei [1 ]
Guo, Hong [1 ]
Zhang, Yunting [1 ]
机构
[1] Tianjin Med Univ, Gen Hosp, Dept Radiol, Tianjin 300052, Peoples R China
基金
中国国家自然科学基金;
关键词
Meningioangiomatosis; Magnetic resonance imaging; Flow void effect; Cystic meningioangiomatosis; BRAIN; MENINGIOMA;
D O I
10.1186/s12957-015-0477-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Meningioangiomatosis (MA) is a rare meningiovascular malformation or hamartomatous lesion in the central nervous system. Radiographic findings of MA may show a variety of characteristics according to different histological components. We present three cases of sporadic MA with different imaging appearances in an attempt to identify specific imaging characteristics. Case presentation: In case 1, an irregular hyperdense solid mass was localized in the left middle cranial fossa, demonstrating low and equal signal intensity on T1-weighted imaging (T1WI; TR/TE 2,048.9 ms/26.1 ms), high signal intensity with multiple flow void effect on T2-weighted imaging (T2WI; TR/TE 4,000 ms/106.4 ms), and significant and homogeneous enhancement on post-contrast magnetic resonance imaging (MRI). In case 2, the lesion in the right insular lobe showed a cystic-mural nodule pattern. The cystic content demonstrated similar density or signal intensity as cerebrospinal fluid, while the mural nodule demonstrated equal density or signal intensity on computed tomography (CT) and MRI. On post-contrast MRI, the mural nodule showed significant enhancement, but the cystic wall and content showed no enhancement. In case 3, a remarkably enhanced solid nodule was found in the cortex of the left parietal lobe with multiple small cysts surrounding it. This nodule showed low signal intensity on T2WI and diffusion-weighted imaging (DWI; TR/TE 6,000 ms/96.8 ms, b = 1,000 s/mm(2)). The preoperative diagnoses of the above three cases were meningioma, hemangioblastoma, and ganglioglioma. However, all were pathologically diagnosed as MA. Conclusion: The presented cases demonstrate that MA may present with solid and cystic imaging patterns, which may include large cystic-mural nodules and small intra-and extra-cystic patterns. Although MA imaging diagnoses are difficult, several MRI signs may include specific characteristics, such as a flow void effect on T2WI and separating cysts in the cystic MA (as shown in our cases), gyriform hyperintensity on T2-fluid attenuated inversion recovery (FLAIR) sequence, and susceptibility artifacts on T2 gradient echo (GRE) sequences (as found in the literature).
引用
收藏
页数:6
相关论文
共 25 条
[1]   Meningioangiomatosis in a patient with progressive focal neurological deficit-case report and review of literature [J].
Abdulazim, A. ;
Zella, M. A. Samis ;
Rapp, M. ;
Gierga, K. ;
Langen, K. J. ;
Steiger, H. J. ;
Sabel, M. .
BRITISH JOURNAL OF NEUROSURGERY, 2013, 27 (02) :253-255
[2]  
Arcos A, 2010, NEUROCIRUGIA, V21, P461
[3]   Report of a case of central and peripheral neurofibromatosis [J].
Bassoe, P ;
Nuzum, F .
JOURNAL OF NERVOUS AND MENTAL DISEASE, 1915, 42 :785-796
[4]   Sporadic meningioangiomatosis-associated atypical meningioma mimicking parenchymal invasion of brain: a case report and review of the literature [J].
Chen, Yan-yang ;
Tiang, Xiao-ying ;
Li, Zhi ;
Luo, Bo-ning ;
Huang, Quan .
DIAGNOSTIC PATHOLOGY, 2010, 5
[5]  
Fedi M, 2009, Br J Radiol, V82, pe129, DOI 10.1259/bjr/56536580
[6]   Diagnosis and surgical treatment of sporadic meningioangiomatosis [J].
Feng, Rui ;
Hu, Jie ;
Che, Xiaoming ;
Pan, Li ;
Wang, Zhiqiu ;
Zhang, Mingguang ;
Huang, Fengping ;
Xu, Bin ;
Mao, Renting ;
Sun, An ;
Bao, Weimin ;
Zhong, Ping ;
Wang, Yin .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2013, 115 (08) :1407-1414
[7]   Meningioangiomatosis: A Case Report and Literature Review Emphasizing Diverse Appearance on Different Imaging Modalities [J].
Kashlan, Osama N. ;
LaBorde, David V. ;
Davison, LaKesha ;
Saindane, Amit M. ;
Brat, Daniel ;
Hudgins, Patricia A. ;
Gross, Robert E. .
CASE REPORTS IN NEUROLOGICAL MEDICINE, 2011, 2011
[8]   Allelic loss on chromosomes 1p32, 9p21, 13q14, 16q22, 17p, and 22q12 in meningiomas associated with meningioangiomatosis and pure meningioangiomatosis [J].
Kim, Na Rae ;
Cho, Seong Jin ;
Suh, Yeon-Lim .
JOURNAL OF NEURO-ONCOLOGY, 2009, 94 (03) :425-430
[9]   A Case of Infantile Meningioangiomatosis with a Separate Cyst [J].
Kim, Seong Ho ;
Yoon, Soo Han ;
Kim, Jang Hee .
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY, 2009, 46 (03) :252-256
[10]   Meningioangiomatosis: MR imaging and pathological correlation in two cases [J].
Kim, WY ;
Kim, IO ;
Kim, WS ;
Cheon, JE ;
Yeon, KM .
PEDIATRIC RADIOLOGY, 2002, 32 (02) :96-98