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A pilot evaluation of magnetic resonance imaging characteristics seen with solid papillary carcinomas of the breast in 4 patients

BACKGROUND: Solid papillary carcinoma (SPC) is a rare variant of breast papillary carcinoma with unique pathological morphology and biological behavior. There is only one case report on T(1)-MRI of SPC. In this study, we report our findings on this new category of papillary carcinoma to fill the gap...

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Detalles Bibliográficos
Autores principales: Zhang, Lina, Zhuang, Ling, Shi, Chang, Miao, Yanwei, Zhang, Weisheng, Song, Qingwei, Kang, Jianyun, Lang, Zhijin, Xin, Xuegang, Liu, Ailian, Hu, Jiani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547522/
https://www.ncbi.nlm.nih.gov/pubmed/28784112
http://dx.doi.org/10.1186/s12885-017-3518-8
Descripción
Sumario:BACKGROUND: Solid papillary carcinoma (SPC) is a rare variant of breast papillary carcinoma with unique pathological morphology and biological behavior. There is only one case report on T(1)-MRI of SPC. In this study, we report our findings on this new category of papillary carcinoma to fill the gap in MRI characterization of SPC. METHODS: This retrospective study included four pathology-confirmed in situ SPC patients. Conventional MRI, diffusion weighted imaging (DWI), and magnetic resonance spectroscopy (MRS) were performed with a 1.5 T whole-body MR scanner before surgical operation. The following characteristics of each lesion were recorded: signal intensity on T(2)WI/STIR and T(1)FSPGR, morphology, maximum lesion size, and time intensity curve (TIC) on dynamic contrast enhancement MRI (DCE-MRI), apparent diffusion coefficient (ADC) value from DWI, and Cho peak from MRS. RESULTS: Signal intensities of all lesions were heterogenous on T(2)WI/STIR and T(1)FSPGR. Mass enhancements were observed for all lesions with either oval or irregular shapes on DCE-MRI. The maximum lesion size ranged from 0.8 cm to 3.2 cm. All lesion margins were circumscribed, and internal enhancements were homogeneous or heterogeneous from DCE-MRI. TIC appeared with a rapid increase in initial contrast phases of all lesions. All lesions on DWI (b = 1000s/mm(2)) were slightly hyperintense with an ADC value range of 1.3 × 10(−3) mm(2)/s to 1.9 × 10(−3) mm(2)/s. Cho peak was absent at 3.2 ppm for all lesions. CONCLUSIONS: MRI characteristics of SPC include heterogeneous signal intensity within the lesion on T(2)WI/STIR and T(1)FSPGR, mass enhancement with circumscribed margins, either oval or irregular shapes, and a rapid initial enhancement of TIC on DCE-MRI. ADC values and the absence of Cho peak may provide valuable information to distinguish SPC from other invasive breast carcinomas.